PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
9612213-8	1998	A quantitative Western analysis for NHE3 was developed, using as an internal standard a fusion protein of the COOH-terminal 85 amino acids of NHE3 and maltose binding protein.	Maltose	151-158	sodium/hydrogen exchanger 3	Oryctolagus cuniculus	36-40
9436275-5	1997	A rabbit serum made to a synthetic peptide of IFN-gamma immunoprecipitated a 60 kDa E. coli maltose-binding fusion protein of recombinant IFN-gamma (MBP-IFN) and a 26-27 kDa secreted protein from COS cells and Con A-activated spleen cells.	Maltose	92-99	interferon gamma	Gallus gallus	46-55
9413144-1	1997	The thermal stability of enzymes lactase and invertase in dried, amorphous matrices of sugars (trehalose, maltose, lactose, sucrose, raffinose) and some other selected systems (casein, PVP, milk) was studied.	Maltose	106-113	lactase	Homo sapiens	33-40
9523717-2	1998	A kinetic study was carried out on the inhibitory effects of acarbose, maltose, and maltotriose on porcine pancreatic alpha-amylase (PPA), using maltopentaose as the substrate.	Maltose	71-78	amylase alpha 2A	Homo sapiens	107-131
9423878-0	1998	Characterization of the immunostimulatory properties of Leishmania infantum HSP70 by fusion to the Escherichia coli maltose-binding protein in normal and nu/nu BALB/c mice.	Maltose	116-123	heat shock protein 1B	Mus musculus	76-81
9436275-5	1997	A rabbit serum made to a synthetic peptide of IFN-gamma immunoprecipitated a 60 kDa E. coli maltose-binding fusion protein of recombinant IFN-gamma (MBP-IFN) and a 26-27 kDa secreted protein from COS cells and Con A-activated spleen cells.	Maltose	92-99	interferon gamma	Gallus gallus	138-147
9236937-2	1997	A 52 kDa maltose binding-AgB fusion protein (rAgB.MBP) was produced and inclusion bodies containing the fusion protein were solubilised in urea and affinity purified on an amylose-Sepharose 6B column.	Maltose	9-16	Ras-related GTP binding B	Rattus norvegicus	25-28
9236937-2	1997	A 52 kDa maltose binding-AgB fusion protein (rAgB.MBP) was produced and inclusion bodies containing the fusion protein were solubilised in urea and affinity purified on an amylose-Sepharose 6B column.	Maltose	9-16	Ras-related GTP binding B	Rattus norvegicus	45-49
9236937-2	1997	A 52 kDa maltose binding-AgB fusion protein (rAgB.MBP) was produced and inclusion bodies containing the fusion protein were solubilised in urea and affinity purified on an amylose-Sepharose 6B column.	Maltose	9-16	myelin basic protein	Homo sapiens	50-53
9024004-2	1997	It rapidly converted maltose to panose (Glc alpha-->6 Glc alpha l-->4 Glc) with a Vmax value of 5.8 mmol l-1 min-1 at 50 degrees C in 0.05 mol l-1 sodium acetate buffer (pH 4.4).	Maltose	21-28	CD59 molecule (CD59 blood group)	Homo sapiens	115-120
9294435-4	1997	Expressed from the tac promoter, RafY significantly increases the uptake rates for maltose, sucrose, and raffinose at low substrate concentrations; in particular it shifts the apparent K(m) for raffinose transport from 2 mM to 130 microM.	Maltose	83-90	glycoporin	Escherichia coli	33-37
9309217-6	1997	RESULTS: The structures of MBP complexed with maltose, maltotriose and maltotetraose have been refined to high resolutions (1.67 to 1.8 A).	Maltose	46-53	myelin basic protein	Homo sapiens	27-30
9282831-7	1997	The variant human FMO3 cDNA was constructed from wild type human FMO3 cDNA by site-directed mutagenesis as maltose-binding protein fusions.	Maltose	107-114	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	18-22
9282831-8	1997	Five distinct human FMO3 mutants were expressed as fusion proteins in Escherichia coli and compared with wild type human FMO3 maltose-binding proteins (FMO3-MBP) for the N-oxygenation of 10-[(N,N-dimethylamino)pentyl]-2-(trifluoromethyl)phenothiazine, tyramine, and trimethylamine.	Maltose	126-133	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	121-125
9280409-0	1997	Characterization of two human flavin-containing monooxygenase (form 3) enzymes expressed in Escherichia coli as maltose binding protein fusions.	Maltose	112-119	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	30-69
9280409-6	1997	It was found that expression of both lys158 and glu158 enzymes of the human flavin-containing monooxygenase form 3 as fusions with the maltose binding protein resulted in an enzyme that was soluble and greatly stabilized and had a reduced requirement for detergent during enzyme purification and during the assay for activity.	Maltose	135-142	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	76-114
9280409-8	1997	With the exception of the stability and solubility characteristics, the physical and chemical properties of lys158 and glu158 maltose binding fusion proteins of human flavin-containing monooxygenase form 3 variants resembled that of flavin-containing monooxygenase enzyme activity associated with human liver microsomes and enzyme isolated from a previous Escherichia coli expression system that lacked the protein fusion.	Maltose	126-133	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	167-205
9280409-10	1997	Expression of the adult human flavin-containing monooxygenase form 3 as a maltose binding protein has allowed considerable advances over the previously reported cDNA-expressed enzyme systems and may provide the basis for examining the role of the flavin-containing monooxygenase in human xenobiotic or drug metabolism.	Maltose	74-81	flavin containing dimethylaniline monoxygenase 3	Homo sapiens	30-68
9234903-4	1997	The malachite green insulin was also covalently labeled with maltose (MIMG) to provide binding affinity to RuCon A.	Maltose	61-68	insulin	Homo sapiens	20-27
9153228-11	1997	The binding between SP-D and mannan also required the presence of calcium, but this interaction was completely inhibited by maltose.	Maltose	124-131	surfactant protein D	Homo sapiens	20-24
9111074-2	1997	Hexose oxidase from Chondrus crispus catalyzes the oxidation of a variety of mono- and disaccharides including D-glucose, D-galactose, maltose, and lactose.	Maltose	135-142	CHC_T00009130001	Chondrus crispus	0-14
9151960-3	1997	Glucose uptake was below the detection level in the hxt1-7 null strain growing on maltose.	Maltose	82-89	hexose transporter HXT1	Saccharomyces cerevisiae S288C	52-56
9163329-5	1997	The recombinant SP-D was purified on a nickel column and then on a maltose-agarose column.	Maltose	67-74	surfactant protein D	Homo sapiens	16-20
9119501-2	1997	We used the recombinant 56-kDa protein of R. tsutsugamushi Boryong fused with the maltose-binding protein of Escherichia coli (MBP-Bor56) to analyze its ability to induce protective immunity in a C3H/HeDub murine model.	Maltose	82-89	myelin basic protein	Mus musculus	127-130
9060618-7	1997	In this study, we detected two UL15 gene products of 81 and 30 kDa in HSV-1-infected cells, using a polyclonal antibody raised against a maltose binding protein fusion construct containing UL15 exon 2.	Maltose	137-144	DNA packaging terminase subunit 1	Human alphaherpesvirus 1	31-35
9224643-3	1997	Using a maltose-binding-protein-APP fusion protein and human very-low-density lipoprotein (VLDL), we detected an interaction of apoE with APP that was inhibited by Abeta or anti-apoE antibody.	Maltose	8-15	apolipoprotein E	Homo sapiens	128-132
9224643-3	1997	Using a maltose-binding-protein-APP fusion protein and human very-low-density lipoprotein (VLDL), we detected an interaction of apoE with APP that was inhibited by Abeta or anti-apoE antibody.	Maltose	8-15	apolipoprotein E	Homo sapiens	178-182
9247703-10	1997	rGal was highly specific for alpha-D-galactosyl residues and degraded B oligosaccharide.	Maltose	29-36	galanin and GMAP prepropeptide	Rattus norvegicus	0-4
9225058-2	1997	In vitro, a fusion protein of BBTV Rep linked to a maltose-binding protein exhibited both site-specific nicking and joining activities.	Maltose	51-58	replication initiation protein	Banana bunchy top virus	35-38
9214624-3	1997	We mutagenized the EAA regions of MalF and MalG proteins of the Escherichia coli maltose transport system.	Maltose	81-88	Eaa protein	Escherichia coli	19-22
9037707-5	1997	The conformation of the recombinant protein, excluding the inserted segment, closely resembles that of wild-type MBP in the closed maltose-bound form.	Maltose	131-138	myelin basic protein	Homo sapiens	113-116
9210174-0	1997	Endogenous CCK in the control of gastric emptying of glucose and maltose.	Maltose	65-72	cholecystokinin	Macaca mulatta	11-14
9210174-1	1997	A role for endogenous cholecystokinin (CCK) in the control of gastric emptying of liquid glucose and maltose test meals in rhesus monkeys was assessed.	Maltose	101-108	cholecystokinin	Macaca mulatta	22-37
9210174-1	1997	A role for endogenous cholecystokinin (CCK) in the control of gastric emptying of liquid glucose and maltose test meals in rhesus monkeys was assessed.	Maltose	101-108	cholecystokinin	Macaca mulatta	39-42
8809039-4	1996	The CRD of SP-D, without the neck region peptide, was also expressed and shown to behave as a monomer that showed a very weak affinity for maltose-agarose, LPSs and phospholipids.	Maltose	139-146	surfactant protein D	Homo sapiens	11-15
8953715-0	1996	Alleviation of glucose repression of maltose metabolism by MIG1 disruption in Saccharomyces cerevisiae.	Maltose	37-44	transcription factor MIG1	Saccharomyces cerevisiae S288C	59-63
8953715-3	1996	In the MIG1-disrupted haploid strain, glucose repression was partly alleviated; i.e., maltose metabolism was initiated at higher glucose concentrations than in the corresponding wild-type strain.	Maltose	86-93	transcription factor MIG1	Saccharomyces cerevisiae S288C	7-11
8953715-4	1996	In contrast, the polyploid delta mig1 strain exhibited an even more stringent glucose control of maltose metabolism than the corresponding wild-type strain, which could be explained by a more rigid catabolite inactivation of maltose permease, affecting the uptake of maltose.	Maltose	97-104	transcription factor MIG1	Saccharomyces cerevisiae S288C	33-37
8953715-4	1996	In contrast, the polyploid delta mig1 strain exhibited an even more stringent glucose control of maltose metabolism than the corresponding wild-type strain, which could be explained by a more rigid catabolite inactivation of maltose permease, affecting the uptake of maltose.	Maltose	225-232	transcription factor MIG1	Saccharomyces cerevisiae S288C	33-37
8909283-5	1996	The corresponding proteins hCRY1 and hCRY2 were purified and characterized as maltose-binding fusion proteins.	Maltose	78-85	cryptochrome circadian regulator 1	Homo sapiens	27-32
8909283-5	1996	The corresponding proteins hCRY1 and hCRY2 were purified and characterized as maltose-binding fusion proteins.	Maltose	78-85	cryptochrome circadian regulator 2	Homo sapiens	37-42
8573072-8	1996	When the target sequence of the restriction protease factor Xa (Ile-Glu-Gly-Arg) was used as the linker between maltose-binding protein and human phenylalanine hydroxylase, cleavage of the fusion protein gave a mixture of full-length hydroxylase and a truncated form of the enzyme lacking the 13 N-terminal residues.	Maltose	112-119	coagulation factor X	Homo sapiens	53-62
8663400-7	1996	This mutant MBP confers a dominant-negative phenotype for growth on maltose, for maltose transport, and for maltose chemotaxis.	Maltose	68-75	myelin basic protein	Homo sapiens	12-15
8663400-7	1996	This mutant MBP confers a dominant-negative phenotype for growth on maltose, for maltose transport, and for maltose chemotaxis.	Maltose	81-88	myelin basic protein	Homo sapiens	12-15
8663400-7	1996	This mutant MBP confers a dominant-negative phenotype for growth on maltose, for maltose transport, and for maltose chemotaxis.	Maltose	81-88	myelin basic protein	Homo sapiens	12-15
8728991-5	1996	To test its antigenicity a recombinant Hsp70 protein fused to the maltose-binding protein was produced in Escherichia coli using the expression vector pMAL-cRI.	Maltose	66-73	heat shock protein 1B	Mus musculus	39-44
8812848-5	1996	Fusion apo(a) Kr V was isolated from cytoplasmic extracts and purified by amylose-agarose affinity chromatography by eluting with 10 mM maltose.	Maltose	136-143	lipoprotein(a)	Homo sapiens	7-13
8865073-5	1996	Intraduodenal administration of maltose (300 mM), hypertonic saline (500 mosmol l-1) and mucosal light stroking in anaesthetized rats evoked 70, 57 and 200% increases, respectively, in pancreatic protein secretion with no changes in plasma CCK concentration.	Maltose	32-39	cholecystokinin	Rattus norvegicus	240-243
8865073-10	1996	Infusion of a subthreshold dose of the octapeptide of CCK (15 pmol (kg body wt)-1 h-1) potentiated the pancreatic response to duodenal infusion of maltose (300 mM) and hypertonic saline (500 mosmol l-1).	Maltose	147-154	cholecystokinin	Rattus norvegicus	54-57
8878037-5	1996	Concomitantly, transcription initiation of the maltose-utilization operon malRA, including the alpha-glucosidase gene malA, was no longer subject to glucose-specific control.	Maltose	47-54	alpha-glucosidase	Staphylococcus xylosus	95-112
8735086-4	1996	The fusion polypeptide MBP-LLO411 was purified by maltose affinity chromatography and was further evaluated as a diagnostic antigen in a Western blot assay.	Maltose	50-57	myelin basic protein	Homo sapiens	23-26
8790294-6	1996	The function of atJ1 was tested by complementation of a dnaJ deletion mutant of E. coli, allowing growth in minimal medium at 44 degrees C. The AtJ1 protein was expressed in E. coli as a fusion with the maltose binding protein.	Maltose	203-210	DNAJ heat shock family protein	Arabidopsis thaliana	16-20
8790294-6	1996	The function of atJ1 was tested by complementation of a dnaJ deletion mutant of E. coli, allowing growth in minimal medium at 44 degrees C. The AtJ1 protein was expressed in E. coli as a fusion with the maltose binding protein.	Maltose	203-210	DNAJ heat shock family protein	Arabidopsis thaliana	144-148
8573072-8	1996	When the target sequence of the restriction protease factor Xa (Ile-Glu-Gly-Arg) was used as the linker between maltose-binding protein and human phenylalanine hydroxylase, cleavage of the fusion protein gave a mixture of full-length hydroxylase and a truncated form of the enzyme lacking the 13 N-terminal residues.	Maltose	112-119	phenylalanine hydroxylase	Homo sapiens	146-171
8594329-5	1995	Like Mal61p, Agt1p is a high-affinity, maltose/proton symporter, but Mal61p is capable of transporting only maltose and turanose, while Agt1p transports these two alpha-glucosides as well as several others including isomaltose, alpha-methylglucoside, maltotriose, palatinose, trehalose and melezitose.	Maltose	39-46	alpha-glucoside permease	Saccharomyces cerevisiae S288C	13-18
8530488-7	1995	A recombinant protein consisting of the GAP-related domain of p98 fused to maltose-binding protein stimulated GTPase activity of R-Ras, and showed a weak effect on that of Ha-Ras but not that of Rap1 or Rho.	Maltose	75-82	RAS related	Bos taurus	129-134
7499256-1	1995	The carboxyl-terminal domain (BC domain, roughly 100 amino acid residues) of the cytokine receptor homologous region in the receptor for murine granulocyte colony-stimulating factor was secreted as a maltose binding protein fusion into the Escherichia coli periplasm.	Maltose	200-207	colony stimulating factor 3 (granulocyte)	Mus musculus	144-181
7559400-1	1995	Rat T lymphocyte alloantigen 6.1 (RT6.1), which was synthesized as the fusion protein with a maltose-binding protein in Escherichia coli, displayed NAD(+)-dependent auto-ADP-ribosylation in addition to an enzyme activity of NAD+ glycohydrolase.	Maltose	93-100	ADP-ribosyltransferase 2b	Rattus norvegicus	34-39
8594329-5	1995	Like Mal61p, Agt1p is a high-affinity, maltose/proton symporter, but Mal61p is capable of transporting only maltose and turanose, while Agt1p transports these two alpha-glucosides as well as several others including isomaltose, alpha-methylglucoside, maltotriose, palatinose, trehalose and melezitose.	Maltose	108-115	alpha-glucoside permease	Saccharomyces cerevisiae S288C	13-18
8594329-6	1995	AGT1 expression is maltose inducible and induction is mediated by the Mal-activator.	Maltose	19-26	alpha-glucoside permease	Saccharomyces cerevisiae S288C	0-4
8594329-7	1995	The sequence of the upstream region of AGT1 is identical to that of the maltose-inducible MAL61 gene over a 469 bp region containing the UASMAL but the 315 bp sequence immediately upstream of AGT1 shows no significant homology to the sequence immediately upstream of MAL61.	Maltose	72-79	alpha-glucoside permease	Saccharomyces cerevisiae S288C	39-43
7642141-6	1995	The carbon source-dependent expression was further investigated by the use of an ACS1::lacZ fusion gene, showing complete repression on easily fermentable sugars such as glucose, maltose, sucrose or galactose.	Maltose	179-186	acetate--CoA ligase 1	Saccharomyces cerevisiae S288C	81-85
7496532-7	1995	Moreover, evidence is provided that the IMP2 gene product regulates galactose- and maltose-inducible genes at the transcriptional level and is a positive regulator of maltase, maltose permease and galactose permease gene expression.	Maltose	83-90	endopeptidase catalytic subunit	Saccharomyces cerevisiae S288C	40-44
7626234-1	1995	The hydrolysis of maltose and isomaltose and of sucrose and isomaltose at two different catalytic sites of sucrase-isomaltase has been demonstrated.	Maltose	18-25	sucrase-isomaltase	Homo sapiens	107-125
7651347-1	1995	In Enterobacteriaceae the nonphosphorylated form of IIAGlc of the phosphoenolpyruvate-dependent phosphotransferase system (PTS) can inhibit the uptake and subsequent metabolism of glycerol and maltose by binding to, and inhibiting, glycerol kinase and the MalK protein of the maltose transport system, respectively.	Maltose	193-200	ABC transporter ATP-binding protein	Salmonella enterica subsp. enterica serovar Typhimurium str. LT2	256-260
7651347-1	1995	In Enterobacteriaceae the nonphosphorylated form of IIAGlc of the phosphoenolpyruvate-dependent phosphotransferase system (PTS) can inhibit the uptake and subsequent metabolism of glycerol and maltose by binding to, and inhibiting, glycerol kinase and the MalK protein of the maltose transport system, respectively.	Maltose	276-283	ABC transporter ATP-binding protein	Salmonella enterica subsp. enterica serovar Typhimurium str. LT2	256-260
7782337-9	1995	Carbohydrates competed for SP-D binding to PI such that maltose > galactose for rSP-D, and the order was reversed for SP-DE321Q,N323D.	Maltose	56-63	surfactant protein D	Rattus norvegicus	27-31
7782337-9	1995	Carbohydrates competed for SP-D binding to PI such that maltose > galactose for rSP-D, and the order was reversed for SP-DE321Q,N323D.	Maltose	56-63	surfactant protein D	Rattus norvegicus	83-88
7543294-3	1995	Northwestern blotting experiments showed that a maltose-binding protein-Tenr fusion binds to a variety of RNAs in vitro and that it does not bind to single-stranded or double-stranded DNA.	Maltose	48-55	adenosine deaminase domain containing 1 (testis specific)	Mus musculus	72-76
7695920-8	1995	Migration toward SP-D was markedly inhibited (< 10% of controls) by 10 mM maltose but was not significantly inhibited by to 50 mM lactose.	Maltose	77-84	surfactant protein D	Homo sapiens	17-21
7758883-3	1995	ICA69 antibodies were determined by Western blot using an affinity purified recombinant fusion protein of ICA69 and maltose binding protein.	Maltose	116-123	islet cell autoantigen 1	Homo sapiens	0-5
7891724-8	1995	Addition of maltose-binding protein-AH/PH fusion recombinant protein, which is expected to bind Akt, to the immunoprecipitates from serum-starved cells induced the activation of the Akt kinase.	Maltose	12-19	thymoma viral proto-oncogene 1	Mus musculus	96-99
7891724-8	1995	Addition of maltose-binding protein-AH/PH fusion recombinant protein, which is expected to bind Akt, to the immunoprecipitates from serum-starved cells induced the activation of the Akt kinase.	Maltose	12-19	thymoma viral proto-oncogene 1	Mus musculus	182-185
7570631-5	1995	Genes coding for three proteins, dendrotoxins (DTX) K, I, and E, were expressed as maltose-binding (MBP) fusion proteins in the periplasmic space of Escherichia coli.	Maltose	83-90	myelin basic protein	Bos taurus	100-103
7890663-3	1995	ApoA-I was expressed in Escherichia coli as a fusion protein with the maltose binding protein, which was removed by factor Xa cleavage.	Maltose	70-77	apolipoprotein A-I	Oryctolagus cuniculus	0-6
7873598-6	1995	These activities were inhibited by D-mannose, N-acetyl-D-galactosamine, and D-maltose which are haptenic saccharides of authentic hemocytin.	Maltose	76-85	hemocytin	Bombyx mori	130-139
7857302-1	1995	The ligand-binding domain of human retinoic acid receptor alpha (hRAR alpha) was photoaffinity-labeled with a fluorescent retinoid, ADAM-3, by the use of a recombinant fused protein constructed from a maltose-binding protein and the E/F-domain of hRAR alpha (MBP-RAR alpha/E), which was expressed in E. coli.	Maltose	201-208	retinoic acid receptor alpha	Homo sapiens	35-63
7857302-1	1995	The ligand-binding domain of human retinoic acid receptor alpha (hRAR alpha) was photoaffinity-labeled with a fluorescent retinoid, ADAM-3, by the use of a recombinant fused protein constructed from a maltose-binding protein and the E/F-domain of hRAR alpha (MBP-RAR alpha/E), which was expressed in E. coli.	Maltose	201-208	retinoic acid receptor alpha	Homo sapiens	65-75
7857302-1	1995	The ligand-binding domain of human retinoic acid receptor alpha (hRAR alpha) was photoaffinity-labeled with a fluorescent retinoid, ADAM-3, by the use of a recombinant fused protein constructed from a maltose-binding protein and the E/F-domain of hRAR alpha (MBP-RAR alpha/E), which was expressed in E. coli.	Maltose	201-208	ADAM metallopeptidase domain 3A (pseudogene)	Homo sapiens	132-138
7857302-1	1995	The ligand-binding domain of human retinoic acid receptor alpha (hRAR alpha) was photoaffinity-labeled with a fluorescent retinoid, ADAM-3, by the use of a recombinant fused protein constructed from a maltose-binding protein and the E/F-domain of hRAR alpha (MBP-RAR alpha/E), which was expressed in E. coli.	Maltose	201-208	retinoic acid receptor alpha	Homo sapiens	66-75
7824276-3	1995	Direct binding of copper to p53 in the form of Cu(I) was demonstrated by Electron Spin Resonance using a purified recombinant protein containing residues 1-343 of murine wild-type p53 fused to E. coli maltose binding protein.	Maltose	201-208	transformation related protein 53, pseudogene	Mus musculus	28-31
9634779-5	1995	Moreover, the interaction between calmodulin and peptide ligands could provide a means of heterodimerization of proteins, as illustrated by the assembly of an antibody-calmodulin fusion with maltose binding protein tagged with a peptide ligand of calmodulin.	Maltose	191-198	calmodulin 1	Homo sapiens	34-44
9634779-5	1995	Moreover, the interaction between calmodulin and peptide ligands could provide a means of heterodimerization of proteins, as illustrated by the assembly of an antibody-calmodulin fusion with maltose binding protein tagged with a peptide ligand of calmodulin.	Maltose	191-198	calmodulin 1	Homo sapiens	168-178
9634779-5	1995	Moreover, the interaction between calmodulin and peptide ligands could provide a means of heterodimerization of proteins, as illustrated by the assembly of an antibody-calmodulin fusion with maltose binding protein tagged with a peptide ligand of calmodulin.	Maltose	191-198	calmodulin 1	Homo sapiens	168-178
7988695-0	1994	Accumulation of trehalose in Saccharomyces cerevisiae growing on maltose is dependent on the TPS1 gene encoding the UDPglucose-linked trehalose synthase.	Maltose	65-72	alpha,alpha-trehalose-phosphate synthase (UDP-forming) TPS1	Saccharomyces cerevisiae S288C	93-97
7966602-5	1994	We report that (i) a polyclonal rabbit antiserum generated against a chimeric protein consisting of the bacterial maltose-binding protein fused in frame to the majority of sequences contained in the second exon of the UL15 gene reacted with two proteins with M(r) of 35,000 and 75,000, respectively, in cells infected with a virus containing the authentic gene yielding a spliced mRNA or with a virus in which the authentic UL15 gene was replaced with a cDNA copy.	Maltose	114-121	DNA packaging terminase subunit 1	Human alphaherpesvirus 1	218-222
7966602-5	1994	We report that (i) a polyclonal rabbit antiserum generated against a chimeric protein consisting of the bacterial maltose-binding protein fused in frame to the majority of sequences contained in the second exon of the UL15 gene reacted with two proteins with M(r) of 35,000 and 75,000, respectively, in cells infected with a virus containing the authentic gene yielding a spliced mRNA or with a virus in which the authentic UL15 gene was replaced with a cDNA copy.	Maltose	114-121	DNA packaging terminase subunit 1	Human alphaherpesvirus 1	424-428
7802263-2	1994	The mutant MBP has an approximately 2-fold lower affinity for maltose, and the cysteine residue can be modified with 4-[N-(2-(iodoacetoxy)ethyl)-N-methylamino]-7-nitrobenz-2-oxa-1,3-diazole (IANBD) and 6-acryloyl-2-(dimethylamino)-naphthalene (acrylodan).	Maltose	62-69	myelin basic protein	Homo sapiens	11-14
7870126-6	1994	The lambda TcA2 cDNA insert was subcloned into the plasmid pPR987 which generated a 47-kDa maltose-binding fusion protein (TcA2-MBP).	Maltose	91-98	myelin basic protein	Bos taurus	128-131
16349415-1	1994	A color variant strain of Aureobasidium pullulans (NRRL Y-12974) produced beta-glucosidase activity when grown in liquid culture on a variety of carbon sources, such as cellobiose, xylose, arabinose, lactose, sucrose, maltose, glucose, xylitol, xylan, cellulose, starch, and pullulan.	Maltose	218-225	beta-glucosidase	Zea mays	74-90
7531538-5	1994	An IGFBP-4/maltose binding protein fusion peptide expression in the pMal-p2 vector produced a fusion protein exhibiting both IGFBP immunoreactivity and IGF-I binding activity with specificity characteristic of IGFBPs.	Maltose	11-18	insulin-like growth factor binding protein 4	Mus musculus	3-10
7765772-0	1994	Overproduction and purification of Lon protease from Escherichia coli using a maltose-binding protein fusion system.	Maltose	78-85	putative ATP-dependent Lon protease	Escherichia coli	35-38
7531538-5	1994	An IGFBP-4/maltose binding protein fusion peptide expression in the pMal-p2 vector produced a fusion protein exhibiting both IGFBP immunoreactivity and IGF-I binding activity with specificity characteristic of IGFBPs.	Maltose	11-18	insulin-like growth factor 1	Mus musculus	152-157
7531538-5	1994	An IGFBP-4/maltose binding protein fusion peptide expression in the pMal-p2 vector produced a fusion protein exhibiting both IGFBP immunoreactivity and IGF-I binding activity with specificity characteristic of IGFBPs.	Maltose	11-18	insulin like growth factor binding protein 4	Homo sapiens	210-216
7520915-1	1994	The amino-terminal domain of the cytokine receptor homologous region (BN domain; roughly 100 amino acid residues) in the receptor for murine granulocyte colony-stimulating factor (G-CSF) was secreted as a maltose-binding protein fusion into the Escherichia coli periplasm.	Maltose	205-212	colony stimulating factor 3 (granulocyte)	Mus musculus	141-178
7520915-1	1994	The amino-terminal domain of the cytokine receptor homologous region (BN domain; roughly 100 amino acid residues) in the receptor for murine granulocyte colony-stimulating factor (G-CSF) was secreted as a maltose-binding protein fusion into the Escherichia coli periplasm.	Maltose	205-212	colony stimulating factor 3 (granulocyte)	Mus musculus	180-185
7990831-2	1994	It is important that the N-terminal region of recombinant TP1 was represented by a maltose-binding protein.	Maltose	83-90	transition protein 1	Homo sapiens	58-61
8011639-6	1994	We have expressed a corresponding segment of the human Raf sequence (Raf55-132) in Escherichia coli as a fusion with maltose binding protein.	Maltose	117-124	zinc fingers and homeoboxes 2	Homo sapiens	55-58
7920705-3	1994	Yeast cells transformed with vectors allowing expression of either SUC1 or SUC2 under the control of the promoter of the yeast plasma membrane ATPase gene (PMA1) transport sucrose, and to a lesser extent also maltose, across their plasma membranes in an energy-dependent manner.	Maltose	209-216	sucrose-proton symporter 1	Arabidopsis thaliana	67-71
7920705-3	1994	Yeast cells transformed with vectors allowing expression of either SUC1 or SUC2 under the control of the promoter of the yeast plasma membrane ATPase gene (PMA1) transport sucrose, and to a lesser extent also maltose, across their plasma membranes in an energy-dependent manner.	Maltose	209-216	beta-fructofuranosidase SUC2	Saccharomyces cerevisiae S288C	75-79
7920705-3	1994	Yeast cells transformed with vectors allowing expression of either SUC1 or SUC2 under the control of the promoter of the yeast plasma membrane ATPase gene (PMA1) transport sucrose, and to a lesser extent also maltose, across their plasma membranes in an energy-dependent manner.	Maltose	209-216	H(+)-exporting P2-type ATPase PMA1	Saccharomyces cerevisiae S288C	156-160
7765034-3	1994	An extract of E. coli JM109 harboring pBETA92 had beta-amylase activity that produced beta-maltose from soluble starch.	Maltose	86-98	1,4-alpha-D-glucan maltohydrolase	Hordeum vulgare	50-62
8190127-4	1994	A bacterially expressed maltose binding protein-Lyn (MBP-Lyn) fusion protein was already tyrosine phosphorylated and had tyrosine kinase activity.	Maltose	24-31	LYN proto-oncogene, Src family tyrosine kinase	Rattus norvegicus	48-51
8190127-4	1994	A bacterially expressed maltose binding protein-Lyn (MBP-Lyn) fusion protein was already tyrosine phosphorylated and had tyrosine kinase activity.	Maltose	24-31	myelin basic protein	Rattus norvegicus	53-56
8190127-4	1994	A bacterially expressed maltose binding protein-Lyn (MBP-Lyn) fusion protein was already tyrosine phosphorylated and had tyrosine kinase activity.	Maltose	24-31	LYN proto-oncogene, Src family tyrosine kinase	Rattus norvegicus	57-60
8288553-1	1994	In enteric bacteria, chromosomally encoded permeases specific for lactose, maltose, and melibiose are allosterically regulated by the glucose-specific enzyme IIA of the phosphotransferase system.	Maltose	75-82	colicin Ia immunity protein	Escherichia coli	158-161
8112601-6	1994	As a basis for further investigations concerning the structure-function relationship and to generate a source of recombinant protein for X-ray crystallography studies, LCN1 was produced in Escherichia coli as a fusion with maltose-binding protein.	Maltose	223-230	lipocalin 1	Homo sapiens	168-172
8221926-6	1993	Furthermore TYE2 function seems to be important for the expression of a variety of Ty-unrelated functions such as ADH1 expression, sporulation, growth on maltose, galactose, raffinose, and on non-fermentable carbon sources.	Maltose	154-161	Swi3p	Saccharomyces cerevisiae S288C	12-16
8224161-2	1993	Recombinant malE-mos protein (Xenopus mos protooncogene fused in frame to the maltose binding protein of E. coli) activates MAP kinase in cell-free extracts prepared from Xenopus oocytes and eggs.	Maltose	78-85	MOS proto-oncogene, serine/threonine kinase L homeolog	Xenopus laevis	17-20
8224161-2	1993	Recombinant malE-mos protein (Xenopus mos protooncogene fused in frame to the maltose binding protein of E. coli) activates MAP kinase in cell-free extracts prepared from Xenopus oocytes and eggs.	Maltose	78-85	MOS proto-oncogene, serine/threonine kinase L homeolog	Xenopus laevis	38-41
8215379-2	1993	The energy requirement for maltose transport was evaluated with a metabolic model based on an experimental value of YATP for growth on glucose and an ATP requirement for maltose transport of 1 mol.mol-1.	Maltose	27-34	thiamine thiazole synthase	Saccharomyces cerevisiae S288C	197-202
8457197-4	1993	Moreover, D-glucose and maltose competitively inhibit fructose transport by GLUT2 and galactose transport by GLUT3, indicating that the transport of the alternative substrates for these transporters is likely to be mediated by the same outward-facing sugar-binding site used by glucose.	Maltose	24-31	solute carrier family 2 member 2 S homeolog	Xenopus laevis	76-81
8352755-6	1993	The order of inhibiting potency on the binding of SP-A was: N-acetylmannosamine > L-fucose, maltose > glucose > mannose.	Maltose	95-102	surfactant protein A2	Homo sapiens	50-54
8100774-12	1993	Here we show that the carboxy-terminal 192 amino acids of invasin expressed as a fusion protein with the maltose binding protein of E. coli is capable of delivering co-stimulatory signals to human T cells through the beta 1 integrins.	Maltose	105-112	integrin subunit beta 1	Homo sapiens	217-233
8501032-3	1993	The glucokinase-dependent strain accumulates substantial amounts of glucose internally in batch culture after exhaustion of glucose, as well as from maltose.	Maltose	149-156	glucokinase	Saccharomyces cerevisiae S288C	4-15
8486682-12	1993	An inhibition assay with biotinylated CL-43, using solid-phase mannan as ligand, revealed the following carbohydrate inhibition pattern: mannose and ManNAc > fucose > GlcNAc > glucose and maltose > galactose > lactose >> GalNAc.	Maltose	197-204	collectin-43	Bos taurus	38-43
8498606-6	1993	Previously we demonstrated that CCK receptor antagonists attenuate suppression of sham feeding by intestinal infusion of either oleate or maltose, suggesting that endogenous CCK participates in suppression of sham feeding by some intestinal nutrients.	Maltose	138-145	cholecystokinin	Rattus norvegicus	32-35
8498606-6	1993	Previously we demonstrated that CCK receptor antagonists attenuate suppression of sham feeding by intestinal infusion of either oleate or maltose, suggesting that endogenous CCK participates in suppression of sham feeding by some intestinal nutrients.	Maltose	138-145	cholecystokinin	Rattus norvegicus	174-177
8457197-4	1993	Moreover, D-glucose and maltose competitively inhibit fructose transport by GLUT2 and galactose transport by GLUT3, indicating that the transport of the alternative substrates for these transporters is likely to be mediated by the same outward-facing sugar-binding site used by glucose.	Maltose	24-31	solute carrier family 2 member 3 L homeolog	Xenopus laevis	109-114
1339284-1	1992	Human pulmonary surfactant protein D (SP-D) was identified in lung lavage by its similarity to rat SP-D in both its molecular mass and its Ca(2+)-dependent-binding affinity for maltose [Persson, Chang & Crouch (1990) J. Biol.	Maltose	177-184	surfactant protein D	Rattus norvegicus	6-36
8425548-0	1993	Homology of pyridoxal-5"-phosphate-dependent aminotransferases with the cobC (cobalamin synthesis), nifS (nitrogen fixation), pabC (p-aminobenzoate synthesis) and malY (abolishing endogenous induction of the maltose system) gene products.	Maltose	208-215	NFS1 cysteine desulfurase	Homo sapiens	100-104
8425548-1	1993	Bacterial deletion mutants have indicated that the gene products of cobC, nifS, pabC and malY participate in important metabolic pathways, i.e. cobalamin synthesis, nitrogen fixation, synthesis of p-aminobenzoate and the regulation of the maltose system, respectively.	Maltose	239-246	NFS1 cysteine desulfurase	Homo sapiens	74-78
1280430-1	1992	Putative E2/NS1 sequence of hepatitis C virus was expressed in E. coli as a fusion protein with maltose binding protein.	Maltose	96-103	influenza virus NS1A binding protein	Homo sapiens	12-15
1432639-3	1992	Values of the enthalpy and entropy of activation of the hydrolyses were positive and in the range reported for maltose, a result indicating that the hydrolyses proceeded according to the A-1 mechanism (i.e., unimolecular decomposition).	Maltose	111-118	immunoglobulin kappa variable 2D-30	Homo sapiens	187-190
1324436-4	1992	Here we predict the binding site of MBP to its receptor using a "binary docking" technique in which two MBP octapeptide sequences containing mutations that eliminate maltose chemotaxis are independently docked to the receptor.	Maltose	166-173	myelin basic protein	Homo sapiens	36-39
1324436-4	1992	Here we predict the binding site of MBP to its receptor using a "binary docking" technique in which two MBP octapeptide sequences containing mutations that eliminate maltose chemotaxis are independently docked to the receptor.	Maltose	166-173	myelin basic protein	Homo sapiens	104-107
1420600-0	1992	The immunomodulatory role of IFN-alpha or maltose-stabilized IFN-alpha on T-cell activation.	Maltose	42-49	interferon alpha 1	Homo sapiens	61-70
1420600-1	1992	The effects of human interferon-alpha (IFN-alpha) or maltose-stabilized IFN-alpha (MS-IFN-alpha) on IL-2 production by PHA- or anti-CD3 mAb-stimulated MOLT 16 cells, a human leukemic T cell line, were studied.	Maltose	53-60	interleukin 2	Homo sapiens	100-104
1420600-2	1992	MS-IFN-alpha is an IFN-alpha-containing powder in which maltose was used as an excipient, and has been shown to have a positive effect on human immunodeficiency virus (HIV)-infected patients.	Maltose	56-63	interferon alpha 1	Homo sapiens	3-12
1420600-2	1992	MS-IFN-alpha is an IFN-alpha-containing powder in which maltose was used as an excipient, and has been shown to have a positive effect on human immunodeficiency virus (HIV)-infected patients.	Maltose	56-63	interferon alpha 1	Homo sapiens	19-28
1436639-4	1992	Pretreatment with the specific CCK "A" receptor antagonist, MK329, completely abolished the effects of maltose on gastric emptying.	Maltose	103-110	cholecystokinin A receptor	Rattus norvegicus	31-47
1294292-0	1992	Strong competitive inhibition of porcine pancreatic alpha-amylase by aminodeoxy derivatives of maltose and maltotriose.	Maltose	95-102	amylase alpha 2A	Homo sapiens	41-65
1279986-3	1992	cDNA encoding the COOH-terminal 41 amino acids of NHE-1 was subcloned into a maltose-binding protein vector and the purified fusion protein (FP347A) used to immunize guinea pigs.	Maltose	77-84	sodium/hydrogen exchanger 1	Oryctolagus cuniculus	50-55
1343843-1	1992	Mixtures of maltose palmitates containing predominantly maltose tetrapalmitate (designated MTP) possess immune potentiating and antitumor properties.	Maltose	12-19	metallothionein 1B	Homo sapiens	91-94
1339284-1	1992	Human pulmonary surfactant protein D (SP-D) was identified in lung lavage by its similarity to rat SP-D in both its molecular mass and its Ca(2+)-dependent-binding affinity for maltose [Persson, Chang & Crouch (1990) J. Biol.	Maltose	177-184	surfactant protein D	Rattus norvegicus	38-42
1339284-1	1992	Human pulmonary surfactant protein D (SP-D) was identified in lung lavage by its similarity to rat SP-D in both its molecular mass and its Ca(2+)-dependent-binding affinity for maltose [Persson, Chang & Crouch (1990) J. Biol.	Maltose	177-184	surfactant protein D	Rattus norvegicus	99-103
1339284-4	1992	For structural studies, human SP-D was isolated from amniotic fluid by affinity chromatography on maltose-Sepharose followed by f.p.l.c.	Maltose	98-105	surfactant protein D	Homo sapiens	30-34
1521938-6	1992	The results showed that both lectin- and PMA/ionomycin-induced mitogenesis and IL2-dependent proliferation of T-cells from ethanol diet-fed mice were diminished as compared with that of maltose-substitute diet or standard liquid diet.	Maltose	186-193	peroneal muscular atrophy	Mus musculus	29-44
1521938-6	1992	The results showed that both lectin- and PMA/ionomycin-induced mitogenesis and IL2-dependent proliferation of T-cells from ethanol diet-fed mice were diminished as compared with that of maltose-substitute diet or standard liquid diet.	Maltose	186-193	interleukin 2	Mus musculus	79-82
1373576-3	1992	Suppression of sham feeding by oleic acid or maltose was attenuated by CCK-receptor antagonists, while suppression of sham feeding by L-Phe was not.	Maltose	45-52	cholecystokinin	Homo sapiens	71-74
1373576-7	1992	These results suggest 1) that endogenous CCK mediates suppression of sham feeding by oleate and maltose but not by L-Phe and 2) that CCK participating in suppression of feeding by intestinal stimuli might not be of endocrine origin.	Maltose	96-103	cholecystokinin	Homo sapiens	41-44
1547886-2	1992	Titrations with maltose yield three isosbestic points in the difference spectrum of MBP, consistent with two protein conformations: ligand-free and ligand-bound.	Maltose	16-23	myelin basic protein	Homo sapiens	84-87
1729468-2	1992	Starch, a polysaccharide composed of alpha 1,4-linked glucose units (amylose) and alpha 1,4-1,6-linked branched structure (amylopectin), is cleaved in the duodenal cavity by secreted pancreatic alpha-amylase to a disaccharide (maltose), trisaccharide (maltotriose), and branched alpha-dextrins.	Maltose	227-234	amylase alpha 2A	Homo sapiens	183-207
1561839-0	1992	IMP2, a nuclear gene controlling the mitochondrial dependence of galactose, maltose and raffinose utilization in Saccharomyces cerevisiae.	Maltose	76-83	endopeptidase catalytic subunit	Saccharomyces cerevisiae S288C	0-4
1561839-1	1992	The IMP2 gene of Saccharomyces cerevisiae is involved in the nucleo-mitochondrial control of maltose, galactose and raffinose utilization as shown by the inability of imp2 mutants to grow on these carbon sources in respiratory-deficient conditions or in the presence of ethidium bromide and erythromycin.	Maltose	93-100	endopeptidase catalytic subunit	Saccharomyces cerevisiae S288C	4-8
1596914-0	1992	Photolabile derivatives of maltose and maltotriose as ligands for the affinity labelling of the maltodextrin-binding site in porcine pancreatic alpha-amylase.	Maltose	27-34	amylase alpha 2A	Homo sapiens	133-157
1874408-4	1991	They show over 50% similarity to the maltose transport proteins MalF and MalG and to the glycerol-3-phosphate uptake proteins UgpA and UgpE of Escherichia coli.	Maltose	37-44	SN-glycerol-3-phosphate transport system permease protein ugpA	Escherichia coli	126-130
24425332-2	1992	The specific activity of alpha-glucosidase depended on the dilution rate as well as the proportion of maltose in the mixture.	Maltose	102-109	sucrase-isomaltase	Homo sapiens	25-42
24425332-3	1992	The chemostat provides a way of reaching the low residual concentrations of glucose in the broth that are necessary to release catabolite repression and permit maltose induction of alpha-glucosidase.	Maltose	160-167	sucrase-isomaltase	Homo sapiens	181-198
1778982-1	1991	Porcine pancreatic alpha-amylase (1,4-alpha-D-glucan glucanohydrolase) [EC 3.2.1.1] has both amylase activity (hydrolysis of alpha-1,4-D-glucoside bond of starch) and maltosidase activity (hydrolysis of p-nitrophenyl-alpha-D-maltoside to p-nitrophenol and maltose).	Maltose	256-263	amylase alpha 2A	Homo sapiens	8-32
1889400-2	1991	The hex2 mutants have pleiotropic defects in the regulation of glucose-repressible enzymes, hexokinase PII synthesis and maltose uptake [Entian, K.-D. & Zimmermann, F.K.	Maltose	121-128	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	4-8
1999393-3	1991	The high-affinity maltose transporter is maltose inducible and is encoded by the MAL11 (and/or MAL61) gene of the MAL1 (and/or MAL6) locus.	Maltose	18-25	alpha-glucoside permease	Saccharomyces cerevisiae S288C	81-86
1999393-3	1991	The high-affinity maltose transporter is maltose inducible and is encoded by the MAL11 (and/or MAL61) gene of the MAL1 (and/or MAL6) locus.	Maltose	41-48	alpha-glucoside permease	Saccharomyces cerevisiae S288C	81-86
2192262-6	1990	When a DNA fragment containing these sites was placed upstream of a CYC1-lacZ gene, maltose induced beta-galactosidase.	Maltose	84-91	cytochrome c isoform 1	Saccharomyces cerevisiae S288C	68-72
1881871-1	1991	The leucine zipper of the yeast transcriptional factor GCN4 was grafted to the C-terminal amino acid of the maltose binding protein (MalE) by fusing the malE gene of Escherichia coli to a synthetic gene coding for the leucine zipper.	Maltose	108-115	amino acid starvation-responsive transcription factor GCN4	Saccharomyces cerevisiae S288C	55-59
1904815-4	1991	The fluorescent derivatives of glucose and all its straight chain, alpha 1-4 linked, oligomers from maltose to maltoheptaose were well resolved.	Maltose	100-107	adrenoceptor alpha 1D	Homo sapiens	67-76
2256108-4	1990	Acid alpha-glucosidase could hydrolyze maltose about 10 times faster than isomaltose, and maltotetraose about 5 times faster than tetrasaccharide isolated from urine.	Maltose	39-46	sucrase-isomaltase	Homo sapiens	5-22
2256108-5	1990	In leucocytes of the patient with late onset glycogenosis type II, acid alpha-glucosidase activities towards maltose, isomaltose, maltotetraose and tetrasaccharide isolated from urine showed 75.3%, 67.4%, 76.5% and 41.4% of normal control values, respectively.	Maltose	109-116	sucrase-isomaltase	Homo sapiens	72-89
2124143-1	1990	The periplasmic maltose binding protein (MBP) is required for the high affinity transport of maltose and maltodextrins and for chemotaxis towards these sugars.	Maltose	16-23	myelin basic protein	Homo sapiens	41-44
2199604-1	1990	In hex2 mutants of Saccharomyces cerevisiae, which are defective in glucose repression of several enzymes, growth is inhibited if maltose is present in the medium.	Maltose	130-137	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	3-7
2199604-2	1990	After adding [14C]maltose to cultures growing with ethanol, maltose metabolism was followed in both hex2 mutant and wild-type cells.	Maltose	18-25	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	100-104
2199604-2	1990	After adding [14C]maltose to cultures growing with ethanol, maltose metabolism was followed in both hex2 mutant and wild-type cells.	Maltose	60-67	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	100-104
2199604-5	1990	Pulse-chase experiments showed that 2 h after addition of maltose, hex2 cells hydrolysed maltose to glucose, which was partially excreted into the medium.	Maltose	58-65	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	67-71
2199604-5	1990	Pulse-chase experiments showed that 2 h after addition of maltose, hex2 cells hydrolysed maltose to glucose, which was partially excreted into the medium.	Maltose	89-96	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	67-71
2199604-6	1990	31P-NMR studies gave evidence that turnover of sugar phosphates was completely abolished in hex2 cells after 2 h incubation with maltose.	Maltose	129-136	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	92-96
2199604-8	1990	Although maltose is taken up by proton symport, the internal pH in the hex2 mutant did not change markedly during the 5 h after adding maltose.	Maltose	9-16	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	71-75
2108147-2	1990	SP-D can be selectively and efficiently eluted from isolated rat surfactant with glucose, maltose, and certain other saccharides.	Maltose	90-97	surfactant protein D	Rattus norvegicus	0-4
2108147-6	1990	The most efficient inhibitors of SP-D binding were alpha-glucosyl-containing saccharides (e.g. isomaltose, maltose, malotriose).	Maltose	98-105	surfactant protein D	Rattus norvegicus	33-37
2108147-7	1990	SP-D showed quantitative binding to maltosyl-agarose and was specifically eluted with maltose or EDTA.	Maltose	86-93	surfactant protein D	Rattus norvegicus	0-4
2137884-2	1990	Maltoporin is an integral membrane protein, which forms a channel in the E. coli outer membrane that specifically facilitates the diffusion of maltose and maltodextrins.	Maltose	143-150	maltoporin	Escherichia coli	0-10
3042166-3	1988	MTP1, maps near MAL1, and either encodes a permease which transports melezitose, alpha-methylglucoside, and maltose or regulates the activity of such a permease.	Maltose	108-115	solute carrier family 40 member 1	Homo sapiens	0-4
33233136-6	2020	In vitro inhibition was quantified using potato starch (for amylases) and maltose (for alpha-glucosidase) as substrates.	Maltose	74-81	neutral alpha-glucosidase AB-like	Solanum tuberosum	87-104
8535163-4	1995	A cDNA for mature EDN was obtained by PCR and inserted in pMAL-cRI downstream of the malE gene encoding maltose binding protein.	Maltose	104-111	ribonuclease A family member 2	Homo sapiens	18-21
7925377-5	1994	In contrast, expression of the maltose permease gene (MAL11) and maltose utilization is normal.	Maltose	31-38	alpha-glucoside permease	Saccharomyces cerevisiae S288C	54-59
34624776-6	2022	Those effects were not really evident with alpha-glucosidase, likely due to the small molecular size of maltose substrate.	Maltose	104-111	sucrase-isomaltase	Homo sapiens	43-60
34768798-6	2021	alpha-TC deficient plants increased their oligosaccharide levels and reduced maltose amount, while excessive accumulation of alpha-TC corresponded with enhanced amounts of maltose.	Maltose	77-84	centroradiali	Arabidopsis thaliana	0-8
34519602-4	2021	Among of which maltose modified NSp had the strongest anti-tumor effects than that of glucose and maltotriose.	Maltose	15-22	serine peptidase inhibitor Kazal type 5	Homo sapiens	32-35
34392609-8	2021	Under the condition of 37 C, pH 4.0, equimolar maltose and ascorbic acid sodium salt, 8.7+-0.4 g/L of AA-2G was synthesized by rAGL.	Maltose	47-54	amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase	Rattus norvegicus	127-131
35605982-6	2022	For further validation, we also prepared a maltose-binding protein-linked IgG1-Fc fragment (MBP-Fc).	Maltose	43-50	myelin basic protein	Homo sapiens	92-95
34623258-6	2021	These experiments reveal differences in heterogeneity in the apo and holo conformational states of MBP and produce accurate quantification of the distributions among apo and holo conformational states at subsaturating maltose concentrations.	Maltose	218-225	myelin basic protein	Homo sapiens	99-102
34620864-2	2021	Previously, we showed that ageing colonies of an E. coli mutant unable to produce cAMP when grown on maltose, accumulated mutations in the crp gene (encoding a global transcription factor) and in genes involved in pyrimidine metabolism such as cmk; combined mutations in both crp and cmk enabled fermentation of maltose (which usually requires cAMP-mediated Crp activation for catabolic pathway expression).	Maltose	101-108	catabolite gene activator protein	Escherichia coli	139-142
34620864-2	2021	Previously, we showed that ageing colonies of an E. coli mutant unable to produce cAMP when grown on maltose, accumulated mutations in the crp gene (encoding a global transcription factor) and in genes involved in pyrimidine metabolism such as cmk; combined mutations in both crp and cmk enabled fermentation of maltose (which usually requires cAMP-mediated Crp activation for catabolic pathway expression).	Maltose	101-108	catabolite gene activator protein	Escherichia coli	358-361
34620864-2	2021	Previously, we showed that ageing colonies of an E. coli mutant unable to produce cAMP when grown on maltose, accumulated mutations in the crp gene (encoding a global transcription factor) and in genes involved in pyrimidine metabolism such as cmk; combined mutations in both crp and cmk enabled fermentation of maltose (which usually requires cAMP-mediated Crp activation for catabolic pathway expression).	Maltose	312-319	catabolite gene activator protein	Escherichia coli	358-361
34490352-10	2021	In this vein, we present a means to combine codon harmonization and a maltose-binding protein fusion tag to produce CCR3 from E. coli.	Maltose	70-77	C-C motif chemokine receptor 3	Homo sapiens	116-120
34140941-0	2021	Role of Elm1, Tos3, and Sak1 Protein Kinases in the Maltose Metabolism of Baker"s Yeast.	Maltose	52-59	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	8-12
34140941-0	2021	Role of Elm1, Tos3, and Sak1 Protein Kinases in the Maltose Metabolism of Baker"s Yeast.	Maltose	52-59	serine/threonine protein kinase SAK1	Saccharomyces cerevisiae S288C	24-28
34140941-3	2021	In this study, the focus was on the role of three kinases, Elm1, Tos3, and Sak1, in the maltose metabolism of baker"s yeast in lean dough.	Maltose	88-95	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	59-63
34140941-3	2021	In this study, the focus was on the role of three kinases, Elm1, Tos3, and Sak1, in the maltose metabolism of baker"s yeast in lean dough.	Maltose	88-95	serine/threonine protein kinase SAK1	Saccharomyces cerevisiae S288C	75-79
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	27-34	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	0-4
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	27-34	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	121-125
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	66-73	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	0-4
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	78-85	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	0-4
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	78-85	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	121-125
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	144-151	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	0-4
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	144-151	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	121-125
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	262-269	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	0-4
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	262-269	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	121-125
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	274-281	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	0-4
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	274-281	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	121-125
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	303-310	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	0-4
34140941-5	2021	Elm1 was necessary for the maltose metabolism of baker"s yeast in maltose and maltose-glucose, and the overexpression of ELM1 could enhance the maltose metabolism and lean dough fermentation ability by upregulating the transcription of MALx1 (x is the locus) in maltose and maltose-glucose and MALx2 in maltose.	Maltose	303-310	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	121-125
34140941-6	2021	The native level of TOS3 and SAK1 was essential for yeast cells to adapt glucose repression, but the overexpression of TOS3 and SAK1 alone repressed the expression of MALx1 in maltose-glucose and MALx2 in maltose.	Maltose	205-212	serine/threonine protein kinase SAK1	Saccharomyces cerevisiae S288C	128-132
34140941-8	2021	These results, for the first time, suggested that Elm1, rather than Tos3 and Sak1, might be the dominant regulator in the maltose metabolism of baker"s yeast.	Maltose	122-129	serine/threonine protein kinase ELM1	Saccharomyces cerevisiae S288C	50-54
34140941-8	2021	These results, for the first time, suggested that Elm1, rather than Tos3 and Sak1, might be the dominant regulator in the maltose metabolism of baker"s yeast.	Maltose	122-129	serine/threonine protein kinase SAK1	Saccharomyces cerevisiae S288C	77-81
34072539-6	2021	The biotinylated-IFN-gamma was incorporated with colloidal-gold-labeled 6HIS-maltose binding protein-monomeric streptavidin (6HISMBP-mSA) and absorbed at the conjugate pad.	Maltose	77-84	interferon gamma	Homo sapiens	17-26
34600402-4	2022	For this purpose, maltose binding protein harbouring the aD region (MBP-aD) was synthesized as a bioreceptor and immobilized on the screen-printed carbon electrode (SPCE).	Maltose	18-25	myelin basic protein	Homo sapiens	68-71
35473854-4	2022	In the first step, maltose is produced by catalyzing the hydrolysis of starch using sAA in the reaction chamber.	Maltose	19-26	serum amyloid A1 cluster	Homo sapiens	84-87
35448589-3	2022	In this study, we applied an evolutionary engineering strategy to alter the substrate specificity of the proton-coupled disaccharide transporter Mal11 in Saccharomyces cerevisiae, which has affinity for sucrose, maltose and glucose.	Maltose	212-219	alpha-glucoside permease	Saccharomyces cerevisiae S288C	145-150
35448589-4	2022	The introduction of MAL11 in a strain devoid of all other sugar transporters and disaccharide hydrolases restored growth on glucose but rendered the strain highly sensitive to the presence of sucrose or maltose.	Maltose	203-210	alpha-glucoside permease	Saccharomyces cerevisiae S288C	20-25
2531894-2	1989	When membrane vesicles were made from strains producing tethered maltose-binding proteins by dilution of spheroplasts into phosphate buffer, those from an F0F1 ATPase-containing (unc+) strain transported maltose in the presence of an exogenous electron donor, such as ascorbate/phenazine methosulfate, at a rate of 1-5 nmol/min per mg of protein, whereas those from an isogenic unc- strain failed to transport maltose.	Maltose	65-72	ATP synthase F1 subunit epsilon	Homo sapiens	155-166
2531894-2	1989	When membrane vesicles were made from strains producing tethered maltose-binding proteins by dilution of spheroplasts into phosphate buffer, those from an F0F1 ATPase-containing (unc+) strain transported maltose in the presence of an exogenous electron donor, such as ascorbate/phenazine methosulfate, at a rate of 1-5 nmol/min per mg of protein, whereas those from an isogenic unc- strain failed to transport maltose.	Maltose	204-211	ATP synthase F1 subunit epsilon	Homo sapiens	155-166
2531894-2	1989	When membrane vesicles were made from strains producing tethered maltose-binding proteins by dilution of spheroplasts into phosphate buffer, those from an F0F1 ATPase-containing (unc+) strain transported maltose in the presence of an exogenous electron donor, such as ascorbate/phenazine methosulfate, at a rate of 1-5 nmol/min per mg of protein, whereas those from an isogenic unc- strain failed to transport maltose.	Maltose	204-211	ATP synthase F1 subunit epsilon	Homo sapiens	155-166
2674122-8	1989	Furthermore, although TDG was shown to inhibit the uptake of maltose in the four parental strains, all of the mutant strains exhibited a dramatic resistance to TDG inhibition.	Maltose	61-68	thymine DNA glycosylase	Homo sapiens	22-25
2446870-1	1987	The primary structure of barley endosperm beta-amylase, an enzyme which catalyses the liberation of maltose from 1,4-alpha-D-glucans, has been deduced from the nucleotide sequence of a cloned full-length cDNA.	Maltose	100-107	1,4-alpha-D-glucan maltohydrolase	Hordeum vulgare	42-54
2460027-6	1988	Both alpha-glucosidase and amylase were produced at 20- to 40-fold-higher levels when B. vulgatus was grown on maltose, amylose, or amylopectin than when B. vulgatus was grown on glucose or other monosaccharides.	Maltose	111-118	sucrase-isomaltase	Homo sapiens	5-22
16347392-5	1987	The apparent K(m) values of alpha-amylase, pullulanase, and alpha-glucosidase for their corresponding substrates, starch, pullulan, and maltose were 0.35 mg/ml, 0.63 mg/ml, and 25 mM, respectively.	Maltose	136-143	sucrase-isomaltase	Homo sapiens	60-77
2971117-1	1988	Maltoporin (LamB protein), a protein of Escherichia coli outer membrane forms ionic channels with a selectivity for maltose and maltodextrins (Dargent et al., 1987).	Maltose	116-123	maltoporin	Escherichia coli	0-10
3302677-1	1987	The expression of the maltase (MALS) and the maltose permease (MALT) genes in Saccharomyces species is coregulated at the transcriptional level; they are coordinately induced by maltose in the presence of a positively acting regulatory (MALR) gene and carbon catabolite repressed by glucose.	Maltose	45-52	maltose permease	Saccharomyces cerevisiae S288C	63-67
4084861-6	1985	ruminicola GA33 (glucose), B. succinogenes S85 (cellobiose), and Succinivibrio dextrinosolvens 24 (maltose), it was 2 microgram X mL-1.	Maltose	99-106	L1 cell adhesion molecule	Mus musculus	130-134
3496119-10	1987	A method is proposed based on certain properties of porcine pancreatic alpha-amylase, especially the non-interaction of the p-nitrophenyl moiety of the maltose derivative with subsites 1 and 2, and the o-nitrophenyl group which interacts in a similar way to a glucose residue at the reducing end, and on the grounds that the amylase-amylose complexes are of the productive type.	Maltose	152-159	amylase alpha 2A	Homo sapiens	60-84
3035346-1	1987	The HEX2 gene which is necessary for glucose repression and is involved in the regulation of hexokinase PII synthesis and maltose uptake, has been cloned by complementation of a hex2 mutant, and selection for restored growth on maltose.	Maltose	122-129	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	4-8
3035346-1	1987	The HEX2 gene which is necessary for glucose repression and is involved in the regulation of hexokinase PII synthesis and maltose uptake, has been cloned by complementation of a hex2 mutant, and selection for restored growth on maltose.	Maltose	228-235	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	4-8
3035346-7	1987	Gene disruption of HEX2 yielded nonrepressible transformants with elevated hexokinase PII activity showing inhibition by maltose; this provides clear evidence that the HEX2 gene has been isolated.	Maltose	121-128	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	19-23
3035346-7	1987	Gene disruption of HEX2 yielded nonrepressible transformants with elevated hexokinase PII activity showing inhibition by maltose; this provides clear evidence that the HEX2 gene has been isolated.	Maltose	121-128	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	168-172
3525144-1	1986	The indolizidine alkaloid castanospermine (1,6,7,8-tetrahydroxyoctahydroindolizine) inhibits hydrolysis of maltose, glycogen and isomaltose by purified lysosomal alpha-glucosidase yielding Ki values of 0.095, 0.10 and 0.30 mumol/l, respectively.	Maltose	107-114	alpha glucosidase	Homo sapiens	152-179
2999779-5	1985	Production of cAMP in the transformant carrying CYR1 and either RAS2 or RAS2val19 was confirmed by staining colonies on maltose-MacConkey plates and by measuring induction of beta-galactosidase by isopropyl beta-D-thiogalactopyranoside.	Maltose	120-127	adenylate cyclase	Saccharomyces cerevisiae S288C	48-52
3891151-6	1985	Renal alpha-glucosidase has a higher affinity for maltose (Km, 0.8 mmol/l) than acid enzyme, however; for glycogen acid enzyme shows the highest affinity (20.7 g/l).	Maltose	50-57	sucrase-isomaltase	Homo sapiens	6-23
2582103-5	1985	Maltose, maltotriose and alpha-limit dextrins must diffuse across this first barrier to absorption to be hydrolyzed by maltase and sucrase-isomaltase immobilized at the membrane; however, the resultant glucose, once formed, accrues at the surface to provide a concentration advantage.	Maltose	0-7	8 sucrase-isomaltase (alpha-glucosidase)	Gallus gallus	131-149
3872211-0	1985	On porcine pancreatic alpha-amylase action: kinetic evidence for the binding of two maltooligosaccharide molecules (maltose, maltotriose and o-nitrophenylmaltoside) by inhibition studies.	Maltose	116-123	amylase alpha 2A	Homo sapiens	11-35
3872211-2	1985	Hydrolysis of small substrates (maltose, maltotriose and o-nitrophenylmaltoside) catalysed by porcine pancreatic alpha-amylase was studied from a kinetic viewpoint over a wide range of substrate concentrations.	Maltose	32-39	amylase alpha 2A	Homo sapiens	102-126
3872211-9	1985	These results are also consistent with the successive binding of at least two molecules of maltose or maltotriose per amylase molecule with the dissociation constants Ki1 and Ki2.	Maltose	91-98	TNF receptor superfamily member 8	Homo sapiens	167-170
2984252-8	1985	In the liver, but not in the kidney, diabetes and glucagon administration abolished the induction of aldolase B mRNAs in animals refed the maltose-rich diets.	Maltose	139-146	aldolase, fructose-bisphosphate B	Rattus norvegicus	101-111
3791296-2	1986	The reaction rate was greater with maltotriose than with maltose, and with increasing size of the cyclomalto-oligosaccharide (cG6 less than cG7 less than cG8).	Maltose	57-64	actin binding transcription modulator	Homo sapiens	154-157
3099348-4	1986	Native alpha-amylase had an activity of 2,730 mg maltose/min X mg enzyme and a Km of 0.222% amylose, the activity of calcium depleted amylase being of 1,640 mg maltose/min X mg enzyme and Km 0.571% amylose.	Maltose	49-56	LOW QUALITY PROTEIN: pancreatic alpha-amylase	Sus scrofa	7-20
3099348-4	1986	Native alpha-amylase had an activity of 2,730 mg maltose/min X mg enzyme and a Km of 0.222% amylose, the activity of calcium depleted amylase being of 1,640 mg maltose/min X mg enzyme and Km 0.571% amylose.	Maltose	160-167	LOW QUALITY PROTEIN: pancreatic alpha-amylase	Sus scrofa	7-20
3746458-9	1986	Glucose 6-phosphatase activity was lower in nonstarved rats fed starch and maltose than in rats fed glucose, sucrose, or glucose and fructose.	Maltose	75-82	glucose-6-phosphatase catalytic subunit 1	Rattus norvegicus	0-21
3086670-5	1986	It was also determined that the DEX genes (which control dextrin hydrolysis in S. diastaticus), MAL5 (a gene once thought to control maltose metabolism in yeast) and the STA genes are allelic to each other in the following manner: STA1 and DEX2, STA1 and MAL5, and STA2 and DEX1 and STA3 and DEX3.	Maltose	133-140	Wsc2p	Saccharomyces cerevisiae S288C	283-287
2419310-3	1986	Starch hydrolysis with this beta-amylase produces maltose, not glucose, whereas maltotriose and cycloheptaose are resistant to the action of this beta-amylase.	Maltose	50-57	1,4-alpha-D-glucan maltohydrolase	Hordeum vulgare	28-40
3881423-8	1985	Both glucosidase II and neutral alpha-glucosidase AB are high-molecular mass (greater than 200,000 dalton) anionic glycoproteins which bind to concanavalin A, have a broad pH optima (5.5-8.5), and have a similar Km for maltose (4.8 versus 2.1 mM) and the artificial substrate 4-methylumbelliferyl-alpha-D-glucopyranoside (35 versus 19 microM).	Maltose	219-226	glucosidase II alpha subunit	Homo sapiens	24-52
6394601-5	1984	The alpha-glucosidase showed relatively high activity not only toward maltose but also toward alpha-glucans, such as soluble starch, beta-limit dextrin, amylopectin, shellfish glycogen, and amylose.	Maltose	70-77	sucrase-isomaltase	Homo sapiens	4-21
6394601-17	1984	From these results, it was concluded that rabbit muscle acid alpha-glucosidase attacks maltose and glycogen by a single active site mechanism.	Maltose	87-94	sucrase-isomaltase	Homo sapiens	61-78
24186091-4	1982	However, sst1 strains still exhibited trehalose accumulation during growth on maltose medium, provided they contained a gene for maltose fermentation (MAL gene).	Maltose	78-85	aspartyl protease BAR1	Saccharomyces cerevisiae S288C	9-13
18548668-0	1983	An immobilized two-enzyme system (fungal alpha-amylase/glucoamylase) and its use in the continuous production of high conversion maltose-containing corn syrups.	Maltose	129-136	alpha-amylase	Zea mays	41-54
6315410-0	1983	The periplasmic maltose-binding protein modifies the channel-forming characteristics of maltoporin.	Maltose	16-23	maltoporin	Escherichia coli	88-98
6315410-8	1983	The action of maltose-binding protein is highly asymmetrical, and its affinity to maltoporin is very high (KD = 1.5 X 10(-7) M).	Maltose	14-21	maltoporin	Escherichia coli	82-92
7042050-7	1982	Plasma insulin was elevated less after maltose than after glucose infusion.	Maltose	39-46	insulin	Homo sapiens	7-14
6609717-6	1984	Maltose (0.5 M), a competitive inhibitor of alpha-amylase, caused dissociation of the red kidney bean alpha-amylase inhibitor--alpha-amylase complex.	Maltose	0-7	alpha amylase	Bos taurus	44-57
6609717-6	1984	Maltose (0.5 M), a competitive inhibitor of alpha-amylase, caused dissociation of the red kidney bean alpha-amylase inhibitor--alpha-amylase complex.	Maltose	0-7	alpha amylase	Bos taurus	102-115
6609717-6	1984	Maltose (0.5 M), a competitive inhibitor of alpha-amylase, caused dissociation of the red kidney bean alpha-amylase inhibitor--alpha-amylase complex.	Maltose	0-7	alpha amylase	Bos taurus	102-115
6204606-14	1983	In contrast, M-G catalysed the hydrolysis of starch, amylose and maltose with a Km of 3.12 mM, 7.59 mM and 3.52 mM respectively, and had no action on sucrose or palatinose.	Maltose	65-72	maltase-glucoamylase	Homo sapiens	13-16
6415880-1	1983	It is shown that segmented polyurethanes with D-lactose and D-maltose residues in the main polymer chain are subjected to a specific effect of enzymes: beta-galactosidase and alpha-amylase, respectively.	Maltose	60-69	galactosidase beta 1	Homo sapiens	152-170
6355365-3	1983	In the first step of the assay of neutral alpha-glucosidase, glucose was liberated from maltose (citrate-phosphate buffer, pH 6.8, 20 mmol/l maltose, 25 mmol/l turanose).	Maltose	88-95	sucrase-isomaltase	Homo sapiens	42-59
6355365-5	1983	In the first step of the acid alpha-glucosidase assay, glucose was liberated from maltose (citrate-phosphate buffer, pH 3.8, 50 mmol/l maltose, 2 mol/l potassium chloride).	Maltose	82-89	sucrase-isomaltase	Homo sapiens	30-47
6867011-7	1983	Of the disaccharides tested, only maltose stimulated the release of GIP.	Maltose	34-41	GIP	Canis lupus familiaris	68-71
6353754-4	1983	Both forms of neutral alpha-glucosidase I and 2 from human urine exhibited the maximal activity at pH 5.75 = 6.5, had a similar Km value (0.73 mM) with maltose as a substrate and did not differ in their properties from the corresponding forms of neutral alpha-glucosidase in a soluble fraction from human kidney.	Maltose	152-159	sucrase-isomaltase	Homo sapiens	22-39
24173278-5	1983	This isolate, designated MGT1, has a defect in maltose transport (malT1), detected by its markedly lower uptake of [(14)C]maltose, and by its growth on media containing 10% but not 2% maltose.	Maltose	47-54	methylated-DNA--protein-cysteine methyltransferase	Saccharomyces cerevisiae S288C	25-29
24173278-5	1983	This isolate, designated MGT1, has a defect in maltose transport (malT1), detected by its markedly lower uptake of [(14)C]maltose, and by its growth on media containing 10% but not 2% maltose.	Maltose	122-129	methylated-DNA--protein-cysteine methyltransferase	Saccharomyces cerevisiae S288C	25-29
24173278-5	1983	This isolate, designated MGT1, has a defect in maltose transport (malT1), detected by its markedly lower uptake of [(14)C]maltose, and by its growth on media containing 10% but not 2% maltose.	Maltose	122-129	methylated-DNA--protein-cysteine methyltransferase	Saccharomyces cerevisiae S288C	25-29
24186091-4	1982	However, sst1 strains still exhibited trehalose accumulation during growth on maltose medium, provided they contained a gene for maltose fermentation (MAL gene).	Maltose	129-136	aspartyl protease BAR1	Saccharomyces cerevisiae S288C	9-13
6803351-1	1982	Inhibition of microbial enzymes in human dental plaque catalyzing the cleavage of the disaccharides maltose, sucrose and lactose was carried out with the alpha-glucosidase inhibitor, acarbose.	Maltose	100-107	sucrase-isomaltase	Homo sapiens	154-171
6804453-6	1982	The alpha-glucosidase readily hydrolyzed maltose, starch, and glycogen, producing only glucose.	Maltose	41-48	sucrase-isomaltase	Homo sapiens	4-21
24310138-4	1980	alpha-Glucosidase I readily hydrolyzed maltose, isomaltose, kojibiose, maltotriose, panose, amylose, soluble starch, amylopectin and glycogen.	Maltose	39-46	alpha-glucosidase	Beta vulgaris subsp. vulgaris	0-17
6176218-6	1982	The hydrolysis of maltose, trehalose and melezitose confirmed the presence of alpha-glucosidase activity.	Maltose	18-25	sucrase-isomaltase	Homo sapiens	78-95
7050624-0	1982	Suppression of maltose-negative phenotype by a specific nuclear gene (PMU1) in the petite cells of the yeast Saccharomyces cerevisiae.	Maltose	15-22	putative phosphomutase	Saccharomyces cerevisiae S288C	70-74
7050624-5	1982	We have designated this nuclear gene as the PMU1 gene (petite maltose utilizer).	Maltose	62-69	putative phosphomutase	Saccharomyces cerevisiae S288C	44-48
7050624-6	1982	The functional form of the PMU1 gene is required in addition to the MAL4 gene for both constitutive maltase synthesis and maltose utilization in cytoplasmic petite cells derived from strain 1403-7A-P1.	Maltose	122-129	putative phosphomutase	Saccharomyces cerevisiae S288C	27-31
7012112-0	1981	Reconstitution of maltose transport in malB mutants of Escherichia coli through calcium-induced disruptions of the outer membrane.	Maltose	18-25	maltoporin	Escherichia coli	39-43
6169675-1	1981	Maltose, malto-oligosaccharides and their reduced sugar analogues have been tested as substrates and inhibitors of human salivary alpha-amylase and small intestine alpha-glucosidases.	Maltose	0-7	amylase alpha 1A	Homo sapiens	121-143
7000976-0	1980	Effect of maltose on the electroencephalogram of insulin-induced hypoglycemia in rabbits.	Maltose	10-17	insulin	Oryctolagus cuniculus	49-56
6988455-0	1980	The effect of insulin on the metabolism of parenteral maltose in man.	Maltose	54-61	insulin	Homo sapiens	14-21
24310138-5	1980	alpha-Glucosidase II also hydrolyzed maltose, kojibiose and maltotriose but hydrolyzed the other substrates only very weakly or not at all.	Maltose	37-44	alpha-glucosidase	Beta vulgaris subsp. vulgaris	0-17
7005623-1	1980	The previously isolated recessive mutant allele hex2-3 of Saccharomyces cerevisiae caused a defect in carbon catabolite repression of maltase, invertase, malate dehydrogenase, and respiration but at the same time led to an extreme sensitivity to maltose (Zimmerman and Scheel, 1977; Entian and Zimmermann, 1980).	Maltose	246-253	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	48-52
7005623-2	1980	Addition of maltose to a growing culture of a hex2-3 mutant resulted within 60 to 90 min in an inhibition of growth, glycolysis, and de novo protein synthesis.	Maltose	12-19	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	46-50
7005623-5	1980	This abnormal behavior is interpreted as a result of an uncontrolled maltose uptake in hex2 mutants, which in combination with increasing maltase activity results in an accumulation of intracellular glucose.	Maltose	69-76	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	87-91
396048-0	1979	[Nuclear insulin assay after a starch and maltose load in chronic diseases of the pancreas: a preliminary note (author"s transl)].	Maltose	42-49	insulin	Homo sapiens	9-16
790385-1	1976	We have isolated a series of strains in which the lacZ gene has been fused to one of the maltose operons, such that the synthesis of beta-galactosidase (beta-D-galactoside galactohydrolase; EC 3.2.1.23) is inducible by maltose.	Maltose	89-96	galactosidase beta 1	Homo sapiens	133-151
94928-1	1979	The author reports a modification of the UV method UltraZyme Plus alpha-Amyl Harleco and the adaptation to the Eppendorf Enzymautomat 5010. alpha-amylase acts on an oligosaccharide mixture yielding maltose, which is hydrolysed by alpha-glucosidase.	Maltose	198-205	sucrase-isomaltase	Homo sapiens	230-247
346569-0	1978	Permease-specific mutations in Salmonella typhimurium and Escherichia coli that release the glycerol, maltose, melibiose, and lactose transport systems from regulation by the phosphoenolpyruvate:sugar phosphotransferase system.	Maltose	102-109	permease	Escherichia coli	0-8
926710-2	1977	In this method after neutral deproteinization the assay is carried out by the hexokinase technique [6--7] after splitting of the maltose with alpha-glucosidase [8].	Maltose	129-136	sucrase-isomaltase	Homo sapiens	142-159
911942-7	1977	The anomeric configuration of glucose produced under the action of alpha-glucosidase on maltose and starch was determined using a kinetic method.	Maltose	88-95	sucrase-isomaltase	Homo sapiens	67-84
197390-8	1977	Mutants in one gene had reduced hexokinase activities, the other class, located in a centromere linked gene, had elevated hexokinase levels and was inhibited by maltose.	Maltose	161-168	hexokinase	Saccharomyces cerevisiae S288C	122-132
557038-2	1977	The oxidation of UDP-glucose by the enzyme UDP-glucose dehydrogenase (EC 1.1.1.22) from beef liver has been shown to proceed via the enzyme-bound intermediate, UDP-alpha-D-glyco-hexodialdose.	Maltose	164-172	UDP-glucose 6-dehydrogenase	Homo sapiens	43-68
848950-1	1977	Addition of 2 mg of Pb2+/g of soil concident with or after amendment with starch or maltose resulted in 75 and 50% decreases in net synthesis of amylase and alpha-glucosidase, respectively.	Maltose	84-91	sucrase-isomaltase	Homo sapiens	157-174
896090-3	1977	Maltose, trehalose, sucrose, and turanose refeeding resulted in G6PD and ME responses which were higher than the responses to their component monosaccharides (disaccharide effect).	Maltose	0-7	glucose-6-phosphate dehydrogenase	Rattus norvegicus	64-68
369619-7	1978	The isotope effect for alpha-glucosidase is equal to 1, for exogluconase 1,1 for glycogen and 1,18 for maltose.	Maltose	103-110	maltase-glucoamylase	Bos taurus	23-40
26926-4	1978	Antisera have been obtained to bovine serum albumin conjugates containing reductively aminated cellobiose, lactose, and maltose.	Maltose	120-127	albumin	Homo sapiens	38-51
790385-1	1976	We have isolated a series of strains in which the lacZ gene has been fused to one of the maltose operons, such that the synthesis of beta-galactosidase (beta-D-galactoside galactohydrolase; EC 3.2.1.23) is inducible by maltose.	Maltose	219-226	galactosidase beta 1	Homo sapiens	133-151
1245460-1	1976	The gal3 mutation of Saccharomyces, which is associated with an impairment in the utilization of galactose, has been shown to be pleiotropic, causing similar impairments in the utilization of melibiose and maltose.	Maltose	206-213	transcriptional regulator GAL3	Saccharomyces cerevisiae S288C	4-8
825413-2	1976	The Amy4,6 strain has higher enzyme activity than Amy1 strain.-Maltose has the same nutritional value as starch.- The effect of starch in pure culture depends on the yeast level.	Maltose	63-70	drug-responsive transcription factor PDR1	Saccharomyces cerevisiae S288C	50-54
825413-4	1976	The strains do not differ in survival or mean dry weight in pure culture.--In mixed cultures at 50% input of Amy4,6 and Amy1 as larvae the percentage Amy4,6 in adults is present with increasing maltose at low yeast levels in mixed culture.	Maltose	194-201	drug-responsive transcription factor PDR1	Saccharomyces cerevisiae S288C	120-124
1245460-3	1976	The fermentation of maltose and the induction of alpha-glucosidase are regulated independently of the i, c, GAL4 system.	Maltose	20-27	galactose-responsive transcription factor GAL4	Saccharomyces cerevisiae S288C	108-112
235105-4	1975	The results suggest that maltose is hydrolysed in parotid saliva by the salivary alpha-amylase and in dental plaque by enzymes from sources other than the salivary glands, probably microorganisms.	Maltose	25-32	amylase alpha 1A	Homo sapiens	72-94
1156368-4	1975	The 6-O-alkyl-D-galactoses, like the other nontransported C-4 and C-6 derivatives, maltose and 4,6-O-ethylidene-D-glucose, protect against fluorodinitrobenzene inactivation, whereas propyl beta-D-glucopyranoside stimulates the inactivation.	Maltose	83-90	complement C4A (Rodgers blood group)	Homo sapiens	58-61
1156368-4	1975	The 6-O-alkyl-D-galactoses, like the other nontransported C-4 and C-6 derivatives, maltose and 4,6-O-ethylidene-D-glucose, protect against fluorodinitrobenzene inactivation, whereas propyl beta-D-glucopyranoside stimulates the inactivation.	Maltose	83-90	complement C6	Homo sapiens	66-69
818591-6	1975	Serum insulin did rise during maltose infusion.	Maltose	30-37	insulin	Homo sapiens	6-13
4476353-2	1974	The insulin response and growth hormone reaction to continuous administration of glucose and maltose].	Maltose	93-100	insulin	Homo sapiens	4-11
4724583-6	1973	After pretreatment of the lysosomes with cortisone, substrate (maltose) binding to the soluble lysosomal acid alpha-glucosidase is not affected, but the steroid does increase the V(max.)	Maltose	63-70	alpha glucosidase	Rattus norvegicus	105-127
33978737-4	2021	With model maltooligosaccharides G2 (maltose) to G7, the Amyrel reaction starts by a disproportionation leading to Gn-1 and Gn + 1 products, which become themselves substrates for new disproportionation cycles.	Maltose	37-44	amyrel	Drosophila melanogaster	57-63
1112065-2	1975	Liberation of 14-CO-2 from alpha-D,L-(1-14-C) aminoadipate and alpha-(1-14-C) ketoadipate was considerably less in the patient"s fibroblasts than in the patient"s fibroblasts than in normal controls, whereas 14-CO-2 production from (1,5-14-C) glutarate was in the normal range.	Maltose	27-34	complement C2	Homo sapiens	17-21
34003592-6	2021	These supramolecular hydrogels underwent gel-to-sol phase transition upon the addition of alpha-glucosidase as a result of the alpha-glucosidase-catalyzed hydrolysis of the maltose moiety of the amphipathic urea.	Maltose	173-180	sucrase-isomaltase	Homo sapiens	90-107
34003592-6	2021	These supramolecular hydrogels underwent gel-to-sol phase transition upon the addition of alpha-glucosidase as a result of the alpha-glucosidase-catalyzed hydrolysis of the maltose moiety of the amphipathic urea.	Maltose	173-180	sucrase-isomaltase	Homo sapiens	127-144
4676248-0	1972	[Effect of insulin on maltose metabolism].	Maltose	22-29	insulin	Homo sapiens	11-18
5497879-3	1970	With the maltose hydrolysis assay, in some neuromuscular diseases, muscle AM activity can be as low as in heterozygous AM deficiency.	Maltose	9-16	alpha glucosidase	Homo sapiens	74-76
5409938-0	1970	Effect of insulin on the metabolism of circulating maltose.	Maltose	51-58	insulin	Homo sapiens	10-17
5357017-8	1969	Additional evidence for non-penetration of maltose was obtained by demonstrating that the latency of lysosomal alpha-glucosidase is independent of substrate concentration employed.	Maltose	43-50	alpha glucosidase	Rattus norvegicus	101-128
34053560-3	2021	The XRD and DSC were also implemented in maltose crystallization characterization and validated the CCA analysis.	Maltose	41-48	desmocollin 3	Homo sapiens	12-15
34053560-4	2021	The results indicated that CCA could effectively recognize maltose crystals (R = 0.9942), and amorphous maltose mainly crystallized to anhydrate alpha-maltose and beta-maltose monohydrate according to its morphological aspects measured by CCA, XRD, and DSC.	Maltose	104-111	desmocollin 3	Homo sapiens	253-256
33432316-4	2021	MBP-ScFv proves to be a valuable modular platform to synergistically bind maltose-derivatized therapeutic cargos through the MBP, while preserving the targeting competences provided by the ScFv.	Maltose	74-81	myelin basic protein	Homo sapiens	0-3
33554997-3	2021	Using cyclodextrin glucanotransferase to catalyse reversible transglycosylation, and 1-adamantane carboxylic acid as the template, we can synthesise beta-CD from maltose in approximately 70% yield.	Maltose	162-169	ACD shelterin complex subunit and telomerase recruitment factor	Homo sapiens	149-156
33432316-4	2021	MBP-ScFv proves to be a valuable modular platform to synergistically bind maltose-derivatized therapeutic cargos through the MBP, while preserving the targeting competences provided by the ScFv.	Maltose	74-81	immunglobulin heavy chain variable region	Homo sapiens	4-8
33432316-4	2021	MBP-ScFv proves to be a valuable modular platform to synergistically bind maltose-derivatized therapeutic cargos through the MBP, while preserving the targeting competences provided by the ScFv.	Maltose	74-81	myelin basic protein	Homo sapiens	125-128
33432316-4	2021	MBP-ScFv proves to be a valuable modular platform to synergistically bind maltose-derivatized therapeutic cargos through the MBP, while preserving the targeting competences provided by the ScFv.	Maltose	74-81	immunglobulin heavy chain variable region	Homo sapiens	189-193
33432316-5	2021	The methodology has been tested by using a mutated maltose-binding protein (MBP I334W) with an enhanced affinity toward maltose and an ScFv coding sequence toward the human epidermal growth factor receptor 2 (HER2).	Maltose	51-58	myelin basic protein	Homo sapiens	76-79
33432316-5	2021	The methodology has been tested by using a mutated maltose-binding protein (MBP I334W) with an enhanced affinity toward maltose and an ScFv coding sequence toward the human epidermal growth factor receptor 2 (HER2).	Maltose	51-58	erb-b2 receptor tyrosine kinase 2	Homo sapiens	173-207
33432316-5	2021	The methodology has been tested by using a mutated maltose-binding protein (MBP I334W) with an enhanced affinity toward maltose and an ScFv coding sequence toward the human epidermal growth factor receptor 2 (HER2).	Maltose	51-58	erb-b2 receptor tyrosine kinase 2	Homo sapiens	209-213
33650638-1	2021	Maltose, the major product of starch breakdown in Arabidopsis (Arabidopsis thaliana) leaves, exits the chloroplast via the maltose transporter MEX1.	Maltose	0-7	root cap 1 (RCP1)	Arabidopsis thaliana	143-147
33650638-2	2021	Consequently, mex1 loss-of-function plants exhibit substantial maltose accumulation, a starch-excess phenotype and a specific chlorotic phenotype during leaf development.	Maltose	63-70	root cap 1 (RCP1)	Arabidopsis thaliana	14-18
33650638-7	2021	These findings point to a threshold level of maltose responsible for the marked developmental defects in mex1.	Maltose	45-52	root cap 1 (RCP1)	Arabidopsis thaliana	105-109
33650638-9	2021	In summary, these results demonstrate the possibility to bypass the MEX1 transporter, allow us to differentiate between possible starch-excess and maltose-excess responses, and demonstrate that stromal maltose accumulation prevents frost defects.	Maltose	202-209	root cap 1 (RCP1)	Arabidopsis thaliana	68-72
32617844-8	2020	Through experimental research and analysis, it was identified that the glucose-sucrose-maltose medium was the beneficial medium to the enrichment of butyric acid-producing bacteria, and the high-throughput sequencing determined that the enriched genera were Clostridium spp.	Maltose	87-94	histocompatibility minor 13	Homo sapiens	270-273
33539092-0	2021	Maltose-Based Fluorinated Surfactants for Membrane-Protein Extraction and Stabilization.	Maltose	0-7	membrane protein	Escherichia coli	42-58
33576408-4	2021	METHOD: Non-resistant (digestible) starch is hydrolysed to glucose and maltose by pancreatic alpha-amylase and amyloglucosidase at pH 6.0 with shaking or stirring at 37  C for 4 h. Sucrose, lactose, maltose and isomaltose are completely hydrolyzed by specific enzymes to their constituent monosaccharides, which are then measured using pure enzymes in a single reaction cuvette.	Maltose	71-78	amylase alpha 2A	Homo sapiens	82-106
33576408-4	2021	METHOD: Non-resistant (digestible) starch is hydrolysed to glucose and maltose by pancreatic alpha-amylase and amyloglucosidase at pH 6.0 with shaking or stirring at 37  C for 4 h. Sucrose, lactose, maltose and isomaltose are completely hydrolyzed by specific enzymes to their constituent monosaccharides, which are then measured using pure enzymes in a single reaction cuvette.	Maltose	199-206	amylase alpha 2A	Homo sapiens	82-106
33008588-8	2020	First, we demonstrated our strategy using maltose-binding protein-fused green fluorescent protein (MBP-GFP) to model an acidic protein.	Maltose	42-49	myelin basic protein	Homo sapiens	99-102
32617844-9	2020	Glucose-sucrose-maltose medium experimental data confirmed that the decrease of CO2 and H2 daily yield, the increase of butyric acid concentration, and the decrease of pH value had a significant positive correlation with the enrichment of Clostridium spp.	Maltose	16-23	histocompatibility minor 13	Homo sapiens	251-254
32578583-3	2020	Here, by utilising the binding of maltose to hydrogels constructed from photo-chemically cross-linked maltose binding protein (MBP), we investigate the effects of protein stabilisation at the molecular level on the macroscopic mechanical and structural properties of a protein-based hydrogel.	Maltose	34-41	myelin basic protein	Homo sapiens	127-130
32111129-1	2020	The quantitation of sugars, including glucose, the primary fermentable sugar; maltose (DP2); and maltotriose (DP3), is a standard procedure during the corn-to-ethanol fermentation process.	Maltose	78-85	diphosphonucleotide phosphatase 2	Zea mays	87-90
32578583-3	2020	Here, by utilising the binding of maltose to hydrogels constructed from photo-chemically cross-linked maltose binding protein (MBP), we investigate the effects of protein stabilisation at the molecular level on the macroscopic mechanical and structural properties of a protein-based hydrogel.	Maltose	102-109	myelin basic protein	Homo sapiens	127-130
32578583-4	2020	Rheological measurements show an enhancement in the mechanical strength and energy dissipation of MBP hydrogels in the presence of maltose.	Maltose	131-138	myelin basic protein	Homo sapiens	98-101
31953836-8	2020	The largest increases in 3-DG concentrations were observed in the maltose-lysine systems (24.94 to 35.74 mug mL-1 ).	Maltose	66-73	L1 cell adhesion molecule	Mus musculus	109-113
32577653-3	2020	To this end, we created a construct expressing recombinant N fused to a N-terminal maltose binding protein tag which helps keep the oligomeric N soluble for purification.	Maltose	83-90	nucleocapsid phosphoprotein	Severe acute respiratory syndrome coronavirus 2	72-73
32577653-3	2020	To this end, we created a construct expressing recombinant N fused to a N-terminal maltose binding protein tag which helps keep the oligomeric N soluble for purification.	Maltose	83-90	nucleocapsid phosphoprotein	Severe acute respiratory syndrome coronavirus 2	72-73
32260465-4	2020	The crp-deficient mutant lost the capacity to utilize maltose, and showed significantly reduced motility due to the lack of flagella synthesis.	Maltose	54-61	c-reactive protein, pentraxin-related	Danio rerio	4-7
31074585-7	2019	At last, the resultant (+)-DCDs (700 microg mL-1 ) are employed to modify maltase in an effort to regulate the hydrolytic rate of maltose, showing an excellent inhibition ratio to maltase of 54.7%, significantly higher than that of (-)-LCDs (15.5%) in the same reaction conditions.	Maltose	130-137	L1 cell adhesion molecule	Mus musculus	44-48
33654738-4	2020	MBP-PKD1-5 is a fusion of the maltose binding protein with all five of the PKD domains of the AAVR receptor.	Maltose	30-37	myelin basic protein	Homo sapiens	0-3
33654738-4	2020	MBP-PKD1-5 is a fusion of the maltose binding protein with all five of the PKD domains of the AAVR receptor.	Maltose	30-37	polycystin 1, transient receptor potential channel interacting	Homo sapiens	4-8
31694180-1	2019	Glycosyltransferase-producing Leuconostoc lactis CCK940 produces CCK- oligosaccharides, gluco-oligosaccharide molecules, using sucrose and maltose as donor and acceptor molecules, respectively.	Maltose	139-146	cholecystokinin	Mus musculus	49-52
31932409-8	2020	These proteins comprise several solute carriers, such as the ATP/ADP antiporter NTT2 (nucleotide transporter 2, substantially increased abundance) or the maltose exporter MEX1 (maltose exporter 1, substantially decreased abundance).	Maltose	154-161	root cap 1 (RCP1)	Arabidopsis thaliana	171-175
31932409-8	2020	These proteins comprise several solute carriers, such as the ATP/ADP antiporter NTT2 (nucleotide transporter 2, substantially increased abundance) or the maltose exporter MEX1 (maltose exporter 1, substantially decreased abundance).	Maltose	154-161	root cap 1 (RCP1)	Arabidopsis thaliana	177-195
31901816-0	2020	Nano co-immobilization of alpha-amylase and maltogenic amylase by nanomagnetic combi-cross-linked enzyme aggregates method for maltose production from corn starch.	Maltose	127-134	alpha-amylase	Zea mays	26-39
31901816-1	2020	Starch hydrolysis to maltose by nano-magnetic combined cross-linked enzyme aggregates of alpha-amylase and maltogenic amylase (NM-Combi-CLEAs) is an important step to open new perspectives for special food and pharmaceutic production.	Maltose	21-28	alpha-amylase	Zea mays	89-102
31744922-6	2019	Gel shift assays confirmed direct regulation of the malT and ptsG promoters, and Crp was then linked to Y. pestis growth on maltose as a sole carbon source.	Maltose	124-131	C-reactive protein, pentraxin-related	Mus musculus	81-84
30753419-4	2019	The results demonstrated that a 2-min oral mastication of starchy chewing gum produced an oral concentration of maltose above the sweet taste threshold and revealed that the total amount of maltose equivalent reducing sugars produced was positively correlated with the sAA activity.	Maltose	112-119	serum amyloid A1 cluster	Homo sapiens	269-272
30950267-3	2019	In previous work, we presented experimental evidence that macromolecular crowders acted competitively in inhibiting the binding of maltose binding protein (MBP) with its ligand maltose.	Maltose	131-138	myelin basic protein	Homo sapiens	156-159
30950267-3	2019	In previous work, we presented experimental evidence that macromolecular crowders acted competitively in inhibiting the binding of maltose binding protein (MBP) with its ligand maltose.	Maltose	177-184	myelin basic protein	Homo sapiens	156-159
30950267-5	2019	Maltose binds to the cleft between two lobes of MBP, and in a series of mutants, the affinities increased with an increase in the extent of lobe closure.	Maltose	0-7	myelin basic protein	Homo sapiens	48-51
30950267-8	2019	Competition between the ligand and crowder, as indicated by fitting of titration data and directly by nuclear magnetic resonance spectroscopy, and their similar preferences for closed MBP conformations further suggest the scenario in which the crowder, like maltose, preferentially binds to the interlobe cleft of MBP.	Maltose	258-265	myelin basic protein	Homo sapiens	184-187
30950267-8	2019	Competition between the ligand and crowder, as indicated by fitting of titration data and directly by nuclear magnetic resonance spectroscopy, and their similar preferences for closed MBP conformations further suggest the scenario in which the crowder, like maltose, preferentially binds to the interlobe cleft of MBP.	Maltose	258-265	myelin basic protein	Homo sapiens	314-317
31509948-5	2019	Despite the robust alteration in the gut microbiome in DIO mice, co-administration of maltose and the alpha-glucosidase inhibitor (alpha-GI) miglitol induced the microbiome-mediated suppression of GIP secretion.	Maltose	86-93	gastric inhibitory polypeptide	Mus musculus	197-200
31266901-9	2019	Nighttime maltose levels are reduced in lsf1, and genetic analysis indicated that the starch-excess phenotype of lsf1 is dependent on bam1 and bam3 We propose that LSF1 binds beta-amylases at the starch granule surface, thereby promoting starch degradation.	Maltose	10-17	like SEX4 1	Arabidopsis thaliana	40-44
31266901-9	2019	Nighttime maltose levels are reduced in lsf1, and genetic analysis indicated that the starch-excess phenotype of lsf1 is dependent on bam1 and bam3 We propose that LSF1 binds beta-amylases at the starch granule surface, thereby promoting starch degradation.	Maltose	10-17	like SEX4 1	Arabidopsis thaliana	164-168
30895774-0	2019	Colorimetric Detection of Salivary alpha-Amylase Using Maltose as a Noncompetitive Inhibitor for Polysaccharide Cleavage.	Maltose	55-62	amylase alpha 1A	Homo sapiens	26-48
30753419-4	2019	The results demonstrated that a 2-min oral mastication of starchy chewing gum produced an oral concentration of maltose above the sweet taste threshold and revealed that the total amount of maltose equivalent reducing sugars produced was positively correlated with the sAA activity.	Maltose	190-197	serum amyloid A1 cluster	Homo sapiens	269-272
31560984-0	2019	An integrated transport mechanism of the maltose ABC importer.	Maltose	41-48	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	49-52
30874698-2	2019	An ionic liquid (IL) was explored in this study as a promising reaction medium for the maltose glycation of soy protein isolate (SPI) to decrease water activity and to shift the reaction equilibrium.	Maltose	87-94	chromogranin A	Homo sapiens	129-132
30874698-4	2019	Using the four conditions, two glycated SPI products, namely GSPI-I and GSPI-II with maltose contents of 19.88 and 6.26 g kg-1 protein, were prepared with this IL and water, respectively.	Maltose	85-92	chromogranin A	Homo sapiens	40-43
30409636-6	2019	Since the action of already known plant beta-amylases (sweet potato and soybean) on native starch granule is not very effective and requires gelatinization for maltose production, beta-amylase from peanut could be a useful alternative in the present endeavor.	Maltose	160-167	beta-amylase	Glycine max	40-52
30990119-6	2019	Dramatically increase in EPO expression in conjugated linoleic acid, spermidine, trehalose, and maltose (19, 20, 16, and 19-fold, respectively) did not increase erythropoietin productivity, but betaine which did not caused ER expansion, with minor increase in EPO gene expression increase EPO productivity.	Maltose	96-103	erythropoietin	Cricetulus griseus	25-28
31560984-2	2019	A combination of biochemical, biophysical, and structural studies has established the maltose transporter MalFGK2 as one of the best-characterized proteins of the ABC family.	Maltose	86-93	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	163-166
30340690-4	2018	The sAA concentration levels were determined based on the detection of maltose produced by enzymatic hydrolysis of starch.	Maltose	71-78	amylase alpha 1A	Homo sapiens	4-7
30400014-2	2018	However, we found that mice exhibit opposite secretory responses in response to co-administration of maltose plus an alpha-glucosidase inhibitor miglitol (maltose/miglitol), stimulatory for GLP-1, as reported previously, but inhibitory for GIP.	Maltose	101-108	glucagon	Mus musculus	190-195
30220548-5	2018	In the present study, we developed an anti-FSHR polyclonal serum by using a 14-kDa peptide conjugated to maltose binding protein.	Maltose	105-112	follicle stimulating hormone receptor	Bos taurus	43-47
30400014-2	2018	However, we found that mice exhibit opposite secretory responses in response to co-administration of maltose plus an alpha-glucosidase inhibitor miglitol (maltose/miglitol), stimulatory for GLP-1, as reported previously, but inhibitory for GIP.	Maltose	101-108	gastric inhibitory polypeptide	Mus musculus	240-243
30400014-2	2018	However, we found that mice exhibit opposite secretory responses in response to co-administration of maltose plus an alpha-glucosidase inhibitor miglitol (maltose/miglitol), stimulatory for GLP-1, as reported previously, but inhibitory for GIP.	Maltose	155-162	glucagon	Mus musculus	190-195
30400014-3	2018	Gut microbiota was shown to be involved in maltose/miglitol-induced GIP suppression, as the suppression was attenuated in antibiotics (Abs)-treated mice and abolished in germ-free mice.	Maltose	43-50	gastric inhibitory polypeptide	Mus musculus	68-71
30400014-5	2018	GIP suppression by maltose/miglitol was not observed in mice lacking a SCFA receptor Ffar3, but it was normally seen in Ffar2-deficient mice.	Maltose	19-26	gastric inhibitory polypeptide	Mus musculus	0-3
29851467-5	2018	The MBP binding site is loaded with dye or drug conjugates of the maltose analogue beta-cyclodextrin (betaCD) to yield a QD-MBP-betaCD ensemble conjugate.	Maltose	66-73	myelin basic protein	Homo sapiens	4-7
30004675-5	2018	Even in its MG state, MBP is known to still bind its ligand maltose.	Maltose	60-67	myelin basic protein	Homo sapiens	22-25
30004675-12	2018	Measurements show a defined structure around the binding pocket of MBP in MG, which explains maltose binding.	Maltose	93-100	myelin basic protein	Homo sapiens	67-70
30004675-13	2018	A new and important finding is that in both states ligand-free MBP can be found in open and closed form, while ligand-bound MBP appears only in closed form because of maltose binding.	Maltose	167-174	myelin basic protein	Homo sapiens	124-127
29936578-0	2018	Overexpression of SNF4 and deletions of REG1- and REG2-enhanced maltose metabolism and leavening ability of baker"s yeast in lean dough.	Maltose	64-71	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	40-44
29936578-0	2018	Overexpression of SNF4 and deletions of REG1- and REG2-enhanced maltose metabolism and leavening ability of baker"s yeast in lean dough.	Maltose	64-71	protein phosphatase regulator REG2	Saccharomyces cerevisiae S288C	50-54
29936578-3	2018	Results revealed that SNF4 overexpression and REG1 and REG2 deletions effectively alleviated glucose repression at different levels, thereby enhancing maltose metabolism and leavening ability to varying degrees.	Maltose	151-158	AMP-activated serine/threonine-protein kinase regulatory subunit SNF4	Saccharomyces cerevisiae S288C	22-26
29936578-3	2018	Results revealed that SNF4 overexpression and REG1 and REG2 deletions effectively alleviated glucose repression at different levels, thereby enhancing maltose metabolism and leavening ability to varying degrees.	Maltose	151-158	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	46-50
29936578-3	2018	Results revealed that SNF4 overexpression and REG1 and REG2 deletions effectively alleviated glucose repression at different levels, thereby enhancing maltose metabolism and leavening ability to varying degrees.	Maltose	151-158	protein phosphatase regulator REG2	Saccharomyces cerevisiae S288C	55-59
29936578-5	2018	The overexpressed SNF4 with deleted REG1 and REG2 mutant DeltaREG1DeltaREG2 + SNF4 displayed the highest maltose metabolism and strongest leavening ability under the test conditions.	Maltose	105-112	AMP-activated serine/threonine-protein kinase regulatory subunit SNF4	Saccharomyces cerevisiae S288C	18-22
29936578-5	2018	The overexpressed SNF4 with deleted REG1 and REG2 mutant DeltaREG1DeltaREG2 + SNF4 displayed the highest maltose metabolism and strongest leavening ability under the test conditions.	Maltose	105-112	protein phosphatase regulator REG2	Saccharomyces cerevisiae S288C	45-49
29936578-5	2018	The overexpressed SNF4 with deleted REG1 and REG2 mutant DeltaREG1DeltaREG2 + SNF4 displayed the highest maltose metabolism and strongest leavening ability under the test conditions.	Maltose	105-112	AMP-activated serine/threonine-protein kinase regulatory subunit SNF4	Saccharomyces cerevisiae S288C	78-82
29729336-6	2018	This enzyme has high hydrolysis rate toward corn, wheat and potato starch and hydrolyzes soluble starch to glucose, maltose, maltotriose and maltotetraose, indicating that the alpha-amylase represents a promising candidate for applications in the food industry.	Maltose	116-123	alpha-amylase	Solanum tuberosum	176-189
29621479-9	2018	In support of this possibility, we reported that acarbose (an alpha-glucosidase inhibitor) prevented sucrose, maltose and Polycose from eliciting CPIR.	Maltose	110-117	sucrase isomaltase (alpha-glucosidase)	Mus musculus	62-79
29601965-4	2018	In order to be able to produce large quantities of the extracellular moiety of human CD74, which has been reported to be unstable and protease-sensitive, different constructs were made as fusions with two solubility enhancers: the well-known maltose-binding domain and Fh8, a small protein secreted by the parasite Fasciola hepatica.	Maltose	242-249	CD74 molecule	Homo sapiens	85-89
29851467-7	2018	Microplate-based FRET assays demonstrated that the betaCD conjugate was released from the MBP binding pocket by maltose addition with an affinity that matched native MBP-maltose binding interactions.	Maltose	112-119	myelin basic protein	Homo sapiens	90-93
29851467-7	2018	Microplate-based FRET assays demonstrated that the betaCD conjugate was released from the MBP binding pocket by maltose addition with an affinity that matched native MBP-maltose binding interactions.	Maltose	170-177	myelin basic protein	Homo sapiens	166-169
29393538-2	2018	In this study, the extraction condition of beta-amylase from brewer"s malt and the optimal dosage of beta-amylase in maltose syrup production were optimized using response surface methodology and uniform design method.	Maltose	117-124	beta-amylase	Glycine max	101-113
29393538-0	2018	Process optimization of the extraction condition of beta-amylase from brewer"s malt and its application in the maltose syrup production.	Maltose	111-118	beta-amylase	Glycine max	52-64
29393538-1	2018	beta-Amylase is of important biotechnological aid in maltose syrup production.	Maltose	53-60	beta-amylase	Glycine max	0-12
29393538-2	2018	In this study, the extraction condition of beta-amylase from brewer"s malt and the optimal dosage of beta-amylase in maltose syrup production were optimized using response surface methodology and uniform design method.	Maltose	117-124	beta-amylase	Glycine max	43-55
29393538-4	2018	The optimal dosages of beta-amylase used in maltose syrup production were 455.67 U g-1 starch and its application in maltose syrup production led to a 68.37% maltose content in maltose syrup, which was 11.2% and 28.9% higher than those using beta-amylases from soybean and microbe (P < 0.01).	Maltose	44-51	beta-amylase	Glycine max	23-35
29393538-4	2018	The optimal dosages of beta-amylase used in maltose syrup production were 455.67 U g-1 starch and its application in maltose syrup production led to a 68.37% maltose content in maltose syrup, which was 11.2% and 28.9% higher than those using beta-amylases from soybean and microbe (P < 0.01).	Maltose	117-124	beta-amylase	Glycine max	23-35
29393538-4	2018	The optimal dosages of beta-amylase used in maltose syrup production were 455.67 U g-1 starch and its application in maltose syrup production led to a 68.37% maltose content in maltose syrup, which was 11.2% and 28.9% higher than those using beta-amylases from soybean and microbe (P < 0.01).	Maltose	117-124	beta-amylase	Glycine max	23-35
29393538-4	2018	The optimal dosages of beta-amylase used in maltose syrup production were 455.67 U g-1 starch and its application in maltose syrup production led to a 68.37% maltose content in maltose syrup, which was 11.2% and 28.9% higher than those using beta-amylases from soybean and microbe (P < 0.01).	Maltose	117-124	beta-amylase	Glycine max	23-35
29393538-5	2018	Thus, beta-amylase from brewer"s malt was beneficial for production of high maltose syrup.	Maltose	76-83	beta-amylase	Glycine max	6-18
29791979-5	2018	Importantly, the crystal structures of the N-terminal PYD and C-terminal CARD of zebrafish ASC were determined independently as two separate entities fused to maltose-binding protein.	Maltose	159-166	PYD and CARD domain containing	Danio rerio	91-94
29068219-3	2017	For this study, we addressed the recalcitrant expression of BAPT by expressing it as a soluble maltose binding protein fusion (MBP-BAPT).	Maltose	95-102	myelin basic protein	Homo sapiens	127-130
29478547-6	2018	A two-fold difference was found for glycation in the presence of the dimers lactose and maltose for beta-casein but not for the whey proteins.	Maltose	88-95	casein beta	Homo sapiens	100-111
31245723-2	2018	beta-amylase is a crucial enzyme in the beer industry providing maltose for fermenting yeast.	Maltose	64-71	beta-amylase 1, chloroplastic-like	Nicotiana tabacum	0-12
29517411-2	2018	In the present study, we demonstrated that MalR formed a complex with Hsp70 and Hsp90 chaperones under non-inducing conditions similar to the yeast counterpart Mal63 and that the complex was released from the chaperone complex after the addition of the inducer maltose.	Maltose	261-268	Hsp90 family chaperone HSP82	Saccharomyces cerevisiae S288C	80-85
29487277-10	2018	Furthermore, the lack of AtMyb56 resulted in altered accumulation of maltose in a sucrose-dependent manner.	Maltose	69-76	myb domain protein 56	Arabidopsis thaliana	25-32
29487277-11	2018	Therefore, the sucrose responsive AtMyb56 regulates AtGPT2 gene expression in a sucrose-dependent manner to modulate maltose and anthocyanin accumulations in response to the circadian cycle.	Maltose	117-124	myb domain protein 56	Arabidopsis thaliana	34-41
29487277-11	2018	Therefore, the sucrose responsive AtMyb56 regulates AtGPT2 gene expression in a sucrose-dependent manner to modulate maltose and anthocyanin accumulations in response to the circadian cycle.	Maltose	117-124	glucose-6-phosphate/phosphate translocator 2	Arabidopsis thaliana	52-58
29846922-5	2018	Herein we report a method for carrying out a reverse chemical genetic screen on alpha-glucosidase, the enzyme that catalyzes the final step in starch degradation during plant germination, namely the hydrolysis of maltose to release glucose.	Maltose	213-220	sucrase-isomaltase	Homo sapiens	80-97
29121937-0	2017	Functional analysis of the global repressor Tup1 for maltose metabolism in Saccharomyces cerevisiae: different roles of the functional domains.	Maltose	53-60	chromatin-silencing transcriptional regulator TUP1	Saccharomyces cerevisiae S288C	44-48
29121937-3	2017	In this study, we aim to investigate the role of Tup1 and its domains in maltose metabolism of industrial baker"s yeast.	Maltose	73-80	chromatin-silencing transcriptional regulator TUP1	Saccharomyces cerevisiae S288C	49-53
29614773-1	2018	Saccharomyces cerevisiae MCD4 is a 2-deoxyglucose (2-DOG)-resistant mutant derived from the wild-type strain, AK46, wherein the 2-DOG resistance improves the maltose fermentative ability.	Maltose	158-165	mannose-ethanolamine phosphotransferase MCD4	Saccharomyces cerevisiae S288C	25-29
29614773-3	2018	In maltose medium, the expression of MAL11 and MAL31 in MCD4 was 2.1 and 4.2 times significantly higher than that in AK46, respectively.	Maltose	3-10	alpha-glucoside permease	Saccharomyces cerevisiae S288C	37-42
29614773-3	2018	In maltose medium, the expression of MAL11 and MAL31 in MCD4 was 2.1 and 4.2 times significantly higher than that in AK46, respectively.	Maltose	3-10	maltose permease	Saccharomyces cerevisiae S288C	47-52
29614773-3	2018	In maltose medium, the expression of MAL11 and MAL31 in MCD4 was 2.1 and 4.2 times significantly higher than that in AK46, respectively.	Maltose	3-10	mannose-ethanolamine phosphotransferase MCD4	Saccharomyces cerevisiae S288C	56-60
29614773-6	2018	Since the expression of major catabolite repression-related genes did not show significant differences between MCD4 and AK46, these results showed that the higher maltose fermentative ability of MCD4 is due to the activation of MAL genes encoding two maltose permeases and two alpha-glucosidases.	Maltose	163-170	mannose-ethanolamine phosphotransferase MCD4	Saccharomyces cerevisiae S288C	195-199
29380206-2	2018	In this work, we investigated the interaction of Cytochrome c (Cyt c) with maltoligosaccharides, namely maltose (Mal II), maltotriose (Mal III), maltotetraose (Mal IV), maltopentaose (Mal V), maltohexaose (Mal VI) and maltoheptaose (Mal VII).	Maltose	104-111	cytochrome c, somatic	Homo sapiens	49-61
29380206-2	2018	In this work, we investigated the interaction of Cytochrome c (Cyt c) with maltoligosaccharides, namely maltose (Mal II), maltotriose (Mal III), maltotetraose (Mal IV), maltopentaose (Mal V), maltohexaose (Mal VI) and maltoheptaose (Mal VII).	Maltose	104-111	cytochrome c, somatic	Homo sapiens	63-68
29295923-0	2018	Folding of maltose binding protein outside of and in GroEL.	Maltose	11-18	heat shock protein family D (Hsp60) member 1	Homo sapiens	53-58
29295923-1	2018	We used hydrogen exchange-mass spectrometry (HX MS) and fluorescence to compare the folding of maltose binding protein (MBP) in free solution and in the GroEL/ES cavity.	Maltose	95-102	myelin basic protein	Homo sapiens	120-123
28843936-7	2018	First, maltose was chosen as the substrate for GAA and the generated glucose were immediately utilized by GOx to generate H2O2, and finally, H2O2 etched the Ag nanoprism to round nanodiscs, resulting in the blue shift of surface plasmon resonance (SPR) absorption band.	Maltose	7-14	alpha glucosidase	Homo sapiens	47-50
28843936-7	2018	First, maltose was chosen as the substrate for GAA and the generated glucose were immediately utilized by GOx to generate H2O2, and finally, H2O2 etched the Ag nanoprism to round nanodiscs, resulting in the blue shift of surface plasmon resonance (SPR) absorption band.	Maltose	7-14	hydroxyacid oxidase 1	Homo sapiens	106-109
28887383-5	2017	Using surface plasmon resonance, a tandem P1BS sequence showed ~50-fold higher affinity for MBPAtdPHR1 (a fusion protein comprising the DNA-binding domain and coiled-coil domain of AtPHR1 fused to maltose-binding protein) than a single site.	Maltose	197-204	photolyase 1	Arabidopsis thaliana	181-187
29121937-5	2017	RESULTS: The results suggest that the TUP1 gene is essential to maltose metabolism in industrial baker"s yeast.	Maltose	64-71	chromatin-silencing transcriptional regulator TUP1	Saccharomyces cerevisiae S288C	38-42
29121937-6	2017	Importantly, different domains of Tup1 play different roles in glucose repression and maltose metabolism of industrial baker"s yeast cells.	Maltose	86-93	chromatin-silencing transcriptional regulator TUP1	Saccharomyces cerevisiae S288C	34-38
29121937-7	2017	The Ssn6 interaction, N-terminal repression and C-terminal repression domains might play roles in the regulation of MAL transcription by Tup1 for maltose metabolism of baker"s yeast.	Maltose	146-153	transcription regulator CYC8	Saccharomyces cerevisiae S288C	4-8
29121937-7	2017	The Ssn6 interaction, N-terminal repression and C-terminal repression domains might play roles in the regulation of MAL transcription by Tup1 for maltose metabolism of baker"s yeast.	Maltose	146-153	chromatin-silencing transcriptional regulator TUP1	Saccharomyces cerevisiae S288C	137-141
29040651-0	2017	The Chlamydomonas mex1 mutant shows impaired starch mobilization without maltose accumulation.	Maltose	73-80	uncharacterized protein	Chlamydomonas reinhardtii	18-22
29040651-8	2017	These findings suggest that Mex1 is essential for starch mobilization in both Chlamydomonas and Arabidopsis, and that this protein family may support several functions and not only be restricted to maltose export across the plastidial envelope.	Maltose	198-205	uncharacterized protein	Chlamydomonas reinhardtii	28-32
29084970-1	2017	Mal11 catalyzes proton-coupled maltose transport across the plasma membrane of Saccharomyces cerevisiae.	Maltose	31-38	alpha-glucoside permease	Saccharomyces cerevisiae S288C	0-5
29084970-3	2017	We find that wildtype Mal11 is extremely well coupled and allows yeast to rapidly accumulate maltose to dangerous levels, resulting under some conditions in self-lysis.	Maltose	93-100	alpha-glucoside permease	Saccharomyces cerevisiae S288C	22-27
28570943-4	2017	Using either sucrose or maltose as substrate resveratrol, piceatannol and 3"-hydroxypterostilbene showed strong inhibition of mammalian alpha-glucosidase activity; pinostilbene, cis-desoxyrhapontigenin and trans-desoxyrhapontigenin had moderate inhibition.	Maltose	24-31	sucrase-isomaltase	Homo sapiens	136-153
28576440-0	2017	Photometric assay of maltose and maltose-forming enzyme activity by using 4-alpha-glucanotransferase (DPE2) from higher plants.	Maltose	21-28	disproportionating enzyme 2	Arabidopsis thaliana	102-106
28576440-0	2017	Photometric assay of maltose and maltose-forming enzyme activity by using 4-alpha-glucanotransferase (DPE2) from higher plants.	Maltose	33-40	disproportionating enzyme 2	Arabidopsis thaliana	102-106
28576440-5	2017	In this communication, we present a photometric maltose assay using 4-alpha-glucanotransferase (AtDPE2) from Arabidopsis thaliana.	Maltose	48-55	disproportionating enzyme 2	Arabidopsis thaliana	96-102
28576440-6	2017	Under in vitro conditions, AtDPE2 utilizes maltose as glucosyl donor and glycogen as acceptor releasing the other hexosyl unit as free glucose which is photometrically quantified following enzymatic phosphorylation and oxidation.	Maltose	43-50	disproportionating enzyme 2	Arabidopsis thaliana	27-33
28576440-11	2017	Finally, the AtDPE2-based maltose assay was used to quantify leaf maltose contents of both Arabidopsis wild type and AtDPE2-deficient plants throughout the light-dark cycle.	Maltose	26-33	disproportionating enzyme 2	Arabidopsis thaliana	13-19
28929138-3	2017	We report that maltose binding protein-fused, full-length wild-type MxB purifies as oligomers and further self-assembles into helical arrays in physiological salt.	Maltose	15-22	MX dynamin like GTPase 2	Homo sapiens	68-71
28681602-3	2017	Maltose hydrolysis was reduced (49.6-82.4%, p < 0.05), albeit with high IC50 values (500-940 GAE muM).	Maltose	0-7	latexin	Homo sapiens	100-103
28319816-2	2017	The PEI-Mal-entrapped gold nanoparticles of about 2nm in diameter influence the polyplex formation of the hyperbranched PEI containing bulky maltose, and in consequence the DNA is more compactized in the inner part of spherical polyplex particles of about 150nm in diameter.	Maltose	141-148	mal, T cell differentiation protein	Homo sapiens	8-11
30263598-1	2017	alpha-Glucosidase was immobilized onto an epoxy-activated resin (Eupergit C) to catalyze maltose into isomaltooligosaccharides (IMO), and then the effects of organic-aqueous media on the enzymatic properties of immobilized alpha-glucosidase were examined.	Maltose	89-96	sucrase-isomaltase	Homo sapiens	0-17
28500115-0	2017	Erroneously elevated glucose values due to maltose interference in mutant glucose dehydrogenase pyrroloquinolinequinone (mutant GDH-PQQ) based glucometer.	Maltose	43-50	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	Homo sapiens	74-95
28500115-0	2017	Erroneously elevated glucose values due to maltose interference in mutant glucose dehydrogenase pyrroloquinolinequinone (mutant GDH-PQQ) based glucometer.	Maltose	43-50	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	Homo sapiens	128-131
28500115-8	2017	In this article spuriously high glucose values due to maltose interference in a glucometer using the mutant GDH-PQQ chemistry are being reported.	Maltose	54-61	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	Homo sapiens	108-111
32625476-2	2017	This beta-amylase is intended to be used in the starch processing for maltose syrup production and the manufacture of a Japanese rice cake type.	Maltose	70-77	beta-amylase	Oryza sativa Japonica Group	5-17
28180997-9	2017	The use of a putative lobster SCRT by both maltose and trehalose is nutritionally appropriate for lobsters as they commonly digest glycogen and chitin, polymers of maltose and trehalose, respectively.	Maltose	43-50	Solute carrier family 45 member 1	Drosophila melanogaster	30-34
28482870-9	2017	However, Pfk1 activities of the sfPFKM transformants were detected in maltose medium, but the growth in maltose was possible only after the addition of 10 mM of ethanol to the medium.	Maltose	70-77	6-phosphofructokinase subunit alpha	Saccharomyces cerevisiae S288C	9-13
28482870-11	2017	However, the transformants carrying modified Pfk-M enzymes grew faster than the transformants with the human native human Pfk-M enzyme in a narrow ecological niche with a low maltose concentration medium that was further improved by additional modifications.	Maltose	175-182	phosphofructokinase, muscle	Homo sapiens	45-50
28482870-11	2017	However, the transformants carrying modified Pfk-M enzymes grew faster than the transformants with the human native human Pfk-M enzyme in a narrow ecological niche with a low maltose concentration medium that was further improved by additional modifications.	Maltose	175-182	phosphofructokinase, muscle	Homo sapiens	122-127
28180997-9	2017	The use of a putative lobster SCRT by both maltose and trehalose is nutritionally appropriate for lobsters as they commonly digest glycogen and chitin, polymers of maltose and trehalose, respectively.	Maltose	164-171	Solute carrier family 45 member 1	Drosophila melanogaster	30-34
28225829-2	2017	In Arabidopsis chloroplasts, beta-amylase BAM3 hydrolyses transitory starch, producing maltose and residual maltotriose.	Maltose	87-94	Leucine-rich receptor-like protein kinase family protein	Arabidopsis thaliana	42-46
28322788-3	2017	Three polypeptides spanning the MPF region (MPF1-148, MPF 34-288, MPF/MSLN254-400) were produced in E.coli as maltose-binding protein hybrids.	Maltose	110-117	mesothelin	Homo sapiens	32-35
28225829-8	2017	With maltohexaose or amylopectin as substrates and using [UL-13C12]maltose in an isotopic dilution method, we discovered that BAM3 activity is inhibited by maltotriose at physiological (mM) concentrations, but not by maltose.	Maltose	67-74	Leucine-rich receptor-like protein kinase family protein	Arabidopsis thaliana	126-130
28152100-4	2017	Moreover, we show that leaves of CL grown mex1/pglct plants impaired in the chloroplastic maltose and glucose transporters display a severe dwarf phenotype and accumulate high levels of maltose, strongly indicating that the MEX1 and pGlcT transporters are involved in the export of starch breakdown products to the cytosol to support growth during illumination.	Maltose	90-97	root cap 1 (RCP1)	Arabidopsis thaliana	42-46
28152100-4	2017	Moreover, we show that leaves of CL grown mex1/pglct plants impaired in the chloroplastic maltose and glucose transporters display a severe dwarf phenotype and accumulate high levels of maltose, strongly indicating that the MEX1 and pGlcT transporters are involved in the export of starch breakdown products to the cytosol to support growth during illumination.	Maltose	90-97	plastidic GLC translocator	Arabidopsis thaliana	47-52
28152100-4	2017	Moreover, we show that leaves of CL grown mex1/pglct plants impaired in the chloroplastic maltose and glucose transporters display a severe dwarf phenotype and accumulate high levels of maltose, strongly indicating that the MEX1 and pGlcT transporters are involved in the export of starch breakdown products to the cytosol to support growth during illumination.	Maltose	90-97	root cap 1 (RCP1)	Arabidopsis thaliana	224-228
27714848-2	2017	Using fluorescent protein reporters we find that under non-inducing conditions the MAL32 promoter exhibits a low basal level of expression, similar to the GAL1 promoter, and that both promoters can be induced independently of each other using the respective sugars, maltose and galactose.	Maltose	266-273	alpha-glucosidase MAL32	Saccharomyces cerevisiae S288C	83-88
27871371-2	2017	Compared with the wild-type (WT) enzyme, the two truncated enzymes (DM1 and DM2) showed lower maltose- and trehalose-converting activities and a different transglycosylation reaction mechanism.	Maltose	94-101	immunoglobulin heavy diversity 1-7	Homo sapiens	68-71
27871371-2	2017	Compared with the wild-type (WT) enzyme, the two truncated enzymes (DM1 and DM2) showed lower maltose- and trehalose-converting activities and a different transglycosylation reaction mechanism.	Maltose	94-101	immunoglobulin heavy diversity 1-14 (non-functional)	Homo sapiens	76-79
27982108-5	2016	Human Tas1R2/Tas1R3 showed high sensitivity to sucrose, as expected; however, Japanese macaque Tas1R2/Tas1R3 showed equally high sensitivity to maltose and sucrose.	Maltose	144-151	taste 1 receptor member 2	Homo sapiens	95-101
27982108-5	2016	Human Tas1R2/Tas1R3 showed high sensitivity to sucrose, as expected; however, Japanese macaque Tas1R2/Tas1R3 showed equally high sensitivity to maltose and sucrose.	Maltose	144-151	taste 1 receptor member 3	Homo sapiens	102-108
27982108-7	2016	These results indicate that Japanese macaques have high sensitivity to maltose, and this sensitivity is directly related to Tas1R2/Tas1R3 function.	Maltose	71-78	taste 1 receptor member 2	Homo sapiens	124-130
27982108-7	2016	These results indicate that Japanese macaques have high sensitivity to maltose, and this sensitivity is directly related to Tas1R2/Tas1R3 function.	Maltose	71-78	taste 1 receptor member 3	Homo sapiens	131-137
27097641-5	2016	In this study, we presented that the lethal phenotype of the short-day sensitive cell death1 (sscd1) seedlings was suppressed by sugars including sucrose, glucose, fructose, and maltose in a dose-dependent manner.	Maltose	178-185	fumarylacetoacetase	Arabidopsis thaliana	94-99
27732676-3	2016	Here, we demonstrate that full-length RSK2-which is implicated in several types of cancer, and which is linked to the genetic Coffin-Lowry syndrome-can be overexpressed with high yields in Escherichia coli as a fusion with maltose binding protein (MBP), and can be purified to homogeneity after proteolytic removal of MBP by affinity and size-exclusion chromatography.	Maltose	223-230	ribosomal protein S6 kinase polypeptide 3	Mus musculus	38-42
27559824-5	2016	We have engineered a maltose binding protein fusion with Lin28, which binds let-7 miRNA with a Kd of 54.1 +- 4.2 nM, in agreement with previous data on a murine homologue.	Maltose	21-28	lin-28 homolog A	Mus musculus	57-62
27664470-6	2016	On the contrary, the control diet plus maltose binge caused lipid accumulation in Shp-/- mice, which was accompanied by a sharp elevation of CHOP, SREBP-1c, and REV-ERBalpha proteins but a diminished ATF4.	Maltose	39-46	nuclear receptor subfamily 0, group B, member 2	Mus musculus	82-85
27664470-6	2016	On the contrary, the control diet plus maltose binge caused lipid accumulation in Shp-/- mice, which was accompanied by a sharp elevation of CHOP, SREBP-1c, and REV-ERBalpha proteins but a diminished ATF4.	Maltose	39-46	DNA-damage inducible transcript 3	Mus musculus	141-145
27664470-6	2016	On the contrary, the control diet plus maltose binge caused lipid accumulation in Shp-/- mice, which was accompanied by a sharp elevation of CHOP, SREBP-1c, and REV-ERBalpha proteins but a diminished ATF4.	Maltose	39-46	sterol regulatory element binding transcription factor 1	Mus musculus	147-155
27664470-6	2016	On the contrary, the control diet plus maltose binge caused lipid accumulation in Shp-/- mice, which was accompanied by a sharp elevation of CHOP, SREBP-1c, and REV-ERBalpha proteins but a diminished ATF4.	Maltose	39-46	nuclear receptor subfamily 1, group D, member 1	Mus musculus	161-173
27664470-6	2016	On the contrary, the control diet plus maltose binge caused lipid accumulation in Shp-/- mice, which was accompanied by a sharp elevation of CHOP, SREBP-1c, and REV-ERBalpha proteins but a diminished ATF4.	Maltose	39-46	activating transcription factor 4	Mus musculus	200-204
27329414-4	2016	Furthermore, higher HSP12 expression level and more intracellular trehalose accumulation in yeast cells were observed by maltose supplementation with increase of the wort gravity from 18 P to 24 P, indicating higher stress response of yeast cells.	Maltose	121-128	lipid-binding protein HSP12	Saccharomyces cerevisiae S288C	20-25
26919272-7	2016	Substitution of Thr200 (corresponds to Val216 in S. cerevisiae isomaltase IMA1) with Val in MAL1 drastically reduced the hydrolysis of maltose-like substrates (alpha-1,4-glucosides), confirming the requirement of Thr at the respective position for this function.	Maltose	135-142	oligo-1,6-glucosidase IMA1	Saccharomyces cerevisiae S288C	74-78
27044345-1	2016	Pinto bean pod polysaccharide (PBPP) was successfully extracted with yield of 38.5g/100g and the PBPP gave total carbohydrate and uronic acid contents of 286.2mg maltose equivalent/g and 374.3mgGal/g, respectively.	Maltose	162-169	forkhead box L2	Homo sapiens	0-5
27328819-8	2016	mTOR-independent autophagy induction was also observed in HaCaT and HeLa cells treated with sucrose or raffinose but not in glucose, maltose or sorbitol treated HaCaT cells, indicating that autophagy induction was not a general property of saccharides.	Maltose	133-140	mechanistic target of rapamycin kinase	Homo sapiens	0-4
27231876-0	2016	Prokaryotic Soluble Overexpression and Purification of Human VEGF165 by Fusion to a Maltose Binding Protein Tag.	Maltose	84-91	long intergenic non-protein coding RNA 1194	Homo sapiens	108-111
27019682-2	2016	MBP is involved in maltose transport and bacterial chemotaxis; it binds to maltose and maltodextrins comprising alpha(1-4)-glucosidically linked linear glucose polymers and alpha(1-4)-glucosidically linked cyclodextrins.	Maltose	19-26	myelin basic protein	Homo sapiens	0-3
27011041-1	2016	During germination and early seedling growth of barley (Hordeum vulgare), maltase is responsible for the conversion of maltose produced by starch degradation in the endosperm to glucose for seedling growth.	Maltose	119-126	Agl1	Hordeum vulgare	74-81
27011041-4	2016	It has been proposed that maltase may be involved directly in starch granule degradation as well as in maltose hydrolysis.	Maltose	103-110	Agl1	Hordeum vulgare	26-33
27019682-2	2016	MBP is involved in maltose transport and bacterial chemotaxis; it binds to maltose and maltodextrins comprising alpha(1-4)-glucosidically linked linear glucose polymers and alpha(1-4)-glucosidically linked cyclodextrins.	Maltose	75-82	myelin basic protein	Homo sapiens	0-3
27019682-11	2016	Our mutant MBP retains maltose-binding activity and is suitable for reagentless fluorescence sensing.	Maltose	23-30	myelin basic protein	Homo sapiens	11-14
27463335-0	2016	Soluble Prokaryotic Expression and Purification of Human Interferon Alpha-2b Using a Maltose-Binding Protein Tag.	Maltose	85-92	interferon alpha 2	Homo sapiens	57-76
27487514-6	2016	Furthermore, glucose and maltose induced the highest postprandial glucose and insulin AUC values, whereas trehalose induced the lowest postprandial glucose and insulin AUC value amongst all carbohydrate sources, respectively, in obese cats.	Maltose	25-32	insulin	Felis catus	78-85
26498371-13	2015	Decrease of Na+/K+ ATPase and total ATPase enzymes activity was related with molecule size and number of maltose groups on the surface of molecule.	Maltose	105-112	dynein axonemal heavy chain 8	Homo sapiens	19-25
26498371-13	2015	Decrease of Na+/K+ ATPase and total ATPase enzymes activity was related with molecule size and number of maltose groups on the surface of molecule.	Maltose	105-112	dynein axonemal heavy chain 8	Homo sapiens	36-42
26625290-2	2015	Here, the crystallization and structure determination of a quaternary nuclear export complex consisting of the exportin CRM1, the small GTPase Ran in its GTP-bound form, the export cargo SPN1 and an FG repeat-containing fragment of the nuclear pore complex component nucleoporin Nup214 fused to maltose-binding protein is reported.	Maltose	295-302	exportin 1	Homo sapiens	120-124
26450977-0	2015	Correction for Du et al., Nasal Immunization with a Fusion Protein Consisting of the Hemagglutinin A Antigenic Region and the Maltose-Binding Protein Elicits CD11c+ CD8+ Dendritic Cells for Induced Long-Term Protective Immunity.	Maltose	126-133	integrin subunit alpha X	Homo sapiens	158-163
26411353-3	2015	In this study, six ginsenoside Rg1-alpha-glucosides were found to be synthesized from the reaction mixture of maltose as a donor and ginsenoside Rg1 as a sugar acceptor in the presence of rat small intestinal homogenates, which exhibit high alpha-glucosidase activities.	Maltose	110-117	protein phosphatase 1 regulatory subunit 3A	Homo sapiens	31-34
26450977-0	2015	Correction for Du et al., Nasal Immunization with a Fusion Protein Consisting of the Hemagglutinin A Antigenic Region and the Maltose-Binding Protein Elicits CD11c+ CD8+ Dendritic Cells for Induced Long-Term Protective Immunity.	Maltose	126-133	CD8a molecule	Homo sapiens	165-168
25804337-7	2015	The optimum combination of tag, expression temperature, co-expression of chaperones and host strain (His6-tag, 37 C, GroEL/GroES, E. coli BL21(DE3)) led to a 264-fold improvement of the volumetric epimerase activity, a measure of the soluble expression, compared to the starting conditions (His6-maltose-binding protein-tag, 20 C, without chaperones, E. coli BL21(DE3)).	Maltose	296-303	GroEL	Escherichia coli	117-122
26176916-4	2015	Two additional structures of GLUT3 bound to the exofacial inhibitor maltose were obtained at 2.6 A in the outward-open and 2.4 A in the outward-occluded states.	Maltose	68-75	solute carrier family 2 member 3	Homo sapiens	29-34
25301530-6	2015	The corresponding secondary chemical shifts suggest that the filamentous form of MAVS(CARD) retains an exclusively alpha-helical fold that is very similar to the X-ray structure determined previously from monomeric MAVS(CARD)-maltose binding protein fusion constructs.	Maltose	226-233	mitochondrial antiviral signaling protein	Homo sapiens	81-85
25301530-6	2015	The corresponding secondary chemical shifts suggest that the filamentous form of MAVS(CARD) retains an exclusively alpha-helical fold that is very similar to the X-ray structure determined previously from monomeric MAVS(CARD)-maltose binding protein fusion constructs.	Maltose	226-233	mitochondrial antiviral signaling protein	Homo sapiens	215-219
26121597-6	2015	When a single copy of this betaTCP-binding peptide sequence was fused to EGF via a flexible peptide tether domain and expressed recombinantly in E. coli together with a maltose-binding domain to aid purification, the resulting fusion protein exhibited modest affinity for betaTCP.	Maltose	169-176	epidermal growth factor	Homo sapiens	73-76
25843863-3	2015	alpha-Amylase adsorption to cellulose was reversible, attaining equilibrium within 30min of incubation, and showed a higher affinity at 37 C compared to 20 and 0 C. The adsorption was almost unchanged in the presence of maltose (2.5-20mM) but was hindered in the presence of excess protein, suggesting non-specific adsorption of alpha-amylase to cellulose.	Maltose	220-227	alpha-amylase	Zea mays	0-13
25601391-1	2015	Maltose-binding protein (MBP), a component of the maltose transport system of Escherichia coli, has been commonly thought to have minimal bioactivity.	Maltose	50-57	myelin basic protein	Mus musculus	25-28
25877163-3	2015	In this study, we focus on the effects of PGM2 (encoding for the phosphoglucomutase) and SNR84 (encoding for the H/ACA snoRNA) that are not directly related to both the maltose metabolic pathway and known regulatory networks of maltose metabolism on the leavening ability of baker"s yeast in lean dough.	Maltose	228-235	SNR84	Saccharomyces cerevisiae S288C	89-94
26073997-3	2015	In this study, we focus on the effects of regulators (GLC7 encoding the catalytic and REG1 encoding the regulatory subunits of protein phosphatase type 1) of glucose repression on maltose metabolism and leavening ability of baker"s yeast in lean dough.	Maltose	180-187	type 1 serine/threonine-protein phosphatase catalytic subunit GLC7	Saccharomyces cerevisiae S288C	54-58
26073997-3	2015	In this study, we focus on the effects of regulators (GLC7 encoding the catalytic and REG1 encoding the regulatory subunits of protein phosphatase type 1) of glucose repression on maltose metabolism and leavening ability of baker"s yeast in lean dough.	Maltose	180-187	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	86-90
26073997-5	2015	The results suggest that GLC7 and/or REG1 deletions increased maltose metabolism and leavening ability at different level with glucose derepression and increased enzymes (maltase and maltose permease) activities.	Maltose	62-69	type 1 serine/threonine-protein phosphatase catalytic subunit GLC7	Saccharomyces cerevisiae S288C	25-29
26073997-5	2015	The results suggest that GLC7 and/or REG1 deletions increased maltose metabolism and leavening ability at different level with glucose derepression and increased enzymes (maltase and maltose permease) activities.	Maltose	62-69	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	37-41
26073997-6	2015	In a medium containing glucose and maltose, at the point of glucose exhaustion the maltose metabolized and the leavening ability were increased 59.3% and 23.1%, respectively, in the case of a REG1 single gene deletion.	Maltose	35-42	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	192-196
26073997-6	2015	In a medium containing glucose and maltose, at the point of glucose exhaustion the maltose metabolized and the leavening ability were increased 59.3% and 23.1%, respectively, in the case of a REG1 single gene deletion.	Maltose	83-90	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	192-196
26073329-2	2015	METHODS: Codon-optimized cDNA of human 5-HT3A was inserted into a modified BacMam vector, which contained an IgG leader sequence, an 8xHis tag linked with two-Maltose Binding Proteins (MBP), and a TEV protease cleavage site.	Maltose	159-166	5-hydroxytryptamine receptor 3A	Homo sapiens	39-45
26026833-9	2015	In addition, maltose and l-alanine were found to increase the expression of pld gene.	Maltose	13-20	phospholipase D	Purpureocillium lilacinum	76-79
25804337-7	2015	The optimum combination of tag, expression temperature, co-expression of chaperones and host strain (His6-tag, 37 C, GroEL/GroES, E. coli BL21(DE3)) led to a 264-fold improvement of the volumetric epimerase activity, a measure of the soluble expression, compared to the starting conditions (His6-maltose-binding protein-tag, 20 C, without chaperones, E. coli BL21(DE3)).	Maltose	296-303	chaperonin GroES	Escherichia coli	123-128
25909780-1	2015	Crystallization of a maltose-binding protein MCL1 fusion has yielded a robust crystallography platform that generated the first apo MCL1 crystal structure, as well as five ligand-bound structures.	Maltose	21-28	MCL1 apoptosis regulator, BCL2 family member	Homo sapiens	45-49
25941931-0	2015	Escherichia coli Maltose-Binding Protein Induces M1 Polarity of RAW264.7 Macrophage Cells via a TLR2- and TLR4-Dependent Manner.	Maltose	17-24	toll-like receptor 2	Mus musculus	96-100
25941931-0	2015	Escherichia coli Maltose-Binding Protein Induces M1 Polarity of RAW264.7 Macrophage Cells via a TLR2- and TLR4-Dependent Manner.	Maltose	17-24	toll-like receptor 4	Mus musculus	106-110
25941931-1	2015	Maltose-binding protein (MBP) is a critical player of the maltose/maltodextrin transport system in Escherichia coli.	Maltose	58-65	myelin basic protein	Mus musculus	25-28
25909780-1	2015	Crystallization of a maltose-binding protein MCL1 fusion has yielded a robust crystallography platform that generated the first apo MCL1 crystal structure, as well as five ligand-bound structures.	Maltose	21-28	MCL1 apoptosis regulator, BCL2 family member	Homo sapiens	132-136
25837849-8	2015	The major facilitator superfamily of secondary active transporters is used to illustrate these ideas, which are then be expanded to primary active transport mediated by ABC (ATP-binding cassette) import systems, with a focus on the well-studied maltose transporter.	Maltose	245-252	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	169-172
25837849-8	2015	The major facilitator superfamily of secondary active transporters is used to illustrate these ideas, which are then be expanded to primary active transport mediated by ABC (ATP-binding cassette) import systems, with a focus on the well-studied maltose transporter.	Maltose	245-252	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	174-194
25248982-3	2015	In the present study, RANKL was expressed as a soluble maltose binding protein (MBP)-fusion protein using the Escherichia coli maltose binding domain tag system (pMAL) expression vector system.	Maltose	55-62	TNF superfamily member 11	Rattus norvegicus	22-27
25516912-6	2015	With the enzymatic hydrolysis of alpha-glucosidase, maltotriose and maltose can be turned into glucose rapidly, which can be quantitatively measured using a portable PGM.	Maltose	68-75	sucrase-isomaltase	Homo sapiens	33-50
25562209-2	2015	Limit dextrinase (LD) is the only endogenous barley enzyme capable of hydrolyzing the alpha-1,6-glucosidic bond during seed germination, and impaired LD activity inevitably reduces the maltose and glucose yields from starch degradation.	Maltose	185-192	LOC548116	Hordeum vulgare	0-16
25486965-4	2015	We found that GLP1 secretion induced by miglitol plus maltose was significantly higher than that by another alpha-GI, acarbose, plus maltose, despite the fact that acarbose inhibits maltase more potently than miglitol.	Maltose	54-61	glucagon	Homo sapiens	14-18
25486965-8	2015	Single administration of miglitol triggered no GLP1 secretion, and GLP1 secretion by miglitol plus maltose was significantly attenuated by atropine pretreatment, suggesting regulation via vagal nerve.	Maltose	99-106	glucagon	Homo sapiens	67-71
25248982-7	2015	Dialysis was then carried out to remove binding maltose from the cleaved rRANKL solution.	Maltose	48-55	TNF superfamily member 11	Rattus norvegicus	73-79
24999995-1	2014	We have previously shown that a genetically encoded bioluminescent resonance energy transfer (BRET) biosensor, comprising maltose binding protein (MBP) flanked by a green fluorescent protein (GFP(2)) at the N-terminus and a variant of Renilla luciferase (RLuc2) at the C-terminus, has superior sensitivity and limits of detection for maltose, compared with an equivalent fluorescent resonance energy transfer (FRET) biosensor.	Maltose	122-129	myelin basic protein	Homo sapiens	147-150
26656820-7	2015	Since maltose cannot render the mixture blue as strongly as glucose, the present method has been successfully applied to a microtiter plate assay of alpha-glucosidase with the disaccharide.	Maltose	6-13	sucrase-isomaltase	Homo sapiens	149-166
24999995-2	2014	Here, we demonstrate that the same MBP biosensor can be combined with a microfluidic system for detection of maltose in water or beer.	Maltose	109-116	myelin basic protein	Homo sapiens	35-38
24971648-6	2014	Now we have determined the disulfide linkages in soluble and biologically active recombinant maltose binding protein-HBx fusion protein using matrix-assisted laser desorption ionization time-of-flight mass spectrometry.	Maltose	93-100	X protein	Hepatitis B virus	117-120
24099511-4	2014	RESULTS: SLN could be freeze-dried using 10% sucrose, trehalose or maltose.	Maltose	67-74	sarcolipin	Homo sapiens	9-12
25220864-6	2014	Here, we describe an efficient system for expressing and purifying active and stable TMLH as a maltose-binding protein fusion in Escherichiacoli.	Maltose	95-102	trimethyllysine hydroxylase, epsilon	Homo sapiens	85-89
24993311-5	2014	RESULTS: Results strongly suggest that the deletion of MIG1 and/or TUP1 and/or SSN6 can exert various effects on glucose repression for maltose metabolism.	Maltose	136-143	transcription factor MIG1	Saccharomyces cerevisiae S288C	55-59
24993311-5	2014	RESULTS: Results strongly suggest that the deletion of MIG1 and/or TUP1 and/or SSN6 can exert various effects on glucose repression for maltose metabolism.	Maltose	136-143	chromatin-silencing transcriptional regulator TUP1	Saccharomyces cerevisiae S288C	67-71
24993311-5	2014	RESULTS: Results strongly suggest that the deletion of MIG1 and/or TUP1 and/or SSN6 can exert various effects on glucose repression for maltose metabolism.	Maltose	136-143	transcription regulator CYC8	Saccharomyces cerevisiae S288C	79-83
24993311-6	2014	The deletion of TUP1 was negative for glucose derepression to facilitate the maltose metabolism.	Maltose	77-84	chromatin-silencing transcriptional regulator TUP1	Saccharomyces cerevisiae S288C	16-20
24993311-7	2014	By contrast, the deletion of MIG1 and/or SSN6, rather than other double-gene or triple-gene mutations could partly relieve glucose repression, thereby promoting maltose metabolism and the leavening ability of baker"s yeast in lean dough.	Maltose	161-168	transcription factor MIG1	Saccharomyces cerevisiae S288C	29-33
24993311-7	2014	By contrast, the deletion of MIG1 and/or SSN6, rather than other double-gene or triple-gene mutations could partly relieve glucose repression, thereby promoting maltose metabolism and the leavening ability of baker"s yeast in lean dough.	Maltose	161-168	transcription regulator CYC8	Saccharomyces cerevisiae S288C	41-45
24825603-0	2014	Escherichia coli maltose-binding protein activates mouse peritoneal macrophages and induces M1 polarization via TLR2/4 in vivo and in vitro.	Maltose	17-24	toll-like receptor 2	Mus musculus	112-118
24825603-1	2014	Maltose-binding protein (MBP) is a component of the maltose transport system of Escherichia coli.	Maltose	52-59	myelin basic protein	Mus musculus	25-28
24865334-5	2014	Here, we describe a method by which recombinant human Pen-2 can be purified from bacteria to > 95% purity at milligram quantities per liter, utilizing a maltose binding protein tag to both increase solubility and facilitate purification.	Maltose	156-163	presenilin enhancer, gamma-secretase subunit	Homo sapiens	54-59
24865334-6	2014	Expressing the same construct in mammalian cells, we show that the large N-terminal maltose binding protein tag on Pen-2 still permits incorporation into the complex and subsequent presenilin-1 endoproteolysis, nicastrin glycosylation and proteolytic activity.	Maltose	84-91	presenilin enhancer, gamma-secretase subunit	Homo sapiens	115-120
24865334-6	2014	Expressing the same construct in mammalian cells, we show that the large N-terminal maltose binding protein tag on Pen-2 still permits incorporation into the complex and subsequent presenilin-1 endoproteolysis, nicastrin glycosylation and proteolytic activity.	Maltose	84-91	presenilin 1	Homo sapiens	181-193
25152391-3	2014	In this study, crystal structure of the GH1 domain of GKAP from Rattus norvegicus was determined in fusion with an N-terminal maltose-binding protein at 2.0 A resolution.	Maltose	126-133	DLG associated protein 1	Rattus norvegicus	54-58
24920206-8	2014	Deletion of acetyltransferase SAS2 enhances this phenotype and maltose fermentation even more.	Maltose	63-70	histone acetyltransferase	Saccharomyces cerevisiae S288C	30-34
24837693-5	2014	Cyclic voltammetric studies showed enhanced redox properties for Pd-Ni/CNF-based electrodes relative to the Ni-metal electrode and significantly improved electrocatalytic activity for sugar (e.g., glucose, fructose, sucrose, and maltose) oxidation.	Maltose	229-236	NPHS1 adhesion molecule, nephrin	Homo sapiens	71-74
24835094-2	2014	Maltose-forming alpha-amylase is a glycoside hydrolase family 57 (GH57) member that is unique because it displays dual hydrolysis activity toward alpha-1,4- and alpha-1,6-glycosidic linkages and only recognizes maltose.	Maltose	211-218	alpha-amylase family glycosyl hydrolase	Thermococcus cleftensis	16-29
24835094-2	2014	Maltose-forming alpha-amylase is a glycoside hydrolase family 57 (GH57) member that is unique because it displays dual hydrolysis activity toward alpha-1,4- and alpha-1,6-glycosidic linkages and only recognizes maltose.	Maltose	211-218	glycoside hydrolase family 57	Thermococcus cleftensis	35-64
24835094-2	2014	Maltose-forming alpha-amylase is a glycoside hydrolase family 57 (GH57) member that is unique because it displays dual hydrolysis activity toward alpha-1,4- and alpha-1,6-glycosidic linkages and only recognizes maltose.	Maltose	211-218	glycoside hydrolase family 57	Thermococcus cleftensis	66-70
24835094-6	2014	To characterize the subgroup B maltose-forming alpha-amylase from Thermococcus species (TCMA), we cloned the CL1_0868 gene from Thermococcus sp.	Maltose	31-38	alpha-amylase family glycosyl hydrolase	Thermococcus cleftensis	47-60
24835094-6	2014	To characterize the subgroup B maltose-forming alpha-amylase from Thermococcus species (TCMA), we cloned the CL1_0868 gene from Thermococcus sp.	Maltose	31-38	glycoside hydrolase	Thermococcus cleftensis	109-117
24131788-0	2014	The high-affinity maltose switch MBP317-347 has low affinity for glucose: implications for targeting tumors with metabolically directed enzyme prodrug therapy.	Maltose	18-25	myelin basic protein	Homo sapiens	33-36
25035870-0	2014	Three Agt1 transporters from brewer"s yeasts exhibit different temperature dependencies for maltose transport over the range of brewery temperatures (0-20  C).	Maltose	92-99	alpha-glucoside permease	Saccharomyces cerevisiae S288C	6-10
24131788-3	2014	A molecular switch, MBP317-347, originally designed to be a high-affinity switch for maltose and maltose-like polysaccharides, was demonstrated to be a low-affinity switch for glucose, that is, able to be activated by high concentrations (tens of millimolar) of glucose.	Maltose	85-92	myelin basic protein	Homo sapiens	20-23
24131788-3	2014	A molecular switch, MBP317-347, originally designed to be a high-affinity switch for maltose and maltose-like polysaccharides, was demonstrated to be a low-affinity switch for glucose, that is, able to be activated by high concentrations (tens of millimolar) of glucose.	Maltose	97-104	myelin basic protein	Homo sapiens	20-23
23998289-4	2014	The docking and screening from TCM database results indicate the vitamin B2, 3 beta-isodihydrocadambine, and caribine display higher binding affinity than maltose in maltose binding protein (MBP).	Maltose	155-162	myelin basic protein	Homo sapiens	166-189
24649402-10	2014	We finally found a mixed inhibition by maltose for Ima5p while, contrary to a previous work, Ima1p inhibition by maltose was competitive at very low isomaltose concentrations and uncompetitive as the substrate concentration increased.	Maltose	39-46	oligo-1,6-glucosidase IMA5	Saccharomyces cerevisiae S288C	51-56
24649402-10	2014	We finally found a mixed inhibition by maltose for Ima5p while, contrary to a previous work, Ima1p inhibition by maltose was competitive at very low isomaltose concentrations and uncompetitive as the substrate concentration increased.	Maltose	113-120	oligo-1,6-glucosidase IMA1	Saccharomyces cerevisiae S288C	93-98
24271181-1	2014	In this study, the regulator MalR (Saci_1161) of the TrmB family from Sulfolobus acidocaldarius was identified and was shown to be involved in transcriptional control of the maltose regulon (Saci_1660 to Saci_1666), including the ABC transporter (malEFGK), alpha-amylase (amyA), and alpha-glycosidase (malA).	Maltose	174-181	ATZ20_RS03540	Sulfolobus acidocaldarius	257-270
24271181-1	2014	In this study, the regulator MalR (Saci_1161) of the TrmB family from Sulfolobus acidocaldarius was identified and was shown to be involved in transcriptional control of the maltose regulon (Saci_1660 to Saci_1666), including the ABC transporter (malEFGK), alpha-amylase (amyA), and alpha-glycosidase (malA).	Maltose	174-181	ATZ20_RS03540	Sulfolobus acidocaldarius	272-276
24070540-6	2014	In this review we summarize some recent developments in the use of paramagnetic relaxation enhancement to directly study sparsely-populated states of proteins and illustrate the application of this approach to two proteins, maltose binding protein and calmodulin, both of which undergo large rigid body conformational rearrangements upon ligand binding from an open apo state to a closed ligand-bound holo state.	Maltose	224-231	calmodulin 1	Homo sapiens	252-262
23998289-4	2014	The docking and screening from TCM database results indicate the vitamin B2, 3 beta-isodihydrocadambine, and caribine display higher binding affinity than maltose in maltose binding protein (MBP).	Maltose	155-162	myelin basic protein	Homo sapiens	191-194
24111992-9	2013	Met(11) or Thr(11) SP-D in serum from transgenic mice bound maltose in a calcium-dependent manner, and binding was inhibited in the presence of EDTA or maltose.	Maltose	60-67	surfactant associated protein D	Mus musculus	19-23
25984594-9	2014	In contrast to these claims, we find that sweet GRNs of Gr64a homozygous mutant flies show normal responses to most sugars, and only modestly reduced responses to maltose and maltotriose.	Maltose	163-170	Gustatory receptor 64a	Drosophila melanogaster	56-61
25711084-2	2014	The alteration of SGLT1 and GLUT2 transporter distribution in absorptive cell of intestine villus depending on maltose concentration has been determined using the confocal microscope.	Maltose	111-118	solute carrier family 5 member 1	Homo sapiens	18-23
25711084-2	2014	The alteration of SGLT1 and GLUT2 transporter distribution in absorptive cell of intestine villus depending on maltose concentration has been determined using the confocal microscope.	Maltose	111-118	solute carrier family 2 member 2	Homo sapiens	28-33
24111992-9	2013	Met(11) or Thr(11) SP-D in serum from transgenic mice bound maltose in a calcium-dependent manner, and binding was inhibited in the presence of EDTA or maltose.	Maltose	152-159	surfactant associated protein D	Mus musculus	19-23
24223944-3	2013	We therefore investigated whether the elevated maltose level in mex1-1 in the warm could result in changes in metabolism and physiology typical of WT plants grown in the cold.	Maltose	47-54	root cap 1 (RCP1)	Arabidopsis thaliana	64-68
23950181-2	2013	The conversion involves the cytosolic metabolism of maltose to hexose phosphates via an unusual, multidomain protein with 4-glucanotransferase activity, DPE2, believed to transfer glucosyl moieties to a complex heteroglycan prior to their conversion to hexose phosphate via a cytosolic phosphorylase.	Maltose	52-59	disproportionating enzyme 2	Arabidopsis thaliana	153-157
23263832-4	2013	The results showed that the hot-water extract of the leaves significantly suppressed the increase of blood glucose levels after glucose, maltose and starch loading.	Maltose	137-144	alcohol dehydrogenase, iron containing, 1	Mus musculus	28-31
23506949-2	2013	Dendrimers have been proposed as new carriers to ameliorate DC antigen loading and in this way, we have determined the potential use of maltose decorated neutrally and positively charged G4 glycodendrimers.	Maltose	136-143	chemokine (C-C motif) ligand 22	Mus musculus	60-62
23506949-7	2013	This is the first study for exploring the use of maltose-functionalized dendrimers-peptides complexes as a potential DC-based vaccine candidate.	Maltose	49-56	chemokine (C-C motif) ligand 22	Mus musculus	117-119
23506949-8	2013	FROM THE CLINICAL EDITOR: In this paper, maltose-functionalized dendrimer-peptide complexes are demonstrated to activate the immune system by way of dendritic cell (DC) stimulation.	Maltose	41-48	chemokine (C-C motif) ligand 22	Mus musculus	165-167
24086489-4	2013	When expressed in Escherichia coli as a recombinant protein with a maltose binding protein tag, UGT73C14 displayed enzymatic activity toward ABA and utilized UDP-glucose and UDP-galactose as the sugar donors.	Maltose	67-74	UDP-glycosyltransferase 73C6-like	Gossypium hirsutum	96-104
24688719-5	2013	The biotechnological protocols include expression of the recombinant CB2 in E. coli cells as a fusion with the maltose binding protein, stabilization with a high affinity ligand and a derivative of cholesterol in detergent micelles, efficient purification by tandem affinity chromatography, and reconstitution of the receptor into lipid bilayers.	Maltose	111-118	cannabinoid receptor 2	Homo sapiens	69-72
24161396-5	2013	A maltose-binding protein pull-down assay demonstrated that Klf4 binds to the Zfp296 158-483 amino acid region, and that Zfp296 binds to the Klf4 DNA-binding domain (DBD).	Maltose	2-9	Kruppel-like factor 4 (gut)	Mus musculus	60-64
23415925-6	2013	The purified N-terminal Tm-1 fragment from which the maltose-binding protein tag had been removed has inhibitory activity against ToMV RNA replication.	Maltose	53-60	toMV resistance protein Tm-1(GCR237)	Solanum lycopersicum	24-28
22651799-4	2013	Therefore, OXA-23 was fused to maltose-binding protein of Escherichia coli, the fused protein was expressed and purified to homogeneity.	Maltose	31-38	class D beta-lactamase OXA-23	Acinetobacter baumannii	11-17
23596054-0	2013	Interaction of wheat beta-amylase with maltose and glucose as examined by fluorescence.	Maltose	39-46	beta-amylase	Triticum aestivum	21-33
23596054-1	2013	Fluorescence of wheat beta-amylase (WBA) was quenched by the interaction with maltose or glucose, which are competitive inhibitors of WBA, suggesting that the states of tryptophan and tyrosine residues could be changed by the interaction.	Maltose	78-85	beta-amylase	Triticum aestivum	22-34
23508996-3	2013	Here we report a 2.0 A crystal structure of the human NLRP1 CARD as a fusion with the maltose-binding protein.	Maltose	86-93	NLR family pyrin domain containing 1	Homo sapiens	54-59
23721409-2	2013	When a small label was incorporated on the cytosolic interface of transmembrane helix 6 (Cys-265), (19)F NMR spectra of the beta2 adrenergic receptor (beta2AR) reconstituted in maltose/neopentyl glycol detergent micelles revealed two distinct inactive states, an activation intermediate state en route to activation, and, in the presence of a G protein mimic, a predominant active state.	Maltose	177-184	adrenoceptor beta 2	Homo sapiens	124-149
23721409-2	2013	When a small label was incorporated on the cytosolic interface of transmembrane helix 6 (Cys-265), (19)F NMR spectra of the beta2 adrenergic receptor (beta2AR) reconstituted in maltose/neopentyl glycol detergent micelles revealed two distinct inactive states, an activation intermediate state en route to activation, and, in the presence of a G protein mimic, a predominant active state.	Maltose	177-184	adrenoceptor beta 2	Homo sapiens	151-158
23390139-6	2013	SP-D lectin activity was also tested towards maltose-agarose and mannan for selected BALF samples.	Maltose	45-52	surfactant protein D	Homo sapiens	0-4
23400970-3	2013	We have previously demonstrated that the nonhomologous recombination of the genes encoding maltose binding protein (MBP) and TEM1 beta-lactamase (BLA) can result in genes that confer maltose-dependent resistance to beta-lactam antibiotics even though the encoded proteins are not allosteric enzymes.	Maltose	91-98	myelin basic protein	Homo sapiens	116-119
22794932-4	2013	The sensitivity at 0.700V was (1.94+-0.03) mAM(-1) (r=0.9991), with a linear range between 0.25 and 5.00mM, a detection limit of 2.2muM and a quantification limit of 6.7muM with minimum interference from lactose (1.5%), maltose (5.7%), galactose (1.2%), ascorbic acid (1.0%), and uric acid (3.3%).	Maltose	220-227	mastermind like transcriptional coactivator 1	Mus musculus	43-49
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	67-74	bicoid	Drosophila melanogaster	59-62
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	67-74	bicoid	Drosophila melanogaster	157-160
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	67-74	bicoid	Drosophila melanogaster	157-160
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	67-74	bicoid	Drosophila melanogaster	157-160
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	67-74	bicoid	Drosophila melanogaster	157-160
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	161-168	bicoid	Drosophila melanogaster	59-62
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	161-168	bicoid	Drosophila melanogaster	157-160
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	161-168	bicoid	Drosophila melanogaster	157-160
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	161-168	bicoid	Drosophila melanogaster	157-160
23083905-5	2013	The half maximal effective concentration (EC(50)) was 0.37 muM for maltose and the response was linear over almost three log units ranging from 10nM to 3.16 muM maltose for the BRET(2) system compared to an EC(50) of 2.3 muM and a linear response ranging from 0.3 muM to 21.1 muM for the equivalent FRET-based biosensor.	Maltose	161-168	bicoid	Drosophila melanogaster	157-160
23411612-0	2013	Periplasmic binding protein-based detection of maltose using liposomes: a new class of biorecognition elements in competitive assays.	Maltose	47-54	phosphatidylethanolamine binding protein 1	Homo sapiens	0-27
23411612-6	2013	MBP conjugated fluorescent dye-encapsulating liposomes served to provide recognition and signal amplification in a competitive assay for maltose using amylose magnetic beads in a microtiter plate-based format.	Maltose	137-144	myelin basic protein	Homo sapiens	0-3
22933379-0	2013	How maltose influences structural changes to bind to maltose-binding protein: results from umbrella sampling simulation.	Maltose	4-11	myelin basic protein	Homo sapiens	53-76
22933379-1	2013	A well-studied periplasmic-binding protein involved in the abstraction of maltose is maltose-binding protein (MBP), which undergoes a ligand-induced conformational transition from an open (ligand-free) to a closed (ligand-bound) state.	Maltose	74-81	myelin basic protein	Homo sapiens	85-108
22933379-1	2013	A well-studied periplasmic-binding protein involved in the abstraction of maltose is maltose-binding protein (MBP), which undergoes a ligand-induced conformational transition from an open (ligand-free) to a closed (ligand-bound) state.	Maltose	74-81	myelin basic protein	Homo sapiens	110-113
22933379-2	2013	Umbrella sampling simulations have been us to estimate the free energy of binding of maltose to MBP and to trace the potential of mean force of the unbinding event using the center-of-mass distance between the protein and ligand as the reaction coordinate.	Maltose	85-92	myelin basic protein	Homo sapiens	96-99
24025570-3	2013	The maltose binding protein-fused heavy chain variable region (MBP-V(H)) of an antibody that recognizes the C-terminal fragment of human osteocalcin (bone Gla protein, BGP), a biomarker for bone-related diseases, was immobilized onto microplate wells, and the antigen together with streptavidin (SA)-fused light chain variable region of the same antibody (SA-V(L)) was added and incubated.	Maltose	4-11	myelin basic protein	Homo sapiens	63-66
24025570-3	2013	The maltose binding protein-fused heavy chain variable region (MBP-V(H)) of an antibody that recognizes the C-terminal fragment of human osteocalcin (bone Gla protein, BGP), a biomarker for bone-related diseases, was immobilized onto microplate wells, and the antigen together with streptavidin (SA)-fused light chain variable region of the same antibody (SA-V(L)) was added and incubated.	Maltose	4-11	bone gamma-carboxyglutamate protein	Homo sapiens	137-148
24025570-3	2013	The maltose binding protein-fused heavy chain variable region (MBP-V(H)) of an antibody that recognizes the C-terminal fragment of human osteocalcin (bone Gla protein, BGP), a biomarker for bone-related diseases, was immobilized onto microplate wells, and the antigen together with streptavidin (SA)-fused light chain variable region of the same antibody (SA-V(L)) was added and incubated.	Maltose	4-11	bone gamma-carboxyglutamate protein	Homo sapiens	168-171
23036359-10	2012	Enzymatic kinetics revealed these enzymes both preferentially cleave the alpha1-6 linkage in comparison to the expected alpha1-4 and specifically favor maltose-derived substrates of longer length.	Maltose	152-159	adrenoceptor alpha 1D	Homo sapiens	73-81
23220582-4	2013	Expression of the parasite GAD genes and the corresponding Drosophila melanogaster (fruit fly) GAD1 as well as the mouse GAD(65) and GAD(67) genes in Escherichia coli as maltose binding protein fusions resulted in functional enzymes in quantities compatible with the needs of high throughput inhibitor screening (HTS).	Maltose	170-177	Glutamic acid decarboxylase 1	Drosophila melanogaster	27-30
23220582-4	2013	Expression of the parasite GAD genes and the corresponding Drosophila melanogaster (fruit fly) GAD1 as well as the mouse GAD(65) and GAD(67) genes in Escherichia coli as maltose binding protein fusions resulted in functional enzymes in quantities compatible with the needs of high throughput inhibitor screening (HTS).	Maltose	170-177	glutamic acid decarboxylase 2	Mus musculus	121-128
22800814-4	2013	The PE impregnated with alpha-amylase (4 mug per 1mg PE) was used for hydrolyzing soluble potato starch to maltose.	Maltose	107-114	alpha-amylase	Solanum tuberosum	24-37
23036359-10	2012	Enzymatic kinetics revealed these enzymes both preferentially cleave the alpha1-6 linkage in comparison to the expected alpha1-4 and specifically favor maltose-derived substrates of longer length.	Maltose	152-159	adrenoceptor alpha 1D	Homo sapiens	120-128
23046344-2	2012	The maltose binding protein (MBP), a protein that belongs to the maltose transport system, has a structure composed of two globular domains separated by a rigid-body "hinge bending".	Maltose	4-11	myelin basic protein	Homo sapiens	29-32
22963794-4	2012	Consequently, we have developed an over-expression strategy that exploits the maltose binding protein as a fusion partner to stabilize and solubilize SelK.	Maltose	78-85	selenoprotein K	Homo sapiens	150-154
22924857-4	2012	By monitoring the same nanoparticles under various conditions, a single charge-transfer-based biosensor construct (one maltose binding protein, one protein attachment position for the reductant, one type of nanoparticle) showed a dynamic range for analyte (maltose) detection spanning from 100 pM to 10 muM while the emission intensities increase from 25 to 175% at the single-particle level.	Maltose	119-126	latexin	Homo sapiens	303-306
22924857-4	2012	By monitoring the same nanoparticles under various conditions, a single charge-transfer-based biosensor construct (one maltose binding protein, one protein attachment position for the reductant, one type of nanoparticle) showed a dynamic range for analyte (maltose) detection spanning from 100 pM to 10 muM while the emission intensities increase from 25 to 175% at the single-particle level.	Maltose	257-264	latexin	Homo sapiens	303-306
22820007-6	2012	The reproducibility of the DNP results is tested on the water soluble maltose binding protein MalE of the ABC maltose importer, where we determine a net standard deviation of 9% in the primary DNP data in the concentration range between 10 and 100 muM.	Maltose	70-77	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	106-109
22795862-1	2012	2-Deoxy-2-fluoro-d-glucose, 3-deoxy-3-fluoro-D-glucose and 6-deoxy-6-fluoro-D-glucose were converted into the corresponding maltose derivatives using Arabidopsis thaliana DPE2-mediated trans-glycosylation reaction with glycogen acting as a glucosyl donor.	Maltose	124-131	disproportionating enzyme 2	Arabidopsis thaliana	171-175
22820007-6	2012	The reproducibility of the DNP results is tested on the water soluble maltose binding protein MalE of the ABC maltose importer, where we determine a net standard deviation of 9% in the primary DNP data in the concentration range between 10 and 100 muM.	Maltose	110-117	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	106-109
22488179-2	2012	In vivo proton coupling of two previously reported Pma1p isoforms (Ser800Ala, Glu803Gln) with increased in vitro H(+)/ATP stoichiometries was analysed by measuring biomass yields of anaerobic maltose-limited chemostat cultures expressing only the different PMA1 alleles.	Maltose	192-199	H(+)-exporting P2-type ATPase PMA1	Saccharomyces cerevisiae S288C	51-56
22466447-4	2012	The study on the function of FLO10 (spsc) by its integrative expression in the non-flocculating industrial yeast indicated severe inhibition in the flocculation of the transformant by mannose and maltose, moderate inhibition by sucrose and glucose and no inhibition by xylose and galactose, and thus the NewFlo type was established.	Maltose	196-203	Flo10p	Saccharomyces cerevisiae S288C	29-34
22325262-2	2012	Using molecular simulations, we predicted that the binding interface between DARPin off7 and its ligand (maltose binding protein; MBP) is characterized by a hot-spot motif in which binding energy is largely concentrated on a few amino acids.	Maltose	105-112	myelin basic protein	Homo sapiens	130-133
22098298-7	2012	Compared to control plants, the adg1/APS1(C81S)  lines had higher levels of ADP-glucose and maltose, and either increased rates of starch synthesis or a starch-excess phenotype, depending on the daylength.	Maltose	92-99	ADP glucose pyrophosphorylase 1	Arabidopsis thaliana	32-36
22098298-7	2012	Compared to control plants, the adg1/APS1(C81S)  lines had higher levels of ADP-glucose and maltose, and either increased rates of starch synthesis or a starch-excess phenotype, depending on the daylength.	Maltose	92-99	ATP sulfurylase 1	Arabidopsis thaliana	37-41
23814438-4	2012	The present work describes an easy method of expression, purification and functional characterization in Escherichia coli of maize cystatin as a part of maltose-binding fusion protein.	Maltose	153-160	LOC100857070	Zea mays	131-139
22475504-9	2012	It is shown that glucose 6-phosphate isomerase and plastidial glucose 6-phosphate transport reactions are not at equilibrium, and light is shed on the pathways leading to fructose, maltose, and inositol synthesis.	Maltose	181-188	glucose-6-phosphate isomerase, cytosolic	Brassica napus	17-46
22266355-5	2012	Recombinant mouse and human FMO5 (mFMO5 and hFMO5, respectively) were expressed as maltose-binding fusion proteins from Escherichia coli, purified with affinity chromatography, and examined for their N-oxygenation functional activity at different pH values.	Maltose	83-90	flavin containing dimethylaniline monoxygenase 5	Homo sapiens	28-32
21866443-1	2011	Glucose, maltose, and mannose as sole carbon sources, induced synthesis of glucose dehydrogenase (GDH) in three strains of Pantoea with specific activities from 0.14 to 0.6 U/mg proteins.	Maltose	9-16	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	Homo sapiens	98-101
22509216-2	2012	This approach uses 2-F-labeled maltose as a spy ligand to indirectly probe protein-ligand or protein-protein interactions of proteins fused or tagged to the maltose-binding protein (MBP).	Maltose	31-38	myelin basic protein	Homo sapiens	157-180
22509216-2	2012	This approach uses 2-F-labeled maltose as a spy ligand to indirectly probe protein-ligand or protein-protein interactions of proteins fused or tagged to the maltose-binding protein (MBP).	Maltose	31-38	myelin basic protein	Homo sapiens	182-185
22509216-3	2012	The key feature is the simultaneous NMR observation of both (19)F NMR signals of gluco/manno-type-2-F-maltose-isomers; one isomer (alpha-gluco-type) binds to MBP and senses the protein interaction, and the nonbinding isomers (beta-gluco- and/or alpha/beta-manno-type) are utilized as internal references.	Maltose	102-109	myelin basic protein	Homo sapiens	158-161
22720063-10	2012	Mutagenesis and molecular modeling of an intact TEM-1 domain near MBP within the RG13 framework indicated a close surface proximity of the two domains with maltose switching being critically dependent on MBP linker anchoring residues and linker length.	Maltose	156-163	CD248 molecule	Homo sapiens	48-53
22720063-10	2012	Mutagenesis and molecular modeling of an intact TEM-1 domain near MBP within the RG13 framework indicated a close surface proximity of the two domains with maltose switching being critically dependent on MBP linker anchoring residues and linker length.	Maltose	156-163	myelin basic protein	Homo sapiens	66-69
22720063-10	2012	Mutagenesis and molecular modeling of an intact TEM-1 domain near MBP within the RG13 framework indicated a close surface proximity of the two domains with maltose switching being critically dependent on MBP linker anchoring residues and linker length.	Maltose	156-163	myelin basic protein	Homo sapiens	204-207
22720063-11	2012	Structural analysis indicated that the linker attachment sites on MBP are at a site that, upon maltose binding, harbors both the largest local Calpha distance changes and displays surface curvature changes, from concave to relatively flat becoming thus less sterically intrusive.	Maltose	95-102	myelin basic protein	Homo sapiens	66-69
22720063-12	2012	Maltose activation and zinc inhibition of RG13 are hypothesized to have opposite effects on productive relaxation of the TEM-1 beta3 linker region via steric and/or linker juxtapositioning mechanisms.	Maltose	0-7	CD248 molecule	Homo sapiens	121-126
22127878-1	2011	The synthesis and glucosidase inhibitory activities of two C-3"- and C-5"-beta-maltose-extended analogues of the naturally occurring sulfonium-ion inhibitor, de-O-sulfonated ponkoranol, are described.	Maltose	78-86	complement C5	Homo sapiens	69-72
22098354-4	2011	We review a selected set of simulation studies on ligand-induced changes in the chaperonin GroEL-GroES, a molecular folding machine, maltose-binding protein, a prototypical member of the periplasmic binding proteins, and the bacterial ribosomal A-site, focusing on aminoglycoside antibiotic recognition.	Maltose	133-140	heat shock protein family D (Hsp60) member 1	Homo sapiens	91-96
21968188-6	2011	Maltose binding protein pull-down and yeast two-hybrid indicated that SIRT1 bound to CKIIbeta, but not to CKIIalpha.	Maltose	0-7	sirtuin 1	Homo sapiens	70-75
21968188-6	2011	Maltose binding protein pull-down and yeast two-hybrid indicated that SIRT1 bound to CKIIbeta, but not to CKIIalpha.	Maltose	0-7	casein kinase 2 beta	Homo sapiens	85-93
21755532-2	2011	It has been shown that on maltose the expression level of AGT1 is much higher in ale strains than in lager strains, and that glucose represses the expression, particularly in the ale strains.	Maltose	26-33	alpha-glucoside permease	Saccharomyces cerevisiae S288C	58-62
21728233-3	2011	For the AG-GOx assay, maltose is used as AG substrate and hydrolyzed to glucose which is then oxidized by the GOx activity.	Maltose	22-29	hydroxyacid oxidase 1	Homo sapiens	11-14
21728233-3	2011	For the AG-GOx assay, maltose is used as AG substrate and hydrolyzed to glucose which is then oxidized by the GOx activity.	Maltose	22-29	hydroxyacid oxidase 1	Homo sapiens	110-113
21728233-4	2011	It is shown that the PSU-Py membrane acts as a fluorescence indicator of the enzymatic reactions, and both GOx and AG/GOx enzyme assays are successfully applied for glucose, maltose and acorbose analysis in the range 0.125-2.0 x 10(-3) M glucose, 0.05-0.5 x 10(-3) M maltose, and 0.0125-0.1 mg   mL(-1) acorbose, respectively.	Maltose	174-181	hydroxyacid oxidase 1	Homo sapiens	107-110
21728233-4	2011	It is shown that the PSU-Py membrane acts as a fluorescence indicator of the enzymatic reactions, and both GOx and AG/GOx enzyme assays are successfully applied for glucose, maltose and acorbose analysis in the range 0.125-2.0 x 10(-3) M glucose, 0.05-0.5 x 10(-3) M maltose, and 0.0125-0.1 mg   mL(-1) acorbose, respectively.	Maltose	174-181	hydroxyacid oxidase 1	Homo sapiens	118-121
21728233-4	2011	It is shown that the PSU-Py membrane acts as a fluorescence indicator of the enzymatic reactions, and both GOx and AG/GOx enzyme assays are successfully applied for glucose, maltose and acorbose analysis in the range 0.125-2.0 x 10(-3) M glucose, 0.05-0.5 x 10(-3) M maltose, and 0.0125-0.1 mg   mL(-1) acorbose, respectively.	Maltose	267-274	hydroxyacid oxidase 1	Homo sapiens	107-110
21728233-4	2011	It is shown that the PSU-Py membrane acts as a fluorescence indicator of the enzymatic reactions, and both GOx and AG/GOx enzyme assays are successfully applied for glucose, maltose and acorbose analysis in the range 0.125-2.0 x 10(-3) M glucose, 0.05-0.5 x 10(-3) M maltose, and 0.0125-0.1 mg   mL(-1) acorbose, respectively.	Maltose	267-274	hydroxyacid oxidase 1	Homo sapiens	118-121
21908639-9	2011	Consistent with this, ALY2- and UBP13-engineered cells of the industrial QA23 strain grew faster and produced more CO2 at 12 C than did the parental when maltose was used as the sole carbon source.	Maltose	154-161	Aly2p	Saccharomyces cerevisiae S288C	22-26
21908639-9	2011	Consistent with this, ALY2- and UBP13-engineered cells of the industrial QA23 strain grew faster and produced more CO2 at 12 C than did the parental when maltose was used as the sole carbon source.	Maltose	154-161	ubiquitin-specific protease UBP13	Saccharomyces cerevisiae S288C	32-37
21963484-8	2011	A single-cell isolate showed an 11% higher ethanol yield on sucrose in chemostat cultures than an isogenic SUC2 reference strain, while transcriptome analysis revealed elevated expression of AGT1, encoding a disaccharide-proton symporter, and other maltose-related genes.	Maltose	249-256	alpha-glucoside permease	Saccharomyces cerevisiae S288C	191-195
21989929-2	2011	This was achieved by insertion of circularly permuted fluorescent proteins into a bacterial periplasmic binding protein (PBP), Escherichia coli maltodextrin-binding protein, resulting in a four-color family of maltose indicators.	Maltose	210-217	EitA	Escherichia coli	92-119
21989929-2	2011	This was achieved by insertion of circularly permuted fluorescent proteins into a bacterial periplasmic binding protein (PBP), Escherichia coli maltodextrin-binding protein, resulting in a four-color family of maltose indicators.	Maltose	210-217	EitA	Escherichia coli	121-124
21087810-2	2011	Following the export into the cytosol, maltose acts as donor for a glucosyl transfer to cytosolic heteroglycans as mediated by a cytosolic transglucosidase (DPE2; EC 2.4.1.25) and the second glucosyl residue is liberated as glucose.	Maltose	39-46	DNA polymerase epsilon 2, accessory subunit	Homo sapiens	157-161
21659518-2	2011	Maltose-binding protein (MBP) is a large (a two-domain, 370-amino acid residue) bacterial periplasmic protein involved in maltose uptake.	Maltose	122-129	myelin basic protein	Homo sapiens	0-23
21659518-2	2011	Maltose-binding protein (MBP) is a large (a two-domain, 370-amino acid residue) bacterial periplasmic protein involved in maltose uptake.	Maltose	122-129	myelin basic protein	Homo sapiens	25-28
21659518-8	2011	In the case of maltose-bound MBP, the protein unfolds via the intermediate in 79% of the cases, the remaining 21% via path II.	Maltose	15-22	myelin basic protein	Homo sapiens	29-32
21755532-10	2011	Under the control of the AGT1 promoter of the ale strain the emergence of GFP was strongly induced by maltose, whereas only a low level of GFP was detected with the construct carrying the AGT1 promoter of the lager strain.	Maltose	102-109	alpha-glucoside permease	Saccharomyces cerevisiae S288C	25-29
21755532-11	2011	Thus, the extra MAL-activator binding element, present in the AGT1 promoter of the ale strain, appears to be necessary to reach a high level of induction by maltose.	Maltose	157-164	alpha-glucoside permease	Saccharomyces cerevisiae S288C	62-66
21242321-7	2011	Upon cold treatment, the Disproportionating Enzyme 2 (DPE2), a cytosolic transglucosidase metabolizing maltose to glucose, increased rapidly in the centrifugation pellet fraction and decreased in the soluble fraction.	Maltose	103-110	disproportionating enzyme 2	Arabidopsis thaliana	25-52
21745386-4	2011	RESULTS: An expression plasmid containing the open reading frame for tung tree (Vernicia fordii) DGAT1 fused to maltose binding protein and poly-histidine affinity tags was constructed and expressed in E. coli BL21(DE3).	Maltose	112-119	diacylglycerol O-acyltransferase 1	Rattus norvegicus	97-102
21714924-0	2011	Overexpression and purification of U24 from human herpesvirus type-6 in E. coli: unconventional use of oxidizing environments with a maltose binding protein-hexahistine dual tag to enhance membrane protein yield.	Maltose	133-140	small nucleolar RNA, C/D box 24	Homo sapiens	35-38
21420935-5	2011	To better understand structural and multifunctional roles of the PRR-IC, we report the crystal structure of the PRR-IC domain as maltose-binding protein (MBP) fusion proteins at 2.0A (maltose-free) and 2.15A (maltose-bound).	Maltose	129-136	ATPase H+ transporting accessory protein 2	Homo sapiens	65-68
21420935-5	2011	To better understand structural and multifunctional roles of the PRR-IC, we report the crystal structure of the PRR-IC domain as maltose-binding protein (MBP) fusion proteins at 2.0A (maltose-free) and 2.15A (maltose-bound).	Maltose	129-136	ATPase H+ transporting accessory protein 2	Homo sapiens	112-115
21420935-5	2011	To better understand structural and multifunctional roles of the PRR-IC, we report the crystal structure of the PRR-IC domain as maltose-binding protein (MBP) fusion proteins at 2.0A (maltose-free) and 2.15A (maltose-bound).	Maltose	129-136	myelin basic protein	Homo sapiens	154-157
21420935-5	2011	To better understand structural and multifunctional roles of the PRR-IC, we report the crystal structure of the PRR-IC domain as maltose-binding protein (MBP) fusion proteins at 2.0A (maltose-free) and 2.15A (maltose-bound).	Maltose	184-191	ATPase H+ transporting accessory protein 2	Homo sapiens	65-68
21420935-5	2011	To better understand structural and multifunctional roles of the PRR-IC, we report the crystal structure of the PRR-IC domain as maltose-binding protein (MBP) fusion proteins at 2.0A (maltose-free) and 2.15A (maltose-bound).	Maltose	184-191	ATPase H+ transporting accessory protein 2	Homo sapiens	112-115
21420935-5	2011	To better understand structural and multifunctional roles of the PRR-IC, we report the crystal structure of the PRR-IC domain as maltose-binding protein (MBP) fusion proteins at 2.0A (maltose-free) and 2.15A (maltose-bound).	Maltose	184-191	myelin basic protein	Homo sapiens	154-157
21496351-4	2011	RESULTS: We performed phage display analysis with the purified recombinant AC3 protein with Maltose Binding Protein as fusion tag (MBP-AC3).	Maltose	92-99	AC3	Tomato leaf curl Kerala virus	75-78
21378967-2	2011	sABs that preferentially recognize the maltose-bound form of MBP act as positive allosteric effectors by substantially increasing the affinity for maltose.	Maltose	39-46	myelin basic protein	Homo sapiens	61-64
21378967-2	2011	sABs that preferentially recognize the maltose-bound form of MBP act as positive allosteric effectors by substantially increasing the affinity for maltose.	Maltose	147-154	myelin basic protein	Homo sapiens	61-64
21378967-4	2011	We show that sABs that recognize the bound form of MBP can rescue the function of a binding-deficient mutant by restoring its natural affinity for maltose.	Maltose	147-154	myelin basic protein	Homo sapiens	51-54
21487098-10	2011	Furthermore, we speculate that BZR1-BAMs may transmit metabolic signals by binding a ligand in their BAM domain, although diurnal changes in the concentration of maltose, a candidate ligand produced by chloroplastic beta-amylases, do not influence their transcription factor function.	Maltose	162-169	Brassinosteroid signaling positive regulator (BZR1) family protein	Arabidopsis thaliana	31-35
21242321-7	2011	Upon cold treatment, the Disproportionating Enzyme 2 (DPE2), a cytosolic transglucosidase metabolizing maltose to glucose, increased rapidly in the centrifugation pellet fraction and decreased in the soluble fraction.	Maltose	103-110	disproportionating enzyme 2	Arabidopsis thaliana	54-58
21242321-9	2011	These results support a model that cold-induced inactivation of DPE2 leads to rapid accumulation of maltose, which is a cold-induced compatible solute that protects cells from freezing damage.	Maltose	100-107	disproportionating enzyme 2	Arabidopsis thaliana	64-68
22096548-5	2011	We have previously demonstrated that the non-homologous recombination of the genes encoding maltose binding protein (MBP) and TEM1 beta-lactamase (BLA) can result in fusion proteins in which beta-lactamase enzyme activity is allosterically regulated by maltose.	Maltose	92-99	myelin basic protein	Homo sapiens	117-120
21206039-1	2011	Maltoporin is an outer-membrane protein that forms a beta-barrel composed of three monomers and ensures the transport of maltose and maltodextrin in Gram-negative bacteria.	Maltose	121-128	maltoporin	Escherichia coli	0-10
21098673-12	2011	Our results suggest that the alpha-glucosidase HvAGL97 is the major endosperm enzyme catalyzing the conversion of maltose to Glc but is not required for starch degradation.	Maltose	114-121	Agl1	Hordeum vulgare	29-46
20971850-4	2010	Here, we demonstrate that the maltose binding protein (MalE) lacking its natural export signal and fused to the HlyA secretion signal is poorly secreted by the Hly system.	Maltose	30-37	hemolysin A	Escherichia coli	112-116
20581222-6	2010	The alpha-glucosidase, a member of GH31 family, shows substrate preference for alpha(1-6) over alpha(1-4) glycosidic linkages and produces glucose from isomaltose as well as maltose.	Maltose	155-162	sucrase-isomaltase	Homo sapiens	4-21
21058632-1	2010	High-level heterologous expression of human 1alpha,25-dihydroxyvitamin D(3) 24-hydroxylase (CYP24A1) in Escherichia coli was attained via a fusion construct by appending the mature CYP24A1 without the leader sequence to the maltose binding protein (MBP).	Maltose	224-231	cytochrome P450 family 24 subfamily A member 1	Homo sapiens	92-99
20967220-1	2010	BACKGROUND: The digestion of dietary starch in humans is initiated by salivary alpha-amylase, an endo-enzyme that hydrolyzes starch into maltose, maltotriose and larger oligosaccharides.	Maltose	137-144	amylase alpha 1A	Homo sapiens	70-92
20542276-1	2010	The goal of the present work is to apply the versatile asymmetrical flow field-flow fractionation (AF4) coupled to UV and light scattering detection for the characterization of hyperbranched poly(ethylene imine) decorated with maltose shell (PEI-Mal) and the polar dye Rose Bengal (RB) in respect to their complexation behaviour.	Maltose	227-234	AF4/FMR2 family member 1	Homo sapiens	99-102
20735059-5	2010	On the basis of this property, a bienzyme biosensing system for the detection of maltose was fabricated by successive LbL assembly of graphene, glucose oxidase (GOx), and glucoamylase (GA).	Maltose	81-88	hydroxyacid oxidase 1	Homo sapiens	144-159
20735059-5	2010	On the basis of this property, a bienzyme biosensing system for the detection of maltose was fabricated by successive LbL assembly of graphene, glucose oxidase (GOx), and glucoamylase (GA).	Maltose	81-88	hydroxyacid oxidase 1	Homo sapiens	161-164
20600753-13	2010	RESULTS: NSF extract showed potent rat intestinal alpha-glucosidase inhibitory activity for maltose hydrolysis with ED(50) value of 0.1 mg/ml.	Maltose	92-99	N-ethylmaleimide sensitive factor, vesicle fusing ATPase	Rattus norvegicus	9-12
20600753-14	2010	In Caco-2 monolayer, alpha-glucosidase activity for the maltose hydrolysis was down-regulated by NSF extract at a concentration of 0.05 mg/well level, showing 74% inhibition compared to the saline treated control.	Maltose	56-63	N-ethylmaleimide sensitive factor, vesicle fusing ATPase	Rattus norvegicus	97-100
20695638-3	2010	In control samples, maltose and maltotriose were hydrolyzed by alpha-glucosidase and not beta-galactosidase, whereas lactose was resistant to alpha-glucosidase but was hydrolyzed with beta-galactosidase.	Maltose	20-27	sucrase-isomaltase	Homo sapiens	63-80
20080449-0	2010	Maltose biosensing based on co-immobilization of alpha-glucosidase and pyranose oxidase.	Maltose	0-7	sucrase-isomaltase	Homo sapiens	49-66
20080449-1	2010	A new bi-enzymatic system was designed by co-immobilization of alpha-glucosidase (AG) and pyranose oxidase (PyOx) for maltose analysis.	Maltose	118-125	sucrase-isomaltase	Homo sapiens	63-80
20080449-1	2010	A new bi-enzymatic system was designed by co-immobilization of alpha-glucosidase (AG) and pyranose oxidase (PyOx) for maltose analysis.	Maltose	118-125	sucrase-isomaltase	Homo sapiens	82-84
20466650-4	2010	To understand the molecular requirements for the observed promiscuity of the malectin domain, here we analyze the binding to a range of diglucosides through comparison of the protein chemical shift perturbation patterns and the saturation transfer difference spectra of the ligands including two maltose-mimicking drugs.	Maltose	296-303	malectin	Homo sapiens	77-85
20466650-5	2010	A comparison of the maltose-bound structure of the malectin domain with the complex of the native ligand nigerose reveals why malectin is able to tolerate such a diversity of ligands.	Maltose	20-27	malectin	Homo sapiens	51-59
20466650-5	2010	A comparison of the maltose-bound structure of the malectin domain with the complex of the native ligand nigerose reveals why malectin is able to tolerate such a diversity of ligands.	Maltose	20-27	malectin	Homo sapiens	126-134
20562106-11	2010	Expressions of IMA1 and IMA5/YJL216c were strongly induced by maltose, isomaltose, and alpha-methylglucopyranoside, in accordance with their regulation by the Malx3p-transcription system.	Maltose	62-69	oligo-1,6-glucosidase IMA1	Saccharomyces cerevisiae S288C	15-19
20562106-11	2010	Expressions of IMA1 and IMA5/YJL216c were strongly induced by maltose, isomaltose, and alpha-methylglucopyranoside, in accordance with their regulation by the Malx3p-transcription system.	Maltose	62-69	oligo-1,6-glucosidase IMA5	Saccharomyces cerevisiae S288C	24-28
19880212-11	2010	SP-D-binding to viable and early apoptotic neutrophils was inhibited by maltose and ethylene-diamin-tetra-acetate (EDTA), suggesting lectin-binding site involvement whereas the binding to late apoptotic neutrophils was predominantly Ca(2+)-independent.	Maltose	72-79	surfactant protein D	Homo sapiens	0-4
20564191-7	2010	The apparent affinity of extracellular glucose to Snf3 was measured for cells grown in non-fermentative medium or on maltose.	Maltose	117-124	glucose sensor	Saccharomyces cerevisiae S288C	50-54
20034108-1	2010	RG13 is a 72 kDa engineered allosteric enzyme comprised of a fusion between maltose binding protein (MBP) and TEM1 beta-lactamase (BLA) for which maltose is a positive effector of BLA activity.	Maltose	76-83	myelin basic protein	Homo sapiens	101-104
20180115-3	2010	The introduction of AGT1 allows maltose and maltotriose fermentation as well as the improvement of amylase activities.	Maltose	32-39	alpha-glucoside permease	Saccharomyces cerevisiae S288C	20-24
20402791-8	2010	When functional AGT1 from an ale strain was expressed in a lager strain, the resultant maltose transport activity had the high temperature dependence characteristic of ale yeasts.	Maltose	87-94	alpha-glucoside permease	Saccharomyces cerevisiae S288C	16-20
20402791-9	2010	Lager yeast MTT1 and MALx1 genes were expressed in a maltose-negative laboratory strain of S. cerevisiae.	Maltose	53-60	RNA helicase	Saccharomyces cerevisiae S288C	12-16
20147285-2	2010	To determine whether direct interactions between the translocated sugar and MalFGK(2) are important for the regulation of ATP hydrolysis, we used an MBP mutant (sMBP) that is able to bind either maltose or sucrose.	Maltose	195-202	myelin basic protein	Homo sapiens	149-152
20147285-2	2010	To determine whether direct interactions between the translocated sugar and MalFGK(2) are important for the regulation of ATP hydrolysis, we used an MBP mutant (sMBP) that is able to bind either maltose or sucrose.	Maltose	195-202	transmembrane 9 superfamily member 3	Homo sapiens	161-165
20147285-3	2010	We observed that maltose- and sucrose-bound sMBP stimulate equal levels of MalFGK(2) ATPase activity.	Maltose	17-24	transmembrane 9 superfamily member 3	Homo sapiens	44-48
20147285-4	2010	Therefore, the ATPase activity of MalFGK(2) is coupled to translocation of maltose solely by interactions between MalFGK(2) and MBP.	Maltose	75-82	myelin basic protein	Homo sapiens	128-131
20147285-5	2010	For both maltose and sucrose, the ability of sMBP to stimulate the MalFGK(2) ATPase was greatly reduced compared with wild-type MBP, indicating that the mutations in sMBP have interfered with important interactions between MBP and MalFGK(2).	Maltose	9-16	transmembrane 9 superfamily member 3	Homo sapiens	45-49
20147285-5	2010	For both maltose and sucrose, the ability of sMBP to stimulate the MalFGK(2) ATPase was greatly reduced compared with wild-type MBP, indicating that the mutations in sMBP have interfered with important interactions between MBP and MalFGK(2).	Maltose	9-16	myelin basic protein	Homo sapiens	46-49
20147285-5	2010	For both maltose and sucrose, the ability of sMBP to stimulate the MalFGK(2) ATPase was greatly reduced compared with wild-type MBP, indicating that the mutations in sMBP have interfered with important interactions between MBP and MalFGK(2).	Maltose	9-16	transmembrane 9 superfamily member 3	Homo sapiens	166-170
20189250-3	2010	We constructed, expressed, and purified a recombinant immunogen, CD20ECD-6, which displays six tandemly repeated copies of the C-terminus of the murine CD20 ECD covalently linked to maltose-binding protein.	Maltose	182-189	membrane-spanning 4-domains, subfamily A, member 1	Mus musculus	65-69
19946617-4	2009	The maltose excess 1 mutant (mex1), which lacks the chloroplast envelope maltose transporter, accumulates high levels of maltose and starch in chloroplasts and develops a distinctive but previously unexplained chlorotic phenotype as leaves mature.	Maltose	4-11	root cap 1 (RCP1)	Arabidopsis thaliana	29-33
20171176-3	2010	We report that GTPase active AtDRP1A purified from Escherichia coli as a fusion to maltose binding protein forms homopolymers visible by negative staining electron microscopy.	Maltose	83-90	dynamin-like protein	Arabidopsis thaliana	29-36
19733183-6	2009	MBP consists of two lobes connected by a hinge region that move from an open to a closed conformation when the ligand maltose binds.	Maltose	118-125	myelin basic protein	Homo sapiens	0-3
20012864-3	2010	The expression of the FLO and MAL genes, which are important for the performance of yeast during industrial fermentations, is affected by complex proteins associated with Set1 (COMPASS) resulting in the induction of flocculation and improved maltose fermentation capacity during the early stages of high-gravity fermentation.	Maltose	242-249	histone methyltransferase SET1	Saccharomyces cerevisiae S288C	171-175
20059115-1	2009	The low-frequency (omega<400 cm(-1)) vibrational properties of lysozyme in aqueous solutions of three well-known protecting sugars, namely, trehalose, maltose, and sucrose, have been investigated by means of complementary Raman scattering experiments and molecular dynamics simulations.	Maltose	154-161	lysozyme	Homo sapiens	66-74
19928952-1	2009	A robust method to immobilize a maltose biosensor is described using an engineered maltose periplasmic binding protein (PBP) covalently coupled to NBDamide, an environmentally sensitive fluorophore.	Maltose	32-39	phosphatidylethanolamine binding protein 1	Homo sapiens	91-118
19928952-1	2009	A robust method to immobilize a maltose biosensor is described using an engineered maltose periplasmic binding protein (PBP) covalently coupled to NBDamide, an environmentally sensitive fluorophore.	Maltose	32-39	phosphatidylethanolamine binding protein 1	Homo sapiens	120-123
19946617-4	2009	The maltose excess 1 mutant (mex1), which lacks the chloroplast envelope maltose transporter, accumulates high levels of maltose and starch in chloroplasts and develops a distinctive but previously unexplained chlorotic phenotype as leaves mature.	Maltose	73-80	root cap 1 (RCP1)	Arabidopsis thaliana	29-33
19946617-5	2009	The introduction of additional mutations that prevent starch synthesis, or that block maltose production from starch, also prevent chlorosis of mex1.	Maltose	86-93	root cap 1 (RCP1)	Arabidopsis thaliana	144-148
19682975-3	2009	To the best of our knowledge, this is the first report to provide information regarding the biological distance between the two lobes of MBP upon maltose binding.	Maltose	146-153	myelin basic protein	Homo sapiens	137-140
19946617-6	2009	In contrast, introduction of mutations in disproportionating enzyme (DPE1) results in the accumulation of maltotriose in addition to maltose, and greatly increases chlorosis.	Maltose	133-140	disproportionating enzyme	Arabidopsis thaliana	69-73
19682975-5	2009	After the FRET reaction, maltose-treated MBP was shown to exhibit a considerable energy transfer (FRET efficiency (E)= approximately 0.11, Distance (D)= approximately 6.93 nm) at the ensemble level, which was regarded as reflective of the increase in donor quenching and the upshift in acceptor emission intensity, thereby suggesting that the donor and the acceptor had been brought close together as the result of structural alterations in MBP.	Maltose	25-32	myelin basic protein	Homo sapiens	41-44
19682975-5	2009	After the FRET reaction, maltose-treated MBP was shown to exhibit a considerable energy transfer (FRET efficiency (E)= approximately 0.11, Distance (D)= approximately 6.93 nm) at the ensemble level, which was regarded as reflective of the increase in donor quenching and the upshift in acceptor emission intensity, thereby suggesting that the donor and the acceptor had been brought close together as the result of structural alterations in MBP.	Maltose	25-32	myelin basic protein	Homo sapiens	441-444
19682975-6	2009	However, upon glucose treatment, no FRET phenomenon was detected, thereby implying the specificity of interaction between MBP and maltose.	Maltose	130-137	myelin basic protein	Homo sapiens	122-125
19682975-8	2009	Therefore, our data showed that maltose-stimulated conformational changes of MBP could be measured by FRET, thereby providing biological information, including the FRET efficiency and the intramolecular distance.	Maltose	32-39	myelin basic protein	Homo sapiens	77-80
19630440-2	2009	Binding of maltose to MBP brings about a conformational change from open to closed that leads to a strong stimulation of the MalFGK(2) ATPase.	Maltose	11-18	myelin basic protein	Homo sapiens	22-25
19630440-6	2009	The effect of MBP concentration on the stimulation of MalFGK(2) was assessed: for unliganded MBP, the apparent K(M) for stimulation of MalFGK(2) was below 1 microM, while for maltose-bound MBP, the K(M) was approximately 15 microM.	Maltose	175-182	myelin basic protein	Homo sapiens	14-17
19657968-6	2009	Galectin-2 was released more effectively from the membrane by lactose than was galectin-4, and surprisingly, it was also released by the noncanonical disaccharides sucrose and maltose.	Maltose	176-183	galectin 2	Sus scrofa	0-10
19052253-5	2009	Transient gene expression assays reveal that the promoter activity of the TXNIP gene is upregulated by glucose, 3-O-methylglucose, and maltose, but not by mannitol.	Maltose	135-142	thioredoxin interacting protein	Homo sapiens	74-79
19420711-2	2009	The simultaneous oral administration of the extract at a dose of 1.0 mg/mouse with maltose or sucrose inhibited the postprandial elevation of the plasma glucose and insulin levels and intestinal alpha-glucosidase activities in mice.	Maltose	83-90	sucrase isomaltase (alpha-glucosidase)	Mus musculus	195-212
19249874-2	2009	Although SP-D shows a preference for glucose/maltose, the protein also recognizes d-mannose and a variety of mannose-rich microbial ligands.	Maltose	45-52	surfactant protein D	Homo sapiens	9-13
19301314-5	2009	Fluorescence measurements revealed that MBP containing a BODIPY-FL moiety in place of Tyr210 showed a 13-fold increase in fluorescence upon binding of maltose.	Maltose	151-158	myelin basic protein	Homo sapiens	40-43
19301314-7	2009	MBP containing a BODIPY-558 moiety also showed a maltose-dependent increase in fluorescence.	Maltose	49-56	myelin basic protein	Homo sapiens	0-3
18983838-5	2009	The ABCB1 purification procedure was optimised to allow successful freeze drying by substitution of glycerol with the disaccharides trehalose or maltose.	Maltose	145-152	ATP binding cassette subfamily B member 1	Homo sapiens	4-9
18983838-7	2009	However, during storage trehalose preserved ATPase activity for several months regardless of the temperature (e.g. 60% retention at 150 days), whereas ATPase activity in maltose purified P-gp was affected by both storage time and temperature.	Maltose	170-177	dynein axonemal heavy chain 8	Homo sapiens	151-157
18983838-7	2009	However, during storage trehalose preserved ATPase activity for several months regardless of the temperature (e.g. 60% retention at 150 days), whereas ATPase activity in maltose purified P-gp was affected by both storage time and temperature.	Maltose	170-177	ATP binding cassette subfamily B member 1	Homo sapiens	187-191
19384925-2	2009	In this study, a series of sugars, including sucrose, lactose, trehalose, maltose, fructose, galactose, fucose, mannose, and glucose were studied by modulated DSC and freeze-dry microscopy in order to better understand whether sucrose is unique in any way with respect to this behavior, as well as to explore the physical basis, and the pharmaceutical significance of these multiple transitions.	Maltose	74-81	desmocollin 3	Homo sapiens	159-162
19475663-4	2009	By chaperoning IAPP through fusion to maltose binding protein, we find that IAPP can adopt a alpha-helical structure at residues 8-18 and 22-27 and that molecules of IAPP dimerize.	Maltose	38-45	islet amyloid polypeptide	Homo sapiens	15-19
19475663-4	2009	By chaperoning IAPP through fusion to maltose binding protein, we find that IAPP can adopt a alpha-helical structure at residues 8-18 and 22-27 and that molecules of IAPP dimerize.	Maltose	38-45	islet amyloid polypeptide	Homo sapiens	76-80
19475663-4	2009	By chaperoning IAPP through fusion to maltose binding protein, we find that IAPP can adopt a alpha-helical structure at residues 8-18 and 22-27 and that molecules of IAPP dimerize.	Maltose	38-45	islet amyloid polypeptide	Homo sapiens	76-80
19181838-0	2009	Improved fermentation performance of a lager yeast after repair of its AGT1 maltose and maltotriose transporter genes.	Maltose	76-83	alpha-glucoside permease	Saccharomyces cerevisiae S288C	71-75
19181838-3	2009	alpha-Glucosides are transported into Saccharomyces yeasts by several transporters, including Agt1, which is a good carrier of both maltose and maltotriose.	Maltose	132-139	alpha-glucoside permease	Saccharomyces cerevisiae S288C	94-98
19181838-6	2009	Compared to the untransformed strain, the transformants with repaired AGT1 had higher maltose transport activity, especially after growth on glucose (which represses endogenous alpha-glucoside transporter genes) and higher ratios of maltotriose transport activity to maltose transport activity.	Maltose	86-93	alpha-glucoside permease	Saccharomyces cerevisiae S288C	70-74
19181838-6	2009	Compared to the untransformed strain, the transformants with repaired AGT1 had higher maltose transport activity, especially after growth on glucose (which represses endogenous alpha-glucoside transporter genes) and higher ratios of maltotriose transport activity to maltose transport activity.	Maltose	267-274	alpha-glucoside permease	Saccharomyces cerevisiae S288C	70-74
19127343-4	2009	In a second rhamnose-inducible vector, the S. cerevisiae Ulp1 protease gene for processing Smt3 fusion proteins was fused in the same way to maltose-binding protein and His-tag sequence but without the Smt3 gene.	Maltose	141-148	SUMO protease ULP1	Saccharomyces cerevisiae S288C	57-61
19127343-4	2009	In a second rhamnose-inducible vector, the S. cerevisiae Ulp1 protease gene for processing Smt3 fusion proteins was fused in the same way to maltose-binding protein and His-tag sequence but without the Smt3 gene.	Maltose	141-148	SUMO family protein SMT3	Saccharomyces cerevisiae S288C	91-95
19059402-0	2009	An ISFET biosensor for the monitoring of maltose-induced conformational changes in MBP.	Maltose	41-48	myelin basic protein	Homo sapiens	83-86
19059402-1	2009	Here we describe an ion sensitive field effect transistor (ISFET) biosensor, which was designed to monitor directly the surface charge of structurally altered maltose binding protein (MBP) upon stimulation with maltose.	Maltose	159-166	myelin basic protein	Homo sapiens	184-187
19059402-4	2009	Collectively, our results clearly suggest that ISFET provide a high fidelity system for the detection of maltose-induced structural alterations in MBP.	Maltose	105-112	myelin basic protein	Homo sapiens	147-150
19565324-2	2009	First, a maltose-binding protein fused to DV2 C protein (MBP-C) was overproduced in E. coli.	Maltose	9-16	mannose-binding lectin (protein C) 2	Mus musculus	57-62
18776201-7	2008	Plants of the Arabidopsis maltose excess1-1 mutant, which is homozygous for a defective MEX1 allele, were transformed with the 35S:MdMEX:GFP construct.	Maltose	26-33	root cap 1 (RCP1)	Arabidopsis thaliana	88-92
19026541-3	2008	Disruption of Gr5a prevents the detection of trehalose [1-3], whereas mutation of Gr64a impairs the responses to sucrose, maltose, and glucose [4, 5].	Maltose	122-129	Gustatory receptor 64a	Drosophila melanogaster	82-87
19026541-6	2008	Gr64f was also required in concert with Gr64a to rescue the defects in the sensitivities to sucrose, maltose, and glucose, resulting from deletion of the entire Gr64 cluster.	Maltose	101-108	Gustatory receptor 64f	Drosophila melanogaster	0-5
19026541-6	2008	Gr64f was also required in concert with Gr64a to rescue the defects in the sensitivities to sucrose, maltose, and glucose, resulting from deletion of the entire Gr64 cluster.	Maltose	101-108	Gustatory receptor 64a	Drosophila melanogaster	40-45
19389514-2	2009	Presently, one of SLA-I gene SLA-2 and beta(2)m gene were expressed as soluble maltose binding proteins (MBP-proteins) in a pMAL-p2X/Escherichia coli TB1 system and identified by western blotting with anti-MBP polyclonal antibodies.	Maltose	79-86	Src like adaptor 2	Homo sapiens	29-34
19389514-2	2009	Presently, one of SLA-I gene SLA-2 and beta(2)m gene were expressed as soluble maltose binding proteins (MBP-proteins) in a pMAL-p2X/Escherichia coli TB1 system and identified by western blotting with anti-MBP polyclonal antibodies.	Maltose	79-86	beta-2-microglobulin	Homo sapiens	39-47
19389514-2	2009	Presently, one of SLA-I gene SLA-2 and beta(2)m gene were expressed as soluble maltose binding proteins (MBP-proteins) in a pMAL-p2X/Escherichia coli TB1 system and identified by western blotting with anti-MBP polyclonal antibodies.	Maltose	79-86	myelin basic protein	Homo sapiens	105-108
19160454-2	2008	In one particular fast maltose-fermenting yeast strain, with constitutive expression of FLO11, the expression of FLO1, FLO5 and FLO9 was induced during fermentation of high concentrations of maltose or glucose.	Maltose	23-30	Flo11p	Saccharomyces cerevisiae S288C	88-93
19160454-2	2008	In one particular fast maltose-fermenting yeast strain, with constitutive expression of FLO11, the expression of FLO1, FLO5 and FLO9 was induced during fermentation of high concentrations of maltose or glucose.	Maltose	23-30	flocculin FLO1	Saccharomyces cerevisiae S288C	88-92
19160454-2	2008	In one particular fast maltose-fermenting yeast strain, with constitutive expression of FLO11, the expression of FLO1, FLO5 and FLO9 was induced during fermentation of high concentrations of maltose or glucose.	Maltose	23-30	flocculin FLO5	Saccharomyces cerevisiae S288C	119-123
19160454-2	2008	In one particular fast maltose-fermenting yeast strain, with constitutive expression of FLO11, the expression of FLO1, FLO5 and FLO9 was induced during fermentation of high concentrations of maltose or glucose.	Maltose	191-198	Flo11p	Saccharomyces cerevisiae S288C	88-93
19160454-2	2008	In one particular fast maltose-fermenting yeast strain, with constitutive expression of FLO11, the expression of FLO1, FLO5 and FLO9 was induced during fermentation of high concentrations of maltose or glucose.	Maltose	191-198	flocculin FLO1	Saccharomyces cerevisiae S288C	88-92
19160454-2	2008	In one particular fast maltose-fermenting yeast strain, with constitutive expression of FLO11, the expression of FLO1, FLO5 and FLO9 was induced during fermentation of high concentrations of maltose or glucose.	Maltose	191-198	flocculin FLO5	Saccharomyces cerevisiae S288C	119-123
18715992-6	2008	Here we present the first crystal structure of a RACK1 protein, RACK1 isoform A from Arabidopsis thaliana, at 2.4 A resolution, as a C-terminal fusion of the maltose binding protein.	Maltose	158-165	receptor for activated C kinase 1	Homo sapiens	49-54
18715992-6	2008	Here we present the first crystal structure of a RACK1 protein, RACK1 isoform A from Arabidopsis thaliana, at 2.4 A resolution, as a C-terminal fusion of the maltose binding protein.	Maltose	158-165	receptor for activated C kinase 1	Homo sapiens	64-69
17950243-2	2008	The interaction between MBP and MalFGK(2) has a critical role in maltose transport, but a coherent description of the interaction is complicated because both MBP and MalFGK(2) can adopt multiple conformations.	Maltose	65-72	myelin basic protein	Homo sapiens	24-27
17950243-2	2008	The interaction between MBP and MalFGK(2) has a critical role in maltose transport, but a coherent description of the interaction is complicated because both MBP and MalFGK(2) can adopt multiple conformations.	Maltose	65-72	myelin basic protein	Homo sapiens	158-161
17950243-4	2008	The most important feature of this model is that ligand-bound MBP initiates the process of ATP-dependent maltose transport by stabilizing a high-energy conformation of MalFGK(2).	Maltose	105-112	myelin basic protein	Homo sapiens	62-65
17950243-7	2008	In ABC export systems, which do not use a binding protein, the substrate itself is expected to play a role similar to ligand-bound MBP in the maltose transport system.	Maltose	142-149	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	3-6
17950243-7	2008	In ABC export systems, which do not use a binding protein, the substrate itself is expected to play a role similar to ligand-bound MBP in the maltose transport system.	Maltose	142-149	myelin basic protein	Homo sapiens	131-134
21261860-3	2008	Overall, we found that: (i) export efficiency and periplasmic yield of a model substrate were affected by the composition of the Tat signal peptide, (ii) Tat substrates were correctly processed at their N-termini upon reaching the periplasm and (iii) proteins fused to maltose-binding protein (MBP) were reliably exported by the Tat system, but only when correctly folded; aberrantly folded MBP fusions were excluded by the Tat pathway"s folding quality control feature.	Maltose	269-276	twin-arginine translocation (TAT) pathway signal sequence domain protein	Escherichia coli	154-157
18618272-6	2008	LjSUT4 transported a range of glucosides including sucrose, salicin, helicin, maltose, sucralose and both alpha- and beta-linked synthetic phenyl glucosides.	Maltose	78-85	sut4	Lotus japonicus	0-6
18499663-6	2008	Here we show that DPE2 transfers the non-reducing glucosyl unit from maltose to glycogen by a ping-pong mechanism.	Maltose	69-76	DNA polymerase epsilon 2, accessory subunit	Homo sapiens	18-22
21261860-3	2008	Overall, we found that: (i) export efficiency and periplasmic yield of a model substrate were affected by the composition of the Tat signal peptide, (ii) Tat substrates were correctly processed at their N-termini upon reaching the periplasm and (iii) proteins fused to maltose-binding protein (MBP) were reliably exported by the Tat system, but only when correctly folded; aberrantly folded MBP fusions were excluded by the Tat pathway"s folding quality control feature.	Maltose	269-276	twin-arginine translocation (TAT) pathway signal sequence domain protein	Escherichia coli	154-157
21261860-3	2008	Overall, we found that: (i) export efficiency and periplasmic yield of a model substrate were affected by the composition of the Tat signal peptide, (ii) Tat substrates were correctly processed at their N-termini upon reaching the periplasm and (iii) proteins fused to maltose-binding protein (MBP) were reliably exported by the Tat system, but only when correctly folded; aberrantly folded MBP fusions were excluded by the Tat pathway"s folding quality control feature.	Maltose	269-276	twin-arginine translocation (TAT) pathway signal sequence domain protein	Escherichia coli	154-157
18359840-6	2008	suc1 mutants accumulated less anthocyanins in response to exogenous sucrose or maltose and microarray analysis revealed reduced expression of many genes important for anthocyanin biosynthesis.	Maltose	79-86	sucrose-proton symporter 1	Arabidopsis thaliana	0-4
18374320-6	2008	In an in vivo study using Goto-Kakizaki (GK) rats, the acetone extract was found to be a potent inhibitor of alpha-glucosidase hydrolysis of maltose when compared to untreated control animals.	Maltose	141-148	sucrase-isomaltase	Homo sapiens	109-126
18458105-3	2008	This report demonstrates, in vivo, the association of the Saccharomyces cerevisiae maltose-responsive transcription activator Mal63 (MAL-activator) with the yeast Hsp70 (Ssa1), Hsp90 (Hsp82), and Hop (Sti1) homologs, using a collection of inducible, constitutive, and noninducible alleles.	Maltose	83-90	Hsp70 family ATPase SSA1	Saccharomyces cerevisiae S288C	170-174
18458105-3	2008	This report demonstrates, in vivo, the association of the Saccharomyces cerevisiae maltose-responsive transcription activator Mal63 (MAL-activator) with the yeast Hsp70 (Ssa1), Hsp90 (Hsp82), and Hop (Sti1) homologs, using a collection of inducible, constitutive, and noninducible alleles.	Maltose	83-90	Hsp90 family chaperone HSP82	Saccharomyces cerevisiae S288C	177-182
18458105-3	2008	This report demonstrates, in vivo, the association of the Saccharomyces cerevisiae maltose-responsive transcription activator Mal63 (MAL-activator) with the yeast Hsp70 (Ssa1), Hsp90 (Hsp82), and Hop (Sti1) homologs, using a collection of inducible, constitutive, and noninducible alleles.	Maltose	83-90	Hsp90 family chaperone HSP82	Saccharomyces cerevisiae S288C	184-189
18458105-3	2008	This report demonstrates, in vivo, the association of the Saccharomyces cerevisiae maltose-responsive transcription activator Mal63 (MAL-activator) with the yeast Hsp70 (Ssa1), Hsp90 (Hsp82), and Hop (Sti1) homologs, using a collection of inducible, constitutive, and noninducible alleles.	Maltose	83-90	Hsp90 cochaperone STI1	Saccharomyces cerevisiae S288C	201-205
18329038-2	2008	The cyanine dyes Cy5 and Cy5.5 were used as a donor-acceptor pair by conjugation to maltose-labeled bovine serum albumin (BSA) and the monoclonal antibody IgG 39.5, giving Cy5-BSA-maltotriitol (3.1/1/18) and Cy5.5-mAb39.5 (2.2/1), respectively.	Maltose	84-91	albumin	Homo sapiens	107-120
18313049-6	2008	The cell-free system with pure components reveals that recombinant RNF43 fused with maltose-binding protein has autoubiquitylation activity.	Maltose	84-91	ring finger protein 43	Homo sapiens	67-72
18061677-3	2008	The CRD of human Langerin, which was expressed as a soluble protein in the periplasm of E. coli, was crystallized both alone and in the presence of two sugars, followed by X-ray analyses to resolutions of 2.5A for apo-Langerin and to 1.6A and 2.1A for the complexes with mannose and maltose, respectively.	Maltose	283-290	CD207 molecule	Homo sapiens	17-25
18390594-8	2008	The bam3 mutant had elevated starch levels and lower nighttime maltose levels than the wild type, whereas bam1 did not.	Maltose	63-70	Leucine-rich receptor-like protein kinase family protein	Arabidopsis thaliana	4-8
18226920-1	2008	A specialized vector backbone from the Protein Structure Initiative was used to express full-length human cytochrome b5 as a C-terminal fusion to His8-maltose binding protein in Escherichia coli.	Maltose	151-158	cytochrome b5 type A	Homo sapiens	106-119
18284212-11	2008	In particular, nitrite-substituted human pancreatic alpha-amylase demonstrates the unique ability to cleave acarbose into its acarviosine and maltose parts and carry out a previously unseen product elongation.	Maltose	142-149	amylase alpha 2A	Homo sapiens	41-65
18193902-5	2008	Changes in amino acid-assigned peaks before and after MBP-Ag4 bound maltose were used to assess protein orientation on the surface of silver nanoparticles.	Maltose	68-75	myelin basic protein	Homo sapiens	54-57
18203856-5	2008	While both high- and low-affinity transport activities were responsible for maltose uptake from the medium, in the case of maltotriose, the only low-affinity (K(m), 36 +/- 2 mM) transport activity was mediated by the AGT1 permease.	Maltose	76-83	alpha-glucoside permease	Saccharomyces cerevisiae S288C	217-221
18252249-1	2008	The putative Drosophila (D.) melanogaster gene ortholog of mammalian succinic semialdehyde dehydrogenase (SSADH, EC1.2.1.24; NM_143151) that is involved in the degradation of the neurotransmitter GABA, and the putative D. melanogaster aldehyde dehydrogenase gene Aldh (NM_135441) were cloned and expressed as enzymatically active maltose binding protein (MalE) fusion products in Escherichia coli.	Maltose	330-337	aldehyde dehydrogenase 5 family member A1	Homo sapiens	69-104
18252249-1	2008	The putative Drosophila (D.) melanogaster gene ortholog of mammalian succinic semialdehyde dehydrogenase (SSADH, EC1.2.1.24; NM_143151) that is involved in the degradation of the neurotransmitter GABA, and the putative D. melanogaster aldehyde dehydrogenase gene Aldh (NM_135441) were cloned and expressed as enzymatically active maltose binding protein (MalE) fusion products in Escherichia coli.	Maltose	330-337	aldehyde dehydrogenase 5 family member A1	Homo sapiens	106-111
18252249-1	2008	The putative Drosophila (D.) melanogaster gene ortholog of mammalian succinic semialdehyde dehydrogenase (SSADH, EC1.2.1.24; NM_143151) that is involved in the degradation of the neurotransmitter GABA, and the putative D. melanogaster aldehyde dehydrogenase gene Aldh (NM_135441) were cloned and expressed as enzymatically active maltose binding protein (MalE) fusion products in Escherichia coli.	Maltose	330-337	Aldehyde dehydrogenase	Drosophila melanogaster	82-104
18252249-1	2008	The putative Drosophila (D.) melanogaster gene ortholog of mammalian succinic semialdehyde dehydrogenase (SSADH, EC1.2.1.24; NM_143151) that is involved in the degradation of the neurotransmitter GABA, and the putative D. melanogaster aldehyde dehydrogenase gene Aldh (NM_135441) were cloned and expressed as enzymatically active maltose binding protein (MalE) fusion products in Escherichia coli.	Maltose	330-337	Aldehyde dehydrogenase	Drosophila melanogaster	263-267
18166050-8	2008	In uracil and 4-cyano-4"-ethynylbiphenyl, the CH hydrogen-bonding donors are sp2 and sp hybridized, respectively; a comparison of the calculated changes in 1H chemical shift with those for the sp3 hybridized CH donors in maltose (Yates et al.	Maltose	221-228	Sp2 transcription factor	Homo sapiens	77-80
18166050-8	2008	In uracil and 4-cyano-4"-ethynylbiphenyl, the CH hydrogen-bonding donors are sp2 and sp hybridized, respectively; a comparison of the calculated changes in 1H chemical shift with those for the sp3 hybridized CH donors in maltose (Yates et al.	Maltose	221-228	Sp3 transcription factor	Homo sapiens	193-196
18008022-0	2007	Amino acids that confer transport of raffinose and maltose sugars in the raffinose permease (RafB) of Escherichia coli as implicated by spontaneous mutations at Val-35, Ser-138, Ser-139, Gly-389 and Ile-391.	Maltose	51-58	hypothetical protein	Escherichia coli	93-97
18081283-3	2008	The maltose-mediated conformational changes within the MBP have been found to change the AFM-tip-protein interaction, therefore causing the frictional signal to change.	Maltose	4-11	myelin basic protein	Homo sapiens	55-58
18081283-6	2008	By measuring the change in the frictional force above the protein nanopatterns as a function of maltose concentration, we determined the dissociation constant for the MBP-cys-cys/maltose system to be kd = (1 +/- 0.04) microM.	Maltose	96-103	myelin basic protein	Homo sapiens	167-170
18081283-6	2008	By measuring the change in the frictional force above the protein nanopatterns as a function of maltose concentration, we determined the dissociation constant for the MBP-cys-cys/maltose system to be kd = (1 +/- 0.04) microM.	Maltose	179-186	myelin basic protein	Homo sapiens	167-170
18081283-7	2008	Our results show that the MBP-cys-cys system provides a very sensitive surface-based, protein nanobiosensor for maltose detection at the attogram level (approximately 100 nM concentration).	Maltose	112-119	myelin basic protein	Homo sapiens	26-29
17911381-4	2007	Allelic variation of the Tas1r3 gene influenced taste responsiveness to nonnutritive sweeteners (saccharin, acesulfame-K, sucralose, SC-45647), sugars (sucrose, maltose, glucose, fructose), sugar alcohols (erythritol, sorbitol), and some amino acids (D-tryptophan, D-phenylalanine, L-proline).	Maltose	161-168	taste receptor, type 1, member 3	Mus musculus	25-31
18008022-1	2007	In order to identify amino acid residues in the Escherichia coli raffinose-H(+) permease (RafB) that play a role in sugar selection and transport, we first incubated E. coli HS4006 containing plasmid pRU600 (expresses inducible raffinose permease and alpha-galactosidase) on maltose MacConkey indicator plates overnight.	Maltose	275-282	hypothetical protein	Escherichia coli	90-94
18008022-11	2007	The apparent K (i) value of maltose for RafB indicates a competitive relationship between maltose and raffinose.	Maltose	28-35	hypothetical protein	Escherichia coli	40-44
18008022-11	2007	The apparent K (i) value of maltose for RafB indicates a competitive relationship between maltose and raffinose.	Maltose	90-97	hypothetical protein	Escherichia coli	40-44
18008022-12	2007	Maltose "uphill" accumulation was greater for mutants (P <or= 0.05) than for cells with wild-type RafB.	Maltose	0-7	hypothetical protein	Escherichia coli	101-105
18008022-13	2007	Thus, we implicate residues in RafB that are responsible for raffinose transport and suggest that the substituted residues in RafB dictate structures that enhance transport of maltose.	Maltose	176-183	hypothetical protein	Escherichia coli	31-35
18008022-13	2007	Thus, we implicate residues in RafB that are responsible for raffinose transport and suggest that the substituted residues in RafB dictate structures that enhance transport of maltose.	Maltose	176-183	hypothetical protein	Escherichia coli	126-130
17915943-1	2007	In order to investigate the dynamic strength of the interaction between lung surfactant protein D (SP-D) and different sugars, maltose, mannose, glucose, and galactose, we have used an atomic force microscope to monitor the interaction on a single molecule scale.	Maltose	127-134	surfactant protein D	Homo sapiens	72-97
18189256-3	2008	With the mono-His6-tagged maltose binding protein (His6-MBP), thermodynamic modeling based on surface plasmon resonance (SPR) titration data showed that the MBP molecules in solution were linked, on average, to Ni.4 in 1:1 stoichiometry.	Maltose	26-33	myelin basic protein	Homo sapiens	56-59
18189256-3	2008	With the mono-His6-tagged maltose binding protein (His6-MBP), thermodynamic modeling based on surface plasmon resonance (SPR) titration data showed that the MBP molecules in solution were linked, on average, to Ni.4 in 1:1 stoichiometry.	Maltose	26-33	myelin basic protein	Homo sapiens	157-160
17961142-1	2007	The ATP binding cassette (ABC-) transporter mediating the uptake of maltose/maltodextrins in Escherichia coli/Salmonella enterica serovar Typhimurium is one of the best characterized systems and serves as a model for studying the molecular mechanism by which ABC importers exert their functions.	Maltose	68-75	ABC transporter	Escherichia coli	26-43
17915943-1	2007	In order to investigate the dynamic strength of the interaction between lung surfactant protein D (SP-D) and different sugars, maltose, mannose, glucose, and galactose, we have used an atomic force microscope to monitor the interaction on a single molecule scale.	Maltose	127-134	surfactant protein D	Homo sapiens	99-103
17915943-3	2007	Under these dynamic conditions, SP-D binds strongest to d-mannose and weakest to maltose and d-galactose.	Maltose	81-88	surfactant protein D	Homo sapiens	32-36
17915943-5	2007	On the basis of this finding, we propose that the binding of the disaccharide maltose to SP-D, which is energetically stronger than the binding of any of the monosacchrides, alters the structure of the binding site in a way that lowers the dynamic strength of the bond.	Maltose	78-85	surfactant protein D	Homo sapiens	89-93
17716624-1	2007	Human beta1-2N-acetylglucosaminyltransferase (hGnT1) lacking the first 103 amino acids was expressed as a maltose binding protein (MBP) fusion protein in inclusion bodies (IBs) in Escherichia coli and refolded using an oxido-shuffling method.	Maltose	106-113	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	46-51
17700863-2	2007	Use of the disaccharide maltose as the principal carbon source, in contrast to the preferred nutrient monosaccharide glucose, has been shown to induce a hyper-filamentous growth phenotype in a strain deficient for GPA2 which codes for a Galpha protein component that interacts with the glucose-sensing receptor Gpr1p to regulate filamentous growth.	Maltose	24-31	guanine nucleotide-binding protein subunit alpha	Saccharomyces cerevisiae S288C	214-218
17723085-4	2007	When some blood glucose monitoring systems are used--specifically, those that use test strips containing the enzymes glucose dehydrogenase-pyrroloquinolinequinone or glucose dye oxidoreductase--in patients receiving maltose, icodextrin, galactose, or xylose, interference of blood glucose levels can occur.	Maltose	216-223	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	Homo sapiens	117-138
17700863-2	2007	Use of the disaccharide maltose as the principal carbon source, in contrast to the preferred nutrient monosaccharide glucose, has been shown to induce a hyper-filamentous growth phenotype in a strain deficient for GPA2 which codes for a Galpha protein component that interacts with the glucose-sensing receptor Gpr1p to regulate filamentous growth.	Maltose	24-31	Gpr1p	Saccharomyces cerevisiae S288C	311-316
17700863-3	2007	In this report, we compare the global transcript and proteomic profiles of wild-type and Gpa2p deficient diploid yeast strains grown on both rich and nitrogen starved maltose media.	Maltose	167-174	guanine nucleotide-binding protein subunit alpha	Saccharomyces cerevisiae S288C	89-94
17715294-8	2007	We characterized the role of one Gr5a-related receptor, Gr64a, and found that it was required for the behavioral responses to glucose, sucrose, and maltose.	Maltose	148-155	Gustatory receptor 5a	Drosophila melanogaster	33-37
17715294-8	2007	We characterized the role of one Gr5a-related receptor, Gr64a, and found that it was required for the behavioral responses to glucose, sucrose, and maltose.	Maltose	148-155	Gustatory receptor 64a	Drosophila melanogaster	56-61
17559573-2	2007	Extracts of maltose/yeast extract/nitrate-grown cells contained all enzyme activities of a modified Embden-Meyerhof (EM) pathway, including ATP-dependent glucokinase, phosphoglucose isomerase, ATP-dependent 6-phosphofructokinase, fructose-1,6-phosphate aldolase, triose-phosphate isomerase, GAPOR, phosphoglycerate mutase, enolase and pyruvate kinase.	Maltose	12-19	phosphoglycerate mutase	Saccharomyces cerevisiae S288C	298-321
17629322-0	2007	How do trehalose, maltose, and sucrose influence some structural and dynamical properties of lysozyme? Insight from molecular dynamics simulations.	Maltose	18-25	lysozyme	Homo sapiens	93-102
17098455-9	2007	Substrate specificity for MG4 and MG6 indicated that the two enzymes are maltase-glucoamylases because they catalysed the hydrolysis of maltose and starch with alpha-1,4 and alpha-1,6 glycosidic bonds, but not sucrose with alpha-1,2 glycosidic bond which was hydrolyzed by sucrase-isomaltase.	Maltose	136-143	sucrase-isomaltase, intestinal	Camelus bactrianus	273-291
17400921-3	2007	We have previously created several heterotropic allosteric enzymes by recombining the genes for TEM1 beta-lactamase (BLA) and maltose binding protein (MBP) to create BLAs that are positively or negatively regulated by maltose.	Maltose	126-133	myelin basic protein	Homo sapiens	151-154
17192852-5	2007	We showed that Mal32 displayed on the cell surface of Saccharomyces cerevisiae laboratory strains was capable of hydrolysis of alpha-1,4-linkages, and that it increased the ability of a strain lacking a functional maltose permease to grow on maltotriose.	Maltose	214-221	alpha-glucosidase MAL32	Saccharomyces cerevisiae S288C	15-20
17098854-5	2007	AtSUC9 showed low substrate specificity, similar to AtSUC2 (At1g22710), and transported a wide range of glucosides, including helicin, salicin, arbutin, maltose, fraxin, esculin, turanose, and alpha-methyl-d-glucose.	Maltose	153-160	sucrose-proton symporter 9	Arabidopsis thaliana	0-6
16596410-4	2006	Using non-aqueous fractionation methods, we found that essentially all the maltose in mex1-1 leaves is located inside chloroplasts but only 40% of maltose in dpe2-1 leaves is located inside chloroplasts.	Maltose	75-82	root cap 1 (RCP1)	Arabidopsis thaliana	86-92
17177680-7	2006	This binding was saturable and was inhibited by the addition of maltose and ethylenediaminetetraacetic acid, suggesting the involvement of the carbohydrate recognition domain of SP-D.	Maltose	64-71	surfactant protein D	Homo sapiens	178-182
16980427-3	2006	Yeast strains deleted for SWD1, SWD3, SDC1, SET1, BRE2, or SPP1, encoding components of the COMPASS complex, fermented a medium containing 22% maltose with noticeably higher attenuation than did the wild type, resulting in production of up to 29% more ethanol.	Maltose	143-150	COMPASS subunit protein SWD1	Saccharomyces cerevisiae S288C	26-30
16980427-3	2006	Yeast strains deleted for SWD1, SWD3, SDC1, SET1, BRE2, or SPP1, encoding components of the COMPASS complex, fermented a medium containing 22% maltose with noticeably higher attenuation than did the wild type, resulting in production of up to 29% more ethanol.	Maltose	143-150	Sdc1p	Saccharomyces cerevisiae S288C	38-42
16980427-3	2006	Yeast strains deleted for SWD1, SWD3, SDC1, SET1, BRE2, or SPP1, encoding components of the COMPASS complex, fermented a medium containing 22% maltose with noticeably higher attenuation than did the wild type, resulting in production of up to 29% more ethanol.	Maltose	143-150	histone methyltransferase SET1	Saccharomyces cerevisiae S288C	44-48
16980427-3	2006	Yeast strains deleted for SWD1, SWD3, SDC1, SET1, BRE2, or SPP1, encoding components of the COMPASS complex, fermented a medium containing 22% maltose with noticeably higher attenuation than did the wild type, resulting in production of up to 29% more ethanol.	Maltose	143-150	Bre2p	Saccharomyces cerevisiae S288C	50-54
16980427-3	2006	Yeast strains deleted for SWD1, SWD3, SDC1, SET1, BRE2, or SPP1, encoding components of the COMPASS complex, fermented a medium containing 22% maltose with noticeably higher attenuation than did the wild type, resulting in production of up to 29% more ethanol.	Maltose	143-150	Spp1p	Saccharomyces cerevisiae S288C	59-63
16980427-6	2006	Deletion of SWD3 resulted in larger amounts of MAL12 transcript, encoding maltase, at the late stages of fermentation of 22% maltose.	Maltose	125-132	Swd3p	Saccharomyces cerevisiae S288C	12-16
16980427-6	2006	Deletion of SWD3 resulted in larger amounts of MAL12 transcript, encoding maltase, at the late stages of fermentation of 22% maltose.	Maltose	125-132	alpha-glucosidase MAL12	Saccharomyces cerevisiae S288C	47-52
16980562-4	2006	In this article, we measured the activities of recombinant DPE2 and AtPHS2 proteins with various substrates; we show that maltose and a highly branched, soluble heteroglycan (SHG) are excellent substrates for DPE2 and propose that a SHG is the in vivo substrate for DPE2 and AtPHS2.	Maltose	122-129	disproportionating enzyme 2	Arabidopsis thaliana	59-63
16980562-4	2006	In this article, we measured the activities of recombinant DPE2 and AtPHS2 proteins with various substrates; we show that maltose and a highly branched, soluble heteroglycan (SHG) are excellent substrates for DPE2 and propose that a SHG is the in vivo substrate for DPE2 and AtPHS2.	Maltose	122-129	alpha-glucan phosphorylase 2	Arabidopsis thaliana	68-74
16980562-4	2006	In this article, we measured the activities of recombinant DPE2 and AtPHS2 proteins with various substrates; we show that maltose and a highly branched, soluble heteroglycan (SHG) are excellent substrates for DPE2 and propose that a SHG is the in vivo substrate for DPE2 and AtPHS2.	Maltose	122-129	disproportionating enzyme 2	Arabidopsis thaliana	209-213
16980562-4	2006	In this article, we measured the activities of recombinant DPE2 and AtPHS2 proteins with various substrates; we show that maltose and a highly branched, soluble heteroglycan (SHG) are excellent substrates for DPE2 and propose that a SHG is the in vivo substrate for DPE2 and AtPHS2.	Maltose	122-129	disproportionating enzyme 2	Arabidopsis thaliana	209-213
16980562-4	2006	In this article, we measured the activities of recombinant DPE2 and AtPHS2 proteins with various substrates; we show that maltose and a highly branched, soluble heteroglycan (SHG) are excellent substrates for DPE2 and propose that a SHG is the in vivo substrate for DPE2 and AtPHS2.	Maltose	122-129	alpha-glucan phosphorylase 2	Arabidopsis thaliana	275-281
16980562-5	2006	In E. coli, MalQ and MalP preferentially use smaller maltodextrins (G(3)-G(7)) and we suggest that MalQ and DPE2 have similar, but nonidentical, roles in maltose metabolism.	Maltose	154-161	disproportionating enzyme 2	Arabidopsis thaliana	108-112
16980562-8	2006	The nighttime maltose level increased 4 times in the Atphs2-1 mutant.	Maltose	14-21	alpha-glucan phosphorylase 2	Arabidopsis thaliana	53-59
16980562-10	2006	Other plant species also contain SHG, DPE2, and alpha-glucan phosphorylase, so this pathway for maltose metabolism may be widespread among plants.	Maltose	96-103	disproportionating enzyme 2	Arabidopsis thaliana	38-42
16596410-5	2006	We found that maltose exists in a significant amount in the exudates collected from maltose-accumulating dpe2-1 Arabidopsis petioles.	Maltose	14-21	disproportionating enzyme 2	Arabidopsis thaliana	105-109
16596410-5	2006	We found that maltose exists in a significant amount in the exudates collected from maltose-accumulating dpe2-1 Arabidopsis petioles.	Maltose	84-91	disproportionating enzyme 2	Arabidopsis thaliana	105-109
16596410-6	2006	However, the amount of maltose in the exudates from mex1-1 petioles was not significantly different from that in wild-type phloem exudates.	Maltose	23-30	root cap 1 (RCP1)	Arabidopsis thaliana	52-58
16596410-7	2006	We found twice as much maltose in the roots of dpe2-1 plants relative to wild type but the maltose level in the roots of mex1-1 plants was not higher than wild type.	Maltose	23-30	disproportionating enzyme 2	Arabidopsis thaliana	47-51
16596410-7	2006	We found twice as much maltose in the roots of dpe2-1 plants relative to wild type but the maltose level in the roots of mex1-1 plants was not higher than wild type.	Maltose	91-98	root cap 1 (RCP1)	Arabidopsis thaliana	121-127
16596410-8	2006	We conclude that maltose accumulated in the cytosol of leaves can be carried from the shoots to the roots and that maltose accumulated in the chloroplast of mex1-1 leaves is not mobilized.	Maltose	115-122	root cap 1 (RCP1)	Arabidopsis thaliana	157-163
16596410-10	2006	The amount of maltose moved from the shoots to the roots increased in dpe2-1 plants.	Maltose	14-21	disproportionating enzyme 2	Arabidopsis thaliana	70-74
16596410-11	2006	The roots of dpe2-1 plants must have the capacity to metabolize the excess maltose.	Maltose	75-82	disproportionating enzyme 2	Arabidopsis thaliana	13-17
16527369-2	2006	The nsp4 proteinase was expressed either fused to maltose binding protein or carrying a C-terminal hexahistidine tag.	Maltose	50-57	serine protease 57	Homo sapiens	4-8
16527369-2	2006	The nsp4 proteinase was expressed either fused to maltose binding protein or carrying a C-terminal hexahistidine tag.	Maltose	50-57	endogenous retrovirus group K member 8, envelope	Homo sapiens	9-19
16797185-4	2006	Using several protein kinases as tests we found that amino-terminal fusion to maltose binding protein rescued expression of the poorly expressed human kinase Cot but had only a marginal effect on expression of a well-expressed kinase IKK-2.	Maltose	78-85	mitogen-activated protein kinase kinase kinase 8	Homo sapiens	158-161
16701074-4	2006	Recoveries of maltose from its o-substituted aniline (o-ABA, o-ABAD, and o-ABN) derivatives were 5-40%, but maltose was unrecoverable from AP and ANTS derivatives.	Maltose	14-21	hydroxysteroid 17-beta dehydrogenase 10	Homo sapiens	63-67
16797185-4	2006	Using several protein kinases as tests we found that amino-terminal fusion to maltose binding protein rescued expression of the poorly expressed human kinase Cot but had only a marginal effect on expression of a well-expressed kinase IKK-2.	Maltose	78-85	inhibitor of nuclear factor kappa B kinase subunit beta	Homo sapiens	234-239
16702880-0	2006	Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease.	Maltose	14-21	maltase-glucoamylase	Homo sapiens	52-72
16834772-2	2006	We have previously identified a genetic locus provisionally named bop that is involved in maltose metabolism and biofilm formation.	Maltose	90-97	SET and MYND domain containing 1	Mus musculus	66-69
16702880-0	2006	Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease.	Maltose	14-21	sucrase-isomaltase	Homo sapiens	99-116
16702880-1	2006	PURPOSE: The study"s purpose was to compare acarbose and maltose as inhibitors of maltase-glucoamylase activity for determining acid alpha-glucosidase activity in dried blood spot specimens for early identification of patients with infantile Pompe disease, a severe form of acid alpha-glucosidase deficiency.	Maltose	57-64	maltase-glucoamylase	Homo sapiens	82-102
16702880-3	2006	Acarbose or maltose was used to inhibit maltase-glucoamylase, an enzyme present in polymorphonuclear neutrophils that contributes to the total alpha-glucosidase activity at acidic pH.	Maltose	12-19	maltase-glucoamylase	Homo sapiens	40-60
16702880-3	2006	Acarbose or maltose was used to inhibit maltase-glucoamylase, an enzyme present in polymorphonuclear neutrophils that contributes to the total alpha-glucosidase activity at acidic pH.	Maltose	12-19	sucrase-isomaltase	Homo sapiens	143-160
16640603-1	2006	The recently characterized cytosolic transglucosidase DPE2 (EC 2.4.1.25) is essential for the cytosolic metabolism of maltose, an intermediate on the pathway by which starch is converted to sucrose at night.	Maltose	118-125	disproportionating enzyme 2	Arabidopsis thaliana	54-58
16536470-3	2006	Conjugation of the dyes to the S337C maltose binding protein (MBP) mutant provided conjugates of these dyes that are capable of detecting maltose with different sensitivities.	Maltose	37-44	myelin basic protein	Homo sapiens	62-65
16600035-5	2006	RESULTS: By exploiting a highly engineered bacterial strain, we expressed in soluble form the PLAC1-homology region of mammalian sperm receptor ZP3 as a fusion to maltose binding protein.	Maltose	163-170	placenta enriched 1	Homo sapiens	94-99
16600035-5	2006	RESULTS: By exploiting a highly engineered bacterial strain, we expressed in soluble form the PLAC1-homology region of mammalian sperm receptor ZP3 as a fusion to maltose binding protein.	Maltose	163-170	zona pellucida glycoprotein 3	Homo sapiens	144-147
16536470-4	2006	The dye INR gave a 3-fold (+200%) change in fluorescence intensity upon maltose binding when conjugated to S337C MBP with a binding constant (K(d)) of 435 microM.	Maltose	72-79	myelin basic protein	Homo sapiens	113-116
16384549-3	2006	Maltose binding to MBP is known to convert the open form of the protein to the closed form through conformational changes about the hinge region.	Maltose	0-7	myelin basic protein	Homo sapiens	19-22
16384549-5	2006	Hinge mutations that increased maltose affinity the most (and thus presumably close the apo-MBP domain the most) also abrogated switching the most.	Maltose	31-38	myelin basic protein	Homo sapiens	92-95
16297066-0	2005	RNA interference of Arabidopsis beta-amylase8 prevents maltose accumulation upon cold shock and increases sensitivity of PSII photochemical efficiency to freezing stress.	Maltose	55-62	chloroplast beta-amylase	Arabidopsis thaliana	32-45
16288781-2	2005	Zn(2+) binding by the engineered MBP was thought to require a large conformational change from "open" to "closed", similar to that observed when maltose is bound by the wild-type protein.	Maltose	145-152	myelin basic protein	Homo sapiens	33-36
16393328-4	2005	METHODS: Porcine SP-D was purified from bronchoalveolar lavage fluids of Lan-Yu mini-pigs, by affinity chromatography on maltose-sepharose.	Maltose	121-128	surfactant protein D	Sus scrofa	17-21
16440087-8	2006	Furthermore, the ability of these reagentless protein-nanoparticle assemblies to perform maltose biosensing reversibly is demonstrated with the addition of alpha-glucosidase.	Maltose	89-96	sucrase-isomaltase	Homo sapiens	156-173
16440087-9	2006	Three 50 microM maltose additions after alpha-glucosidase addition showed increases of 2.2 microM, 600 nM, and 150 nM maltose.	Maltose	16-23	sucrase-isomaltase	Homo sapiens	40-57
16440087-9	2006	Three 50 microM maltose additions after alpha-glucosidase addition showed increases of 2.2 microM, 600 nM, and 150 nM maltose.	Maltose	118-125	sucrase-isomaltase	Homo sapiens	40-57
16297066-4	2005	BMY8 RNAi lines with lower BMY8 expression exhibited a starch-excess phenotype, and a dramatic decrease in maltose accumulation during a 6-h cold shock at 4 degrees C. The decreased maltose content was also accompanied by decreased glucose, fructose and sucrose content in the BMY8 RNAi plants, consistent with the roles of beta-amylase and maltose in transitory starch metabolism.	Maltose	107-114	chloroplast beta-amylase	Arabidopsis thaliana	0-4
16297066-4	2005	BMY8 RNAi lines with lower BMY8 expression exhibited a starch-excess phenotype, and a dramatic decrease in maltose accumulation during a 6-h cold shock at 4 degrees C. The decreased maltose content was also accompanied by decreased glucose, fructose and sucrose content in the BMY8 RNAi plants, consistent with the roles of beta-amylase and maltose in transitory starch metabolism.	Maltose	182-189	chloroplast beta-amylase	Arabidopsis thaliana	0-4
16297066-4	2005	BMY8 RNAi lines with lower BMY8 expression exhibited a starch-excess phenotype, and a dramatic decrease in maltose accumulation during a 6-h cold shock at 4 degrees C. The decreased maltose content was also accompanied by decreased glucose, fructose and sucrose content in the BMY8 RNAi plants, consistent with the roles of beta-amylase and maltose in transitory starch metabolism.	Maltose	182-189	chloroplast beta-amylase	Arabidopsis thaliana	27-31
16297066-4	2005	BMY8 RNAi lines with lower BMY8 expression exhibited a starch-excess phenotype, and a dramatic decrease in maltose accumulation during a 6-h cold shock at 4 degrees C. The decreased maltose content was also accompanied by decreased glucose, fructose and sucrose content in the BMY8 RNAi plants, consistent with the roles of beta-amylase and maltose in transitory starch metabolism.	Maltose	182-189	chloroplast beta-amylase	Arabidopsis thaliana	27-31
16297066-4	2005	BMY8 RNAi lines with lower BMY8 expression exhibited a starch-excess phenotype, and a dramatic decrease in maltose accumulation during a 6-h cold shock at 4 degrees C. The decreased maltose content was also accompanied by decreased glucose, fructose and sucrose content in the BMY8 RNAi plants, consistent with the roles of beta-amylase and maltose in transitory starch metabolism.	Maltose	182-189	chloroplast beta-amylase	Arabidopsis thaliana	0-4
16297066-4	2005	BMY8 RNAi lines with lower BMY8 expression exhibited a starch-excess phenotype, and a dramatic decrease in maltose accumulation during a 6-h cold shock at 4 degrees C. The decreased maltose content was also accompanied by decreased glucose, fructose and sucrose content in the BMY8 RNAi plants, consistent with the roles of beta-amylase and maltose in transitory starch metabolism.	Maltose	182-189	chloroplast beta-amylase	Arabidopsis thaliana	27-31
16297066-4	2005	BMY8 RNAi lines with lower BMY8 expression exhibited a starch-excess phenotype, and a dramatic decrease in maltose accumulation during a 6-h cold shock at 4 degrees C. The decreased maltose content was also accompanied by decreased glucose, fructose and sucrose content in the BMY8 RNAi plants, consistent with the roles of beta-amylase and maltose in transitory starch metabolism.	Maltose	182-189	chloroplast beta-amylase	Arabidopsis thaliana	27-31
16297066-6	2005	Together, carbohydrate analysis and freezing stress results of BMY8 RNAi lines indicate that increased maltose content, by itself or together through a maltose-dependent increase in other soluble sugars, contributes to the protection of the photosynthetic electron transport chain during freezing stress.	Maltose	103-110	chloroplast beta-amylase	Arabidopsis thaliana	63-67
15982011-2	2005	SAMs presenting the disaccharide maltose as a neoglycoconjugate were produced, and the structure was studied by high resolution atomic force microscopy.	Maltose	33-40	methionine adenosyltransferase 1A	Homo sapiens	0-4
16243276-1	2005	Monolinoleoyl trehalose, maltose and cellobiose were synthesized by Candida antarctica lipase-catalyzed condensation in an organic solvent with a low water content.	Maltose	25-32	PAN0_003d1715	Moesziomyces antarcticus	87-93
16061816-2	2005	We demonstrate this approach by recombining the genes coding for TEM1 beta-lactamase (BLA) and the Escherichia coli maltose binding protein (MBP) to create a family of MBP-BLA hybrids in which maltose is a positive or negative effector of beta-lactam hydrolysis.	Maltose	116-123	beta-lactamase	Escherichia coli	172-175
16061816-2	2005	We demonstrate this approach by recombining the genes coding for TEM1 beta-lactamase (BLA) and the Escherichia coli maltose binding protein (MBP) to create a family of MBP-BLA hybrids in which maltose is a positive or negative effector of beta-lactam hydrolysis.	Maltose	193-200	TEM-1 beta-lactamase	Escherichia coli	65-84
16061816-2	2005	We demonstrate this approach by recombining the genes coding for TEM1 beta-lactamase (BLA) and the Escherichia coli maltose binding protein (MBP) to create a family of MBP-BLA hybrids in which maltose is a positive or negative effector of beta-lactam hydrolysis.	Maltose	193-200	beta-lactamase	Escherichia coli	86-89
16061816-2	2005	We demonstrate this approach by recombining the genes coding for TEM1 beta-lactamase (BLA) and the Escherichia coli maltose binding protein (MBP) to create a family of MBP-BLA hybrids in which maltose is a positive or negative effector of beta-lactam hydrolysis.	Maltose	193-200	beta-lactamase	Escherichia coli	172-175
16061816-3	2005	Some of these MBP-BLA switches were effectively "on-off" in nature, with maltose altering catalytic activity by as much as 600-fold.	Maltose	73-80	beta-lactamase	Escherichia coli	18-21
15950998-1	2005	Concatemers of various numbers of the third ligand binding repeat of human very-low density lipoprotein receptor arranged in tandem were fused to maltose-binding protein and expressed as soluble polypeptides.	Maltose	146-153	very low density lipoprotein receptor	Homo sapiens	75-112
15919894-1	2005	Like all 10 minor receptor group human rhinoviruses (HRVs), HRV23 and HRV25, previously classified as major group viruses, are neutralized by maltose binding protein (MBP)-V33333 (a soluble recombinant concatemer of five copies of repeat 3 of the very-low-density lipoprotein receptor fused to MBP), bind to low-density lipoprotein receptor in virus overlay blots, and replicate in intercellular adhesion molecule 1 (ICAM-1)-negative COS-7 cells.	Maltose	142-149	intercellular adhesion molecule 1	Homo sapiens	417-423
16851857-2	2005	Comparison of the vacuum and solution free energy surfaces for maltose shows the principal effects of water to be an increase in the rotational freedom of the alpha(1 --> 4) linkage brought about by lowering the energy barrier for syn to anti conformational changes as well as expansion of the range of low-energy phi,psi conformations.	Maltose	63-70	synemin	Homo sapiens	234-237
15591410-7	2005	Binding, aggregation, and enhancement of phagocytosis by recombinant rat SP-D was completely blocked by EDTA and inhibited by d-maltose and to a lesser extent by d-galactose, indicating the involvement of the carbohydrate recognition domain of SP-D in these functions.	Maltose	126-135	surfactant protein D	Rattus norvegicus	73-77
15973488-1	2005	Hydroquinone-alpha-glucoside was synthesised from hydroquinone and maltose as glucosyl donor by transglucosylation in a water system with alpha-glucosidase from baker"s yeast.	Maltose	67-74	sucrase-isomaltase	Homo sapiens	138-155
15802852-2	2005	The Zn(II) complex showed strong alpha-glucosidase inhibitory activity greater by about eighty times (substrate: maltose) and forty times (substrate: sucrose) compared with acarbose.	Maltose	113-120	sucrase isomaltase (alpha-glucosidase)	Mus musculus	33-50
15606797-4	2005	Porcine SP-D was purified from porcine bronchoalveolar lavage (BAL) by maltose-agarose and immunoglobulin M affinity chromatography.	Maltose	71-78	surfactant protein D	Homo sapiens	8-12
15698784-7	2005	Kinetic studies revealed that 16 inhibited both sucrose- and maltose-hydrolyzing activities of rat intestinal alpha-glucosidase uncompetitively.	Maltose	61-68	sucrase-isomaltase	Homo sapiens	110-127
15721779-7	2005	Briefly, recombinant wild-type PLB and SLN were over-produced in Escherichia coli as maltose binding protein fusion proteins.	Maltose	85-92	phospholamban	Homo sapiens	31-34
15721779-7	2005	Briefly, recombinant wild-type PLB and SLN were over-produced in Escherichia coli as maltose binding protein fusion proteins.	Maltose	85-92	sarcolipin	Homo sapiens	39-42
15777943-2	2005	In earlier studies we have demonstrated that the three monoclonal antibodies 39.4 (IgG2b), 39.5 (IgG2b) and 61.1(IgG3) bind weakly to the glycosidic alpha(1-4) bond present in e.g. maltose and panose.	Maltose	181-188	immunoglobulin heavy constant gamma 3 (G3m marker)	Homo sapiens	113-117
15552648-3	2004	The C. albicans erg27 strain was able to grow only in the presence of maltose indicating that the ERG27 gene is essential.	Maltose	70-77	3-keto-steroid reductase	Saccharomyces cerevisiae S288C	16-21
15590158-12	2005	In addition, 44%, 38%, and 8% of 5-HT-stimulated and 30%, 32%, and 5% of maltose-stimulated c-Fos-positive neurons exhibited, respectively, Glu, SP, and CGRP immunoreactivity.	Maltose	73-80	Fos proto-oncogene, AP-1 transcription factor subunit	Rattus norvegicus	92-97
15590158-12	2005	In addition, 44%, 38%, and 8% of 5-HT-stimulated and 30%, 32%, and 5% of maltose-stimulated c-Fos-positive neurons exhibited, respectively, Glu, SP, and CGRP immunoreactivity.	Maltose	73-80	calcitonin-related polypeptide alpha	Rattus norvegicus	153-157
15563967-7	2004	CE-L alleviated hyperglycemia caused by maltose or starch loading in normal and Streptozotocin (STZ)-induced diabetic mice with better efficacy than that of acarbose.	Maltose	40-47	carboxyl ester lipase	Mus musculus	0-4
15555998-2	2004	The gene encoding TEM1 beta-lactamase was circularly permuted in a random fashion and subsequently randomly inserted into the gene encoding Escherichia coli maltose binding protein.	Maltose	157-164	TEM-1 beta-lactamase	Escherichia coli	18-37
15552648-3	2004	The C. albicans erg27 strain was able to grow only in the presence of maltose indicating that the ERG27 gene is essential.	Maltose	70-77	3-keto-steroid reductase	Saccharomyces cerevisiae S288C	98-103
15308227-5	2004	alpha-Glucosidase hydrolyses maltose to alpha-D-glucose, which is converted to beta-D-glucose by mutarotase.	Maltose	29-36	sucrase-isomaltase	Homo sapiens	0-17
15016617-5	2004	Binding was inhibited with ethylenediamine tetraacetic acid and maltose, suggesting that the carbohydrate recognition domain of SP-D recognizes RSV glycoproteins in a calcium-dependent manner.	Maltose	64-71	surfactant associated protein D	Mus musculus	128-132
15313146-7	2004	The measurement of acid alpha-glucosidase activity with minimal interference by other alpha-glucosidases was accomplished using maltose as an inhibitor.	Maltose	128-135	sucrase-isomaltase	Homo sapiens	24-41
15228334-5	2004	As an alternative to surface immobilization, we have constructed a CaM/maltose binding protein fusion protein, which renders CaM translationally immobile in a low weight percent agarose gel.	Maltose	71-78	calmodulin 1	Homo sapiens	67-70
15228334-5	2004	As an alternative to surface immobilization, we have constructed a CaM/maltose binding protein fusion protein, which renders CaM translationally immobile in a low weight percent agarose gel.	Maltose	71-78	calmodulin 1	Homo sapiens	125-128
15220403-5	2004	Here, we found that LANA interacts with SUV39H1 histone methyltransferase, a key component of heterochromatin formation, as determined by use of a DNA pull-down assay with a biotinylated DNA fragment that contained a LANA-specific binding sequence and a maltose-binding protein pull-down assay.	Maltose	254-261	LANA	Human gammaherpesvirus 8	20-24
15220403-5	2004	Here, we found that LANA interacts with SUV39H1 histone methyltransferase, a key component of heterochromatin formation, as determined by use of a DNA pull-down assay with a biotinylated DNA fragment that contained a LANA-specific binding sequence and a maltose-binding protein pull-down assay.	Maltose	254-261	SUV39H1 histone lysine methyltransferase	Homo sapiens	40-47
14996213-2	2004	To investigate its fate in the cytosol, we characterised plants with mutations in a gene encoding a putative glucanotransferase (disproportionating enzyme; DPE2), a protein similar to the maltase Q (MalQ) gene product involved in maltose metabolism in bacteria.	Maltose	230-237	disproportionating enzyme 2	Arabidopsis thaliana	156-160
15134922-3	2004	We have expressed the N-terminal domain of ATP7B as a soluble C-terminal fusion with the maltose binding protein.	Maltose	89-96	ATPase copper transporting beta	Homo sapiens	43-48
15143436-7	2004	We develop here a hypothesis that starch degradation is closely sensed by hexokinase because a newly discovered pathway required for starch to sucrose conversion that involves maltose is one of few metabolic pathways that requires hexokinase activity.	Maltose	176-183	hexokinase 1	Homo sapiens	74-84
15143436-7	2004	We develop here a hypothesis that starch degradation is closely sensed by hexokinase because a newly discovered pathway required for starch to sucrose conversion that involves maltose is one of few metabolic pathways that requires hexokinase activity.	Maltose	176-183	hexokinase 1	Homo sapiens	231-241
15116434-12	2004	Interestingly, Mig1p also seems to mediate repression of FSY1 expression by high maltose concentrations.	Maltose	81-88	transcription factor MIG1	Saccharomyces cerevisiae S288C	15-20
15835162-2	2004	Raman spectra of collective OH stretching vibration of water molecules in aqueous solutions of maltose-pRX conjugates with different alpha-cyclodextrin (alpha-CD) threading on a poly(ethylene glycol) (PEG) chain was measured.	Maltose	95-102	periaxin	Homo sapiens	103-106
15835162-6	2004	It is suggested that rapid motion of maltose groups in the pRX conjugate can contribute to preserving ordered structure of the bulk water clusters.	Maltose	37-44	periaxin	Homo sapiens	59-62
14741221-7	2004	For one of these enzymes, the presence of maltose increased k(cat) by 70% and k(cat)/K(m) by 80% and resulted in kinetic parameters that were almost identical to TEM-1 beta-lactamase.	Maltose	42-49	TEM-1 beta-lactamase	Escherichia coli	162-182
14500708-0	2003	The Hsp90 molecular chaperone complex regulates maltose induction and stability of the Saccharomyces MAL gene transcription activator Mal63p.	Maltose	48-55	Hsp90 family chaperone HSC82	Saccharomyces cerevisiae S288C	4-9
14742512-3	2004	Full-length native SP-D aggregated pneumococci in a calcium-dependent manner that was inhibited by maltose acting as a competitive sugar.	Maltose	99-106	surfactant protein D	Homo sapiens	19-23
14500708-3	2003	Strains carrying mutations in genes encoding components of the Hsp90 chaperone complex, hsc82 Delta hsp82-T101I and hsc82 Delta cpr7 Delta, are defective for maltase induction and exhibit significantly reduced growth rates on media containing a limiting concentration of maltose (0.05%).	Maltose	271-278	Hsp90 family chaperone HSC82	Saccharomyces cerevisiae S288C	63-68
14500708-3	2003	Strains carrying mutations in genes encoding components of the Hsp90 chaperone complex, hsc82 Delta hsp82-T101I and hsc82 Delta cpr7 Delta, are defective for maltase induction and exhibit significantly reduced growth rates on media containing a limiting concentration of maltose (0.05%).	Maltose	271-278	Hsp90 family chaperone HSC82	Saccharomyces cerevisiae S288C	88-93
14500708-3	2003	Strains carrying mutations in genes encoding components of the Hsp90 chaperone complex, hsc82 Delta hsp82-T101I and hsc82 Delta cpr7 Delta, are defective for maltase induction and exhibit significantly reduced growth rates on media containing a limiting concentration of maltose (0.05%).	Maltose	271-278	Hsp90 family chaperone HSC82	Saccharomyces cerevisiae S288C	116-121
12730206-5	2003	Both native and recombinant decorin can bind to SP-D that is already bound to maltose-agarose matrix, and these SP-D-decorin complexes are dissociated at high salt (0.5-1.0 m NaCl) conditions, releasing the decorin.	Maltose	78-85	surfactant protein D	Homo sapiens	48-52
13129393-1	2003	A fluorescence resonance energy-transfer (FRET) sensing system for maltose based on E. coli maltose binding protein (MBP) is demonstrated.	Maltose	67-74	myelin basic protein	Homo sapiens	92-115
13129393-1	2003	A fluorescence resonance energy-transfer (FRET) sensing system for maltose based on E. coli maltose binding protein (MBP) is demonstrated.	Maltose	67-74	myelin basic protein	Homo sapiens	117-120
13129393-6	2003	In the use of these FRET pairs, MBP dissociation values for maltose were estimated (0.14-2.90 microM).	Maltose	60-67	myelin basic protein	Homo sapiens	32-35
12942071-7	2003	A second maltose sensor assembly consists of QDs coupled with Cy3-labelled MBP bound to beta-cyclodextrin-Cy3.5.	Maltose	9-16	myelin basic protein	Homo sapiens	75-78
12888356-3	2003	The high resolution crystal structures of maltose-bound rfhSP-D to 1.4A, and of rfhSP-D to 1.6A, define the fine detail of the mode and nature of carbohydrate recognition and provide insights into how a small fragment of human SP-D can bind to allergens/antigens or whole pathogens, and at the same time recruit and engage effector cells and molecules of humoral immunity.	Maltose	42-49	surfactant protein D	Homo sapiens	59-63
14593480-7	2004	Both dpe2-1 and dpe2-2 plants exhibited a dwarf phenotype and accumulated a large amount of maltose.	Maltose	92-99	disproportionating enzyme 2	Arabidopsis thaliana	5-9
14593480-7	2004	Both dpe2-1 and dpe2-2 plants exhibited a dwarf phenotype and accumulated a large amount of maltose.	Maltose	92-99	disproportionating enzyme 2	Arabidopsis thaliana	16-20
14593480-12	2004	As a result, dpe2 plants have higher maltose, higher starch, and higher maltodextrin but lower nighttime sucrose than wild-type plants.	Maltose	37-44	disproportionating enzyme 2	Arabidopsis thaliana	13-17
12794084-1	2003	The affinity of maltose-binding protein (MBP) for maltose and related carbohydrates was greatly increased by removal of groups in the interface opposite the ligand binding cleft.	Maltose	16-23	myelin basic protein	Homo sapiens	41-44
12716896-3	2003	Using proteolytic fragments and maltose-binding protein fusion proteins that together span full-length FN, we found DPPIV-binding sites in type III repeats 13, 14, and 15 (FNIII13, -14, and -15, respectively).	Maltose	32-39	dipeptidyl peptidase 4	Homo sapiens	116-121
12668681-5	2003	The synthetic peptides SCRQKSQPSE and SQVRESLLNL containing the protein kinase A motif for Ser31 and Ser251, respectively, within Opi1p were substrates for protein kinase A. Phosphorylation of S31A and S251A mutant maltose-binding protein-Opi1p fusion proteins by protein kinase A was reduced when compared with the wild type protein, and phosphopeptides present in wild type Opi1p were absent from the S31A and S251A mutant proteins.	Maltose	215-222	transcriptional regulator OPI1	Saccharomyces cerevisiae S288C	130-135
12668681-5	2003	The synthetic peptides SCRQKSQPSE and SQVRESLLNL containing the protein kinase A motif for Ser31 and Ser251, respectively, within Opi1p were substrates for protein kinase A. Phosphorylation of S31A and S251A mutant maltose-binding protein-Opi1p fusion proteins by protein kinase A was reduced when compared with the wild type protein, and phosphopeptides present in wild type Opi1p were absent from the S31A and S251A mutant proteins.	Maltose	215-222	transcriptional regulator OPI1	Saccharomyces cerevisiae S288C	239-244
12668681-5	2003	The synthetic peptides SCRQKSQPSE and SQVRESLLNL containing the protein kinase A motif for Ser31 and Ser251, respectively, within Opi1p were substrates for protein kinase A. Phosphorylation of S31A and S251A mutant maltose-binding protein-Opi1p fusion proteins by protein kinase A was reduced when compared with the wild type protein, and phosphopeptides present in wild type Opi1p were absent from the S31A and S251A mutant proteins.	Maltose	215-222	transcriptional regulator OPI1	Saccharomyces cerevisiae S288C	239-244
12475979-2	2003	We have generated constructs comprising the cytoplasmic segment of DEP-1 fused to the maltose-binding protein to identify potential substrates and thereby suggest a physiological function for DEP-1.	Maltose	86-93	protein tyrosine phosphatase receptor type J	Homo sapiens	192-197
12741813-8	2003	The conformation of the maltose molecules was similar to that of the condensation product of soybean beta-amylase, but differed from that of G5 in E172A.	Maltose	24-31	beta-amylase	Glycine max	101-113
12672526-3	2003	We demonstrate that a recombinant maltose binding protein fusion of Tc13 Tul (MBP-Tc13 Tul), a member of the T. cruzi antigen 13 family of surface antigen proteins, competes for binding sites with the beta-adrenergic receptor antagonist [125I]-CYP on membranes purified both from CHO cells expressing human beta(1)-ARs and from rat atria.	Maltose	34-41	myelin basic protein	Rattus norvegicus	78-81
12654004-5	2003	To address this, the NBDs of P-glycoprotein were expressed and purified to 95% homogeneity, as fusions to maltose-binding protein.	Maltose	106-113	ATP binding cassette subfamily B member 1	Homo sapiens	29-43
12714449-4	2003	The results are as follows: (i) when L-AP4 was mixed with one of the sweet substances, such as sucrose, glucose, fructose and maltose, large synergistic responses were observed.	Maltose	126-133	replication initiator 1	Rattus norvegicus	39-42
12573243-2	2003	This ChimMb, fused to the Maltose Binding Protein (MBP) and expressed in Escherichia coli as an apoprotein, binds protoheme in a 1:1 stoichiometric ratio.	Maltose	26-33	myelin basic protein	Physeter catodon	51-54
12413398-1	2003	A C-terminal portion of Ara12 subtilisin-like protease (residues 542-757) was expressed in Escherichia coli cells as a fusion protein bound to maltose binding protein.	Maltose	143-150	Subtilase family protein	Arabidopsis thaliana	24-29
12527799-4	2003	Three maltose binding protein-UGT2B7 fusion proteins, 2B7F3 and 2B7F4 incorporating the amino acids 24 to 118 and 24 to 96 of UGT2B7, respectively, and 2B7F5 incorporating amino acids 84 to 118 of UGT2B7 were expressed in Escherichia coli and purified by affinity chromatography.	Maltose	6-13	UDP glucuronosyltransferase family 2 member B7	Homo sapiens	30-36
12538894-0	2003	Insights into binding cooperativity of MATa1/MATalpha2 from the crystal structure of a MATa1 homeodomain-maltose binding protein chimera.	Maltose	105-112	homeodomain mating type protein alpha2	Saccharomyces cerevisiae S288C	45-54
12627496-7	2003	The ORF47 kinase phosphorylated maltose-binding protein, the mouse IgG2A heavy chain, the rabbit IgG heavy chain, casein, VZV ORF62, and VZV ORF63.	Maltose	32-39	tegument serine/threonine protein kinase	Human alphaherpesvirus 3	4-9
12627496-7	2003	The ORF47 kinase phosphorylated maltose-binding protein, the mouse IgG2A heavy chain, the rabbit IgG heavy chain, casein, VZV ORF62, and VZV ORF63.	Maltose	32-39	transcriptional regulator ICP4	Human alphaherpesvirus 3	126-131
12627496-7	2003	The ORF47 kinase phosphorylated maltose-binding protein, the mouse IgG2A heavy chain, the rabbit IgG heavy chain, casein, VZV ORF62, and VZV ORF63.	Maltose	32-39	regulatory protein ICP22	Human alphaherpesvirus 3	141-146
12450829-12	2002	In the presence of both maltose and fructose in the medium, induction of hexokinase activity occurred in all sourdough LAB species mentioned above, explaining why no glucose accumulation was found extracellularly.	Maltose	24-31	hexokinase-6	Triticum aestivum	73-83
12230479-17	2002	In addition, some diffusion of maltose (DP2) from blood to dialysate may have occurred.	Maltose	31-38	transcription factor Dp-2	Homo sapiens	40-43
12624429-4	2002	Invertase, maltase, and lactase activities were measured by monitoring the conversion of [U-(14)C]sucrose, [U-(14)C]maltose, and [D-[1-(14)C]glucose] lactose to radioactive hexoses, which were phosphorylated in the presence of adenosine triphosphatase and yeast hexokinase and then separated from their precursor by ion-exchange chromatography.	Maltose	116-123	lactase	Rattus norvegicus	24-31
12406721-6	2002	By complementing this strain with permeases encoded by MAL31, MAL61, and AGT1, it was possible to measure their specific transport kinetics by using maltotriose and maltose.	Maltose	165-172	maltose permease	Saccharomyces cerevisiae S288C	55-60
12406721-6	2002	By complementing this strain with permeases encoded by MAL31, MAL61, and AGT1, it was possible to measure their specific transport kinetics by using maltotriose and maltose.	Maltose	165-172	alpha-glucoside permease	Saccharomyces cerevisiae S288C	73-77
12406721-8	2002	Maltotriose utilization from the permease encoded by AGT1 was regulated by the same genetic mechanisms as those involving the maltose transcriptional activator.	Maltose	126-133	alpha-glucoside permease	Saccharomyces cerevisiae S288C	53-57
12406721-9	2002	Competition studies carried out with two industrial strains, one not containing any homologue of AGT1, showed that maltose uptake and maltotriose uptake were competitive and that maltose was the preferred substrate.	Maltose	115-122	alpha-glucoside permease	Saccharomyces cerevisiae S288C	97-101
12406721-9	2002	Competition studies carried out with two industrial strains, one not containing any homologue of AGT1, showed that maltose uptake and maltotriose uptake were competitive and that maltose was the preferred substrate.	Maltose	179-186	alpha-glucoside permease	Saccharomyces cerevisiae S288C	97-101
12506981-3	2002	Maltose and other oligosaccharides were less preferentially hydrolyzed and were used as a glucosyl donor for transglucosylation by the enzyme, demonstrating distinct substrate specificity as a fungal alpha-glucosidase.	Maltose	0-7	sucrase-isomaltase	Homo sapiens	200-217
12530690-6	2002	To understand the cell biology and function of mammalian peroxisomal ABC transporters and to determine their role in the pathogenesis of X-ALD we developed a system for expressing functional ABC protein domains in fusion with the maltose binding protein.	Maltose	230-237	ATP binding cassette subfamily B member 6 (Langereis blood group)	Homo sapiens	69-72
12185084-1	2002	LamB (maltoporin) is essential for the uptake of maltose and malto-oligosaccharides across the outer membrane of Escherichia coli.	Maltose	49-56	maltoporin	Escherichia coli	6-16
12237104-6	2002	When fused to GST, maltose-binding protein, or the WAVE1 proline-rich domain, N-WASP VCA and WAVE1 VCA mutant proteins with two V motifs showed stronger activities than wild-type WAVE1 VCA with one V motif, demonstrating the importance of two V motifs for strong VCA activity.	Maltose	19-26	WASP like actin nucleation promoting factor	Homo sapiens	78-84
11916969-6	2002	Mannose, glucose, maltose, and inositol, at millimolar concentrations, competed for human SP-D binding to the bacterial membrane.	Maltose	18-25	surfactant protein D	Homo sapiens	90-94
12368358-2	2002	Using random mutagenesis of a chimera of maltose-binding protein and LEL residues 113 to 201, we have determined that the E2-binding site on CD81 comprises residues Ile(182), Phe(186), Asn(184), and Leu(162).	Maltose	41-48	CD81 molecule	Homo sapiens	141-145
12122147-8	2002	SGLT1 activity is paradoxically higher for mice consuming sucrose than for mice consuming maltose, despite maltose hydrolysis yielding double the glucose load yielded by sucrose hydrolysis, and despite glucose constituting the load upon SGLT1.	Maltose	90-97	solute carrier family 5 (sodium/glucose cotransporter), member 1	Mus musculus	0-5
12122147-8	2002	SGLT1 activity is paradoxically higher for mice consuming sucrose than for mice consuming maltose, despite maltose hydrolysis yielding double the glucose load yielded by sucrose hydrolysis, and despite glucose constituting the load upon SGLT1.	Maltose	107-114	solute carrier family 5 (sodium/glucose cotransporter), member 1	Mus musculus	0-5
12135486-4	2002	The isolated NBDs of MRP1 have been characterized in Escherichia coli as fusions with either the glutathione-S-transferase (GST) or the maltose-binding domain (MBP).	Maltose	136-143	ATP binding cassette subfamily C member 1	Homo sapiens	21-25
12469296-5	2002	The recombinant strain expressed more than 700-fold of the beta-gal activity as compared to the wild type strain under induction by maltose.	Maltose	132-139	hypothetical protein	Aspergillus oryzae RIB40	59-67
11880626-4	2002	We have shown that maltose-binding fusion proteins (MBP) containing the COOH termini of K(ATP) channels (Kir1.1, Kir6.1, and Kir6.2) form functional tetramers that directly bind at least two ATP molecules with negative cooperativity.	Maltose	19-26	potassium inwardly rectifying channel subfamily J member 1	Homo sapiens	105-111
11880626-4	2002	We have shown that maltose-binding fusion proteins (MBP) containing the COOH termini of K(ATP) channels (Kir1.1, Kir6.1, and Kir6.2) form functional tetramers that directly bind at least two ATP molecules with negative cooperativity.	Maltose	19-26	potassium inwardly rectifying channel subfamily J member 8	Homo sapiens	113-119
11880626-4	2002	We have shown that maltose-binding fusion proteins (MBP) containing the COOH termini of K(ATP) channels (Kir1.1, Kir6.1, and Kir6.2) form functional tetramers that directly bind at least two ATP molecules with negative cooperativity.	Maltose	19-26	potassium inwardly rectifying channel subfamily J member 11	Homo sapiens	125-131
11856348-3	2002	PknA fused to maltose-binding protein was expressed in Escherichia coli; it exhibited a molecular mass of approximately 97 kDa.	Maltose	14-21	serine/threonine-protein kinase PknA	Mycobacterium tuberculosis H37Rv	0-4
11136464-5	2001	The closest homologues of sut1+ are the sucrose uptake transporters (SUTs) from higher plants that transport sucrose with a higher affinity than maltose.	Maltose	145-152	Sut1p	Saccharomyces cerevisiae S288C	26-30
11682185-4	2001	The transcription of the yopH gene for YopH phosphatase in these maltose mutants was unchanged and revealed a maltose mutation impaired in the secretion of Yop proteins instead of their expression.	Maltose	65-72	yopH	Yersinia enterocolitica	25-29
11682185-4	2001	The transcription of the yopH gene for YopH phosphatase in these maltose mutants was unchanged and revealed a maltose mutation impaired in the secretion of Yop proteins instead of their expression.	Maltose	65-72	yopH	Yersinia enterocolitica	39-43
11682185-4	2001	The transcription of the yopH gene for YopH phosphatase in these maltose mutants was unchanged and revealed a maltose mutation impaired in the secretion of Yop proteins instead of their expression.	Maltose	110-117	yopH	Yersinia enterocolitica	25-29
11682185-4	2001	The transcription of the yopH gene for YopH phosphatase in these maltose mutants was unchanged and revealed a maltose mutation impaired in the secretion of Yop proteins instead of their expression.	Maltose	110-117	yopH	Yersinia enterocolitica	39-43
11466318-3	2001	To determine DNA binding domain of Rme1p, a series of Rme1p derivatives fused with maltose-binding protein were purified and characterized by gel mobility shift assay.	Maltose	83-90	Rme1p	Saccharomyces cerevisiae S288C	35-40
11481673-2	2001	This paper reports on physiological studies on the hxk2 deletion strain on mixtures of glucose/sucrose, glucose/galactose, glucose/maltose and glucose/ethanol in aerobic batch cultures.	Maltose	131-138	hexokinase 2	Saccharomyces cerevisiae S288C	51-55
11353807-4	2001	Two maltose binding protein fusion proteins, 2B7F1 and 2B7F2, incorporating the first 157 or 119 amino acids, respectively, of UGT2B7 were expressed in Escherichia coli and purified by affinity chromatography.	Maltose	4-11	UDP glucuronosyltransferase family 2 member B7	Homo sapiens	127-133
11409176-3	2001	HSP12 and HSP104 were transcribed 10 h earlier with maltose than with glucose.	Maltose	52-59	lipid-binding protein HSP12	Saccharomyces cerevisiae S288C	0-5
11409176-3	2001	HSP12 and HSP104 were transcribed 10 h earlier with maltose than with glucose.	Maltose	52-59	chaperone ATPase HSP104	Saccharomyces cerevisiae S288C	10-16
11409176-6	2001	Thus, the HSP26 and the HSP30 promoter can be used for late, phase-specific expression of the desired genes with glucose or maltose as carbon source, and HSP12 with glucose only.	Maltose	124-131	chaperone protein HSP26	Saccharomyces cerevisiae S288C	10-15
11409176-6	2001	Thus, the HSP26 and the HSP30 promoter can be used for late, phase-specific expression of the desired genes with glucose or maltose as carbon source, and HSP12 with glucose only.	Maltose	124-131	Hsp30p	Saccharomyces cerevisiae S288C	24-29
11119485-4	2001	These effects are calcium dependent and inhibited with maltose but not lactose, consistent with involvement of the SP-D carbohydrate recognition domain.	Maltose	55-62	surfactant protein D	Rattus norvegicus	115-119
12702465-5	2001	On the other hand, the alpha-glucoside permease encoded by the AGT1 gene had a high affinity (K(m) approximately 7 mM) for trehalose, a low affinity (K(m) approximately 18 mM) for maltose and maltotriose, and a very low affinity (K(m) approximately 35 mM) for alpha-methylglucoside.	Maltose	180-187	alpha-glucoside permease	Saccharomyces cerevisiae S288C	63-67
11272834-1	2001	The sfsA gene was identified as one of the sfs genes the over-expression of which stimulates maltose fermentation of the Mal- Escherichia coli strain MK2001 (crp*1, cya:Km(r)).	Maltose	93-100	cysteine-rich protein 1 (intestinal)	Mus musculus	158-163
11136464-7	2001	Sut1p was found to transport maltose with a Km of 6.5 +/- 0.4 mM and sucrose with a Km of 36.3 +/- 9.7 mM.	Maltose	29-36	Sut1p	Saccharomyces cerevisiae S288C	0-5
11136464-9	2001	Glucose repression of sut1+ at the transcriptional level is also consistent with a physiological function for Sut1p in maltose uptake.	Maltose	119-126	Sut1p	Saccharomyces cerevisiae S288C	22-26
11136464-9	2001	Glucose repression of sut1+ at the transcriptional level is also consistent with a physiological function for Sut1p in maltose uptake.	Maltose	119-126	Sut1p	Saccharomyces cerevisiae S288C	110-115
10769203-4	2000	Using maltose binding protein fusion constructs to the carboxy-terminal domains of utrophin we were able to demonstrate specific interactions between the WW, EF and ZZ domains of utrophin and (beta)-dystroglycan by co-immunoprecipitation with endogenous (beta)-dystroglycan.	Maltose	6-13	utrophin	Homo sapiens	83-91
11063508-3	2000	In this study, recombinant HIV-1 p51 and p66 with Ser-Ser at the N termini (Ser-Ser-rp51 and Ser-Ser-rp66) were produced in E. coli as fusion proteins with maltose binding protein containing a factor Xa site between the two proteins and were purified after digestion with factor Xa.	Maltose	156-163	tetratricopeptide repeat domain 8	Homo sapiens	84-88
11049744-6	2000	The full-length NS4A fused to the maltose binding protein is soluble and maintains its NS3 protease-enhancing activity.	Maltose	34-41	KRAS proto-oncogene, GTPase	Homo sapiens	87-90
11103228-4	2000	Salivary alpha-amylase rapidly degraded the oligosaccharides (degree of polymerisation > 3), mainly to maltose and maltotriose.	Maltose	106-113	amylase alpha 1A	Homo sapiens	0-22
10891347-1	2000	The His(6)-tagged N- and C-terminal nucleotide binding (ATP Binding Cassette, ABC) domains of the human multidrug resistance associated protein, MRP1, were expressed in bacteria in fusion to the bacterial maltose binding protein and a two-step affinity purification was utilized.	Maltose	205-212	ATP binding cassette subfamily C member 3	Homo sapiens	104-143
10891347-1	2000	The His(6)-tagged N- and C-terminal nucleotide binding (ATP Binding Cassette, ABC) domains of the human multidrug resistance associated protein, MRP1, were expressed in bacteria in fusion to the bacterial maltose binding protein and a two-step affinity purification was utilized.	Maltose	205-212	ATP binding cassette subfamily C member 1	Homo sapiens	145-149
11123337-5	2001	Here, we report expression of an in-frame fusion of a trimerizing neck region of surfactant protein D with the globular head region of C1q B chain as a fusion to Escherichia coli maltose binding protein.	Maltose	179-186	complement C1q A chain	Homo sapiens	135-138
10873783-9	2000	In addition, nuclear transport of a maltose binding protein-fusion protein containing the C-terminal NLS of the U27 protein was inhibited by both wheat germ agglutinin and a Q69L Ran-GTP mutant, indicating that the U27 protein is transported into the nucleus from the cytoplasm by means of classic nuclear transport machinery.	Maltose	36-43	DNA polymerase processivity subunit	Human betaherpesvirus 7	112-115
10873783-9	2000	In addition, nuclear transport of a maltose binding protein-fusion protein containing the C-terminal NLS of the U27 protein was inhibited by both wheat germ agglutinin and a Q69L Ran-GTP mutant, indicating that the U27 protein is transported into the nucleus from the cytoplasm by means of classic nuclear transport machinery.	Maltose	36-43	DNA polymerase processivity subunit	Human betaherpesvirus 7	215-218
10856318-6	2000	Rat bronchoalveolar lavage (BAL) fluid was enriched for surfactant protein D (SP-D) using maltose agarose affinity chromatography.	Maltose	90-97	surfactant protein D	Rattus norvegicus	56-76
10856318-6	2000	Rat bronchoalveolar lavage (BAL) fluid was enriched for surfactant protein D (SP-D) using maltose agarose affinity chromatography.	Maltose	90-97	surfactant protein D	Rattus norvegicus	78-82
10903030-3	2000	In this work we examine the solution behavior of the beta anomer of maltose and cyclohexa-, cyclohepta-, and cyclooctaamyloses (alpha-, beta-, and gamma-cyclodextrins or alpha-, beta-, and gamma-CDs, respectively), as well as of two larger (DP 10, epsilon-CD; DP 21) cyclomaltooligosaccharides, CA10 and CA21.	Maltose	68-75	carbonic anhydrase 10	Homo sapiens	295-299
10848977-4	2000	We expressed vIL-6 in Escherichia coli as a fusion protein with recombinant periplasmic maltose binding protein.	Maltose	88-95	K2	Human gammaherpesvirus 8	13-18
10848977-5	2000	After cleavage from the maltose binding protein moiety and purification, vIL-6 was shown to be correctly folded using circular dichroism spectroscopy.	Maltose	24-31	K2	Human gammaherpesvirus 8	73-78
10848986-8	2000	These aptamers bind to DeltaNS3 with a binding constant of about 10 nM and inhibit approximately 90% of the protease activity of DeltaNS3 and MBP-NS3 (full-length of NS3 fused with maltose binding protein).	Maltose	181-188	KRAS proto-oncogene, GTPase	Homo sapiens	28-31
10769203-4	2000	Using maltose binding protein fusion constructs to the carboxy-terminal domains of utrophin we were able to demonstrate specific interactions between the WW, EF and ZZ domains of utrophin and (beta)-dystroglycan by co-immunoprecipitation with endogenous (beta)-dystroglycan.	Maltose	6-13	utrophin	Homo sapiens	179-187
10769052-1	2000	We raised a polyclonal antibody against maltose binding protein fusion human cGMP-binding, cGMP-specific phosphodiesterase (PDE5) produced in E. coli.	Maltose	40-47	phosphodiesterase 5A	Homo sapiens	124-128
10791714-4	2000	Deletion of this gene in a MAL+ tps1 mutant abolished trehalose accumulation on a maltose or galactose mineral medium.	Maltose	82-89	alpha,alpha-trehalose-phosphate synthase (UDP-forming) TPS1	Saccharomyces cerevisiae S288C	32-36
10906770-3	2000	Second, rp66 with Ser-Ser at the N-terminus was produced as a fusion protein with maltose-binding protein containing a factor Xa site between the two proteins (MBP-Ser-Ser-rp66) and was released from the fusion protein by factor Xa (Ser-Ser-rp66).	Maltose	82-89	retinol binding protein 3	Homo sapiens	8-12
10821175-2	2000	Loss of REG1 relieves glucose repression of many genes, including the MAL structural genes that encode the maltose fermentation enzymes.	Maltose	107-114	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	8-12
10821175-7	2000	Loss of Reg2p modestly reduces the rates of both glucose-induced proteolysis of maltose permease and inactivation of maltose transport activity.	Maltose	80-87	protein phosphatase regulator REG2	Saccharomyces cerevisiae S288C	8-13
10821175-8	2000	Overexpression of Reg2p in a reg1delta strain suppresses the effect on maltose permease proteolysis and partially restores the inactivation of maltose transport activity, but does not affect the insensitivity of MAL gene expression to repression by glucose observed in this strain.	Maltose	71-78	protein phosphatase regulator REG2	Saccharomyces cerevisiae S288C	18-23
10821175-8	2000	Overexpression of Reg2p in a reg1delta strain suppresses the effect on maltose permease proteolysis and partially restores the inactivation of maltose transport activity, but does not affect the insensitivity of MAL gene expression to repression by glucose observed in this strain.	Maltose	143-150	protein phosphatase regulator REG2	Saccharomyces cerevisiae S288C	18-23
10821175-9	2000	Thus, protein phosphatase type-1 (Glc7p-Reglp and Glc7p-Reg2p) plays a role in transduction of the glucose signal during glucose-induced proteolysis of maltose permease, but only Glc7p-Reglp is involved in glucose-induced inactivation of maltose transport activity and glucose repression of MAL gene expression.	Maltose	152-159	protein phosphatase regulator REG2	Saccharomyces cerevisiae S288C	56-61
10821175-9	2000	Thus, protein phosphatase type-1 (Glc7p-Reglp and Glc7p-Reg2p) plays a role in transduction of the glucose signal during glucose-induced proteolysis of maltose permease, but only Glc7p-Reglp is involved in glucose-induced inactivation of maltose transport activity and glucose repression of MAL gene expression.	Maltose	238-245	protein phosphatase regulator REG2	Saccharomyces cerevisiae S288C	56-61
10821175-10	2000	Overexpression of REG1 partially restores proteolysis of maltose permease in a grr1delta strain, which lacks glucose signaling, but does not rescue rapid inactivation of maltose transport activity or sensitivity to glucose repression.	Maltose	57-64	protein phosphatase regulator REG1	Saccharomyces cerevisiae S288C	18-22
10719169-1	2000	The proteinase of bovine leukemia virus (BLV) was cloned into pMal-c2 vector with N-terminal or with N- as well as C-terminal flanking sequences, and expressed in fusion with maltose binding protein.	Maltose	175-182	endogenous retrovirus group K member 18	Homo sapiens	4-14
10648165-7	2000	The optimal pH for the hydrolysis of maltose by recombinant alpha-glucosidase is between 3.5 and 4.5.	Maltose	37-44	Agl1	Hordeum vulgare	60-77
10628974-4	2000	Glucose also blocks MAL-activator-mediated maltose induction through a Mig1p-independent mechanism that we refer to as glucose inhibition.	Maltose	43-50	transcription factor MIG1	Saccharomyces cerevisiae S288C	71-76
10906770-3	2000	Second, rp66 with Ser-Ser at the N-terminus was produced as a fusion protein with maltose-binding protein containing a factor Xa site between the two proteins (MBP-Ser-Ser-rp66) and was released from the fusion protein by factor Xa (Ser-Ser-rp66).	Maltose	82-89	coagulation factor X	Homo sapiens	119-128
10906770-3	2000	Second, rp66 with Ser-Ser at the N-terminus was produced as a fusion protein with maltose-binding protein containing a factor Xa site between the two proteins (MBP-Ser-Ser-rp66) and was released from the fusion protein by factor Xa (Ser-Ser-rp66).	Maltose	82-89	myelin basic protein	Homo sapiens	160-163
10561588-3	1999	Upon binding of maltose, MBP undergoes a large structural change that closes the binding cleft, i.e. the distance between its two domains decreases.	Maltose	16-23	myelin basic protein	Homo sapiens	25-28
10527944-1	1999	Human and bovine surfactant proteins D (SP-D) were purified from late amniotic fluid and bronchioalveolar lavage on the basis of its Ca(2+)-dependent affinity for maltose.	Maltose	163-170	pulmonary surfactant-associated protein D	Bos taurus	17-38
10527944-1	1999	Human and bovine surfactant proteins D (SP-D) were purified from late amniotic fluid and bronchioalveolar lavage on the basis of its Ca(2+)-dependent affinity for maltose.	Maltose	163-170	pulmonary surfactant-associated protein D	Bos taurus	40-44
10482574-3	1999	In the present study, we further characterized the AAV Rep68/78 helicase, ATPase, and endonuclease activities by using a maltose binding protein-Rep68 fusion (MBP-Rep68Delta) produced in Escherichia coli cells and Rep78 produced in vitro in a rabbit reticulocyte lysate system.	Maltose	121-128	helicase for meiosis 1	Homo sapiens	64-72
10482574-3	1999	In the present study, we further characterized the AAV Rep68/78 helicase, ATPase, and endonuclease activities by using a maltose binding protein-Rep68 fusion (MBP-Rep68Delta) produced in Escherichia coli cells and Rep78 produced in vitro in a rabbit reticulocyte lysate system.	Maltose	121-128	ATPase	Escherichia coli	74-80
10482574-3	1999	In the present study, we further characterized the AAV Rep68/78 helicase, ATPase, and endonuclease activities by using a maltose binding protein-Rep68 fusion (MBP-Rep68Delta) produced in Escherichia coli cells and Rep78 produced in vitro in a rabbit reticulocyte lysate system.	Maltose	121-128	myelin basic protein	Homo sapiens	159-162
10589015-5	1999	One isoform (GmPRO1) with a length of 394 bp corresponding to 131 amino acid residues was subcloned and expressed in fusion with the maltose-binding protein.	Maltose	133-140	profilin-2	Glycine max	13-19
10589015-6	1999	Moreover, 3 overlapping recombinant soybean profilin fragments comprising amino acid residues 1-65, 38-88, and 50-131 were also prepared as maltose-binding protein fusion proteins.	Maltose	140-147	profilin	Glycine max	44-52
10542261-8	1999	MFAP4 also showed calcium-dependent binding to mannan, which was partially inhibited by maltose.	Maltose	88-95	microfibril associated protein 4	Bos taurus	0-5
10449801-1	1999	The mechanism of the protochlorophyllide (PChlide) photoreduction reaction operating in light-adapted plants and catalyzed by NADPH:protochlorophyllide oxidoreductase B (PORb) has been analyzed by low-temperature fluorescence spectroscopy by using purified barley PORb overexpressed heterologously in Escherichia coli as a fusion protein with the maltose-binding protein.	Maltose	347-354	PorB	Hordeum vulgare	126-168
10456901-3	1999	Rat SP-D but not rat SP-A bound the conidia, and the binding was inhibited by EDTA, mannose, glucose, maltose, and inositol.	Maltose	102-109	surfactant protein D	Rattus norvegicus	4-8
10449801-1	1999	The mechanism of the protochlorophyllide (PChlide) photoreduction reaction operating in light-adapted plants and catalyzed by NADPH:protochlorophyllide oxidoreductase B (PORb) has been analyzed by low-temperature fluorescence spectroscopy by using purified barley PORb overexpressed heterologously in Escherichia coli as a fusion protein with the maltose-binding protein.	Maltose	347-354	PorB	Hordeum vulgare	170-174
9888983-1	1999	AB982793 "The maltose-binding protein as a scaffold for monovalent display of peptides derived from phage Libraries," by michael B. Zwick, lori L. C. Bonnycastle, karen A. Noren, sara venturini, edward leong, carlos F. Barbas, III, christopher J. Noren, and jamie K. Scott, pages 87-97:	Maltose	14-21	secretion associated Ras related GTPase 1A	Homo sapiens	179-183
10085129-5	1999	Maltose-binding protein caveolin and glutathione S-transferase-GRK fusion proteins were used to map overlapping regions in the N termini of both GRK2 and GRK5 that appear to mediate conserved GRK/caveolin interactions.	Maltose	0-7	G protein-coupled receptor kinase 2	Mus musculus	145-149
10085129-5	1999	Maltose-binding protein caveolin and glutathione S-transferase-GRK fusion proteins were used to map overlapping regions in the N termini of both GRK2 and GRK5 that appear to mediate conserved GRK/caveolin interactions.	Maltose	0-7	G protein-coupled receptor kinase 5	Mus musculus	154-158
10085129-5	1999	Maltose-binding protein caveolin and glutathione S-transferase-GRK fusion proteins were used to map overlapping regions in the N termini of both GRK2 and GRK5 that appear to mediate conserved GRK/caveolin interactions.	Maltose	0-7	G protein-coupled receptor kinase 4	Mus musculus	145-148
10350483-7	1999	Low concentrations of maltose, D-glucose, 3-O-methylglucose, and other GLUT1 import-site reactive sugars increase k-1(app) and reduce k1(app) for cytochalasin B interaction with GLUT1.	Maltose	22-29	solute carrier family 2 member 1	Homo sapiens	178-183
10085158-4	1999	In order to clarify the mechanism by which the Vpr accessory protein is trans-incorporated into progeny virion particles, we tested whether HIV-1 Vpr interacted with the Pr55(gag) using the yeast two-hybrid system and the maltose-binding protein pull-down assay.	Maltose	222-229	Vpr	Human immunodeficiency virus 1	47-50
10603170-7	1999	The SVV UDG is enzymatically active as determined by the ability of a SVV UDG-maltose binding protein fusion construct to remove [(3)H]-uracil incorporated into DNA.	Maltose	78-85	uracil DNA glycosylase	Homo sapiens	8-11
10603170-7	1999	The SVV UDG is enzymatically active as determined by the ability of a SVV UDG-maltose binding protein fusion construct to remove [(3)H]-uracil incorporated into DNA.	Maltose	78-85	uracil DNA glycosylase	Homo sapiens	74-77
9919658-1	1999	The AGT1 permease is a alpha-glucoside-H+ symporter responsible for the active transport of maltose, trehalose, maltotriose, alpha-methylglucoside, melezitose and sucrose.	Maltose	92-99	alpha-glucoside permease	Saccharomyces cerevisiae S288C	4-8
10599864-2	1999	Wild-type and N-terminal 35-, 38-, and 44-amino acid-deleted mutants of human tyrosine hydroxylase type 1 (hTH1) fused to maltose-binding protein via the target sequence for a restriction protease were expressed in Escherichia coli and purified.	Maltose	122-129	negative elongation factor complex member C/D	Homo sapiens	107-111
9799229-7	1998	Using epitope tags, antibodies and maltose-binding protein markers, we find that the helical domains of Sso, Snc and both halves of Sec9 are all aligned in parallel within the SNARE complex, suggesting that the yeast exocytic SNARE complex consists of a parallel four helix bundle.	Maltose	35-42	Sec9p	Saccharomyces cerevisiae S288C	132-136
9925567-11	1999	Sequences corresponding to the AGT1 gene, which encodes a transporter of several alpha-glucosides, including maltose and maltotriose, were detected in all but one of the yeast strains.	Maltose	109-116	alpha-glucoside permease	Saccharomyces cerevisiae S288C	31-35
21644690-3	1998	We demonstrate that the redox state of immobilized cytochrome c may be modulated by the application of an electrical bias potential to the TiO(2) film and that the fluorescence yield of immobilized fluorophore-labeled maltose-binding protein may be used to monitor specifically maltose concentration.	Maltose	218-225	cytochrome c, somatic	Homo sapiens	51-63
21644690-3	1998	We demonstrate that the redox state of immobilized cytochrome c may be modulated by the application of an electrical bias potential to the TiO(2) film and that the fluorescence yield of immobilized fluorophore-labeled maltose-binding protein may be used to monitor specifically maltose concentration.	Maltose	278-285	cytochrome c, somatic	Homo sapiens	51-63
9851037-9	1998	Additionally, upstream of the maltose-degrading operon ORF1 and ORF2 are located in the opposite direction.	Maltose	30-37	hypothetical protein	Escherichia coli	55-59
9851037-9	1998	Additionally, upstream of the maltose-degrading operon ORF1 and ORF2 are located in the opposite direction.	Maltose	30-37	hypothetical protein	Escherichia coli	64-68
9700129-5	1998	This effect was abolished by the presence of 100 mM mannose (for SP-A) or maltose (for SP-D) in the culture medium, which suggested that the CRD regions of SP-A and SP-D may interact with the carbohydrate structures on the surface molecules of lymphocytes.	Maltose	74-81	surfactant protein D	Homo sapiens	87-91
9700129-5	1998	This effect was abolished by the presence of 100 mM mannose (for SP-A) or maltose (for SP-D) in the culture medium, which suggested that the CRD regions of SP-A and SP-D may interact with the carbohydrate structures on the surface molecules of lymphocytes.	Maltose	74-81	surfactant protein A1	Homo sapiens	156-160
9700129-5	1998	This effect was abolished by the presence of 100 mM mannose (for SP-A) or maltose (for SP-D) in the culture medium, which suggested that the CRD regions of SP-A and SP-D may interact with the carbohydrate structures on the surface molecules of lymphocytes.	Maltose	74-81	surfactant protein D	Homo sapiens	165-169