PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
1500176-4	1992	To evaluate the role of the FruA protein in exopolysaccharide metabolism and to assess the contribution of this enzyme to the pathogenic potential of S. mutans, a fructanase-deficient strain of S. mutans was constructed.	exopolysaccharide	44-61	fructan beta-fructosidase	Streptococcus mutans UA159	28-32
33973800-10	2021	The deletion mutants of ClpP and its subunits in ZJ173 abated pathogenicity, biofilm production, swimming ability, exopolysaccharide production, and growth in low-nutrient environments.	exopolysaccharide	115-132	clpP	Oryza sativa	24-28
34464807-5	2022	Correspondingly, the higher abundance of functional genes related to exopolysaccharide secretion (Glucokinase and UDP-glucose 4-epimerase) trigger by GP6, GP10 and GP16 was found in R2.	exopolysaccharide	69-86	glucokinase	Homo sapiens	98-109
34464807-5	2022	Correspondingly, the higher abundance of functional genes related to exopolysaccharide secretion (Glucokinase and UDP-glucose 4-epimerase) trigger by GP6, GP10 and GP16 was found in R2.	exopolysaccharide	69-86	UDP-galactose-4-epimerase	Homo sapiens	114-137
34464807-5	2022	Correspondingly, the higher abundance of functional genes related to exopolysaccharide secretion (Glucokinase and UDP-glucose 4-epimerase) trigger by GP6, GP10 and GP16 was found in R2.	exopolysaccharide	69-86	glycoprotein VI platelet	Homo sapiens	150-153
34216658-0	2021	Bacillus amyloliquefaciens exopolysaccharide preparation induces glucagon-like peptide 1 secretion through the activation of bitter taste receptors.	exopolysaccharide	27-44	glucagon	Homo sapiens	65-88
34558071-0	2022	Long-term Drench of Exopolysaccharide from Leuconostoc pseudomesenteroides XG5 Protect against Type 1 Diabetes of NOD Mice via Stimulating GLP-1 Secretion.	exopolysaccharide	20-37	glucagon	Mus musculus	139-144
34403670-0	2021	Modification and enhanced anti-inflammatory activity by Bifidobacterial fermentation of an exopolysaccharide from a medicinal fungus Cs-HK1.	exopolysaccharide	91-108	hexokinase 1	Homo sapiens	136-139
34403670-1	2021	The exopolysaccharide (EPS) from the mycelial fermentation of a medicinal fungus Cordyceps sinensis Cs-HK1 had shown significant anti-inflammatory activity previously, and EPS-LM was a highly active fraction with a relatively low molecular weight (MW) isolated from the Cs-HK1 EPS.	exopolysaccharide	4-21	hexokinase 1	Homo sapiens	103-106
34216658-1	2021	The exopolysaccharide preparation of Bacillus amyloliquefaciens amy-1 (EPS) regulates glycemic levels and promotes glucagon-like peptide 1 (GLP-1) secretion in vivo and in vitro.	exopolysaccharide	4-21	glucagon	Homo sapiens	115-138
34216658-1	2021	The exopolysaccharide preparation of Bacillus amyloliquefaciens amy-1 (EPS) regulates glycemic levels and promotes glucagon-like peptide 1 (GLP-1) secretion in vivo and in vitro.	exopolysaccharide	4-21	glucagon	Homo sapiens	140-145
7193204-2	1981	Lectin-binding activity resided in two forms of exopolysaccharide produced during growth: an apparently very high-molecular-weight capsular form and a lower-molecular-weight diffusible form.	exopolysaccharide	48-65	LOW QUALITY PROTEIN: lectin	Glycine max	0-6
35588039-0	2022	Athelia rolfsii Exopolysaccharide Protection Against Kidney Injury in Lead-Exposed Mice via Nrf2 Signaling Pathway.	exopolysaccharide	16-33	nuclear factor, erythroid derived 2, like 2	Mus musculus	92-96
35040955-0	2022	An exopolysaccharide from Bacillus subtilis alleviates airway inflammatory responses via the NF-kappaB and STAT6 pathways in asthmatic mice.	exopolysaccharide	3-20	nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105	Mus musculus	93-102
35040955-0	2022	An exopolysaccharide from Bacillus subtilis alleviates airway inflammatory responses via the NF-kappaB and STAT6 pathways in asthmatic mice.	exopolysaccharide	3-20	signal transducer and activator of transcription 6	Mus musculus	107-112
35278511-0	2022	Supramolecular structure features and immunomodulatory effects of exopolysaccharide from Paecilomyces cicadae TJJ1213 in RAW264.7 cells through NF-kappaB/MAPK signaling pathways.	exopolysaccharide	66-83	nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105	Mus musculus	144-153
33830560-6	2021	The anti-adipogenic mechanism of exopolysaccharide (EPS) isolated from L-14 extract was also analysed using Toll-like receptor 2 (TLR2) inhibitor C29.	exopolysaccharide	33-50	toll-like receptor 2	Mus musculus	130-134
33622715-6	2021	We have previously shown that coating AmB-LLs with the extracellular oligomannan-binding domain of the C-type lectin receptor Dectin-2 (DEC2-AmB-LLs) effectively targets DEC2-AmB-LLs to cell walls, exopolysaccharide matrices, and biofilms of fungal pathogens in vitro In vitro, DEC2-AmB-LLs reduce the effective dose of AmB for 95% inhibition and killing of A. fumigatus 10-fold compared to that of untargeted AmB-LLs.	exopolysaccharide	198-215	C-type lectin domain family 4, member n	Mus musculus	126-134
33278971-2	2021	Here, we aimed to evaluate the structure and bioactivity of PLN-1, an exopolysaccharide derived from the P. liquidambari NJUSTb1 strain.	exopolysaccharide	70-87	phospholamban	Mus musculus	60-63
33291425-0	2020	Exopolysaccharide Isolated from Lactobacillus plantarum L-14 Has Anti-Inflammatory Effects via the Toll-Like Receptor 4 Pathway in LPS-Induced RAW 264.7 Cells.	exopolysaccharide	0-17	toll-like receptor 4	Mus musculus	99-119
33269184-0	2020	Utilization of mixed fruit waste for exopolysaccharide production by Bacillus species SRA4: medium formulation and its optimization.	exopolysaccharide	37-54	SR-related CTD associated factor 4	Homo sapiens	86-90
32396007-0	2020	Milk Fat Globule Membrane Protects Lactobacillus rhamnosus GG from Bile Stress by Regulating Exopolysaccharide Production and Biofilm Formation.	exopolysaccharide	93-110	milk fat globule EGF and factor V/VIII domain containing	Homo sapiens	0-25
32747271-0	2020	A high-molecular weight exopolysaccharide from the Cs-HK1 fungus: Ultrasonic degradation, characterization and in vitro fecal fermentation.	exopolysaccharide	24-41	hexokinase 1	Homo sapiens	54-57
32747271-1	2020	This work was to examine the impact of power ultrasound (US) on the molecular properties of a high-molecular weight (MW) exopolysaccharide (EPS) from the Cs-HK1 medicinal fungus and the utilization, and prebiotic function of the US-treated EPS fractions in human fecal microflora in vitro.	exopolysaccharide	121-138	hexokinase 1	Homo sapiens	157-160
31201723-2	2019	A distinctly new exopolysaccharide (EPS), designated SHP-2 was obtained from S. sanghuang P0988 broth, and its structure and anti-aging prosperity were characterized.	exopolysaccharide	17-34	protein tyrosine phosphatase, non-receptor type 11	Mus musculus	53-58
30736731-9	2019	Moreover, the exopolysaccharide elicited a dose-dependent increase in nitric oxide and interleukin-10 production from RAW264.7 macrophages, concurrent with increased tumour necrosis factor-alpha secretion at all doses.	exopolysaccharide	14-31	interleukin 10	Mus musculus	87-101
31070248-3	2019	Out of forty-five, three isolates viz; ARP3, ARRP3, and ADT5 also revealed plant growth-promoting properties, including phosphate solubilization and production of siderophores, indoleacetic acid, ammonia, and exopolysaccharide.	exopolysaccharide	209-226	actin related protein 3	Homo sapiens	39-43
31028812-2	2019	This study was to evaluate the protective effects of a high-molecular weight (MW) exopolysaccharide (EPS) from a medicinal fungus Cs-HK1 on three different bifidobacteria.	exopolysaccharide	82-99	hexokinase 1	Homo sapiens	133-136
30669426-0	2019	Microcarriers Based on Glycosaminoglycan-Like Marine Exopolysaccharide for TGF-beta1 Long-Term Protection.	exopolysaccharide	53-70	transforming growth factor beta 1	Homo sapiens	75-84
30669426-6	2019	In this context, the aim of the present study was to develop microcarriers by encapsulating Transforming Growth Factor-beta1 (TGF-beta1) into microparticles based on marine exopolysaccharide (EPS), namely GY785 EPS, for further applications in cartilage engineering.	exopolysaccharide	173-190	transforming growth factor beta 1	Homo sapiens	92-124
30669426-6	2019	In this context, the aim of the present study was to develop microcarriers by encapsulating Transforming Growth Factor-beta1 (TGF-beta1) into microparticles based on marine exopolysaccharide (EPS), namely GY785 EPS, for further applications in cartilage engineering.	exopolysaccharide	173-190	transforming growth factor beta 1	Homo sapiens	126-135
28580546-11	2017	It was also found that the TC-MGF bioanode with the stable biofilm presented the nature of exopolysaccharide (EPS) structure, which is suitable for the biodegradation of the azo dye.	exopolysaccharide	91-108	signal transducer and activator of transcription 5A	Homo sapiens	30-33
30155554-4	2018	The exopolysaccharide promoted the phagocytosis of bacterial cells, activated metabolic processes in human and animal leukocytes, and moderately affected the production of TNF-alpha and IL-1beta.	exopolysaccharide	4-21	tumor necrosis factor	Homo sapiens	172-181
30155554-4	2018	The exopolysaccharide promoted the phagocytosis of bacterial cells, activated metabolic processes in human and animal leukocytes, and moderately affected the production of TNF-alpha and IL-1beta.	exopolysaccharide	4-21	interleukin 1 beta	Homo sapiens	186-194
29703735-5	2018	Further studies demonstrated that Cra directly binds to the promoters of the eps operon, ydiV, and yedQ and activates their expression, thus inhibiting motility and promoting exopolysaccharide (EPS) production and biofilm formation.	exopolysaccharide	175-192	myotubularin related protein 11	Homo sapiens	34-37
29261011-7	2018	We show that they exert nonredundant functions and demonstrate that CsrA3 and, to a lesser extent, CsrA2 but not CsrA1 alter the expression of genes involved in a variety of pathways and systems important for motility, exopolysaccharide synthesis, growth, and virulence.	exopolysaccharide	219-236	carbon storage regulator CsrA	Pseudomonas syringae pv. tomato str. DC3000	68-73
29261011-7	2018	We show that they exert nonredundant functions and demonstrate that CsrA3 and, to a lesser extent, CsrA2 but not CsrA1 alter the expression of genes involved in a variety of pathways and systems important for motility, exopolysaccharide synthesis, growth, and virulence.	exopolysaccharide	219-236	carbon storage regulator CsrA	Pseudomonas syringae pv. tomato str. DC3000	99-104
28733286-2	2017	Despite LTTRs being global regulators of pathogenicity in several types of bacteria, few have been characterized in Burkholderia Here, we show that gene ldhR of B. multivorans encoding an LTTR is cotranscribed with ldhA encoding a d-lactate dehydrogenase and evaluate their implication in virulence traits such as exopolysaccharide (EPS) synthesis and biofilm formation.	exopolysaccharide	314-331	lactate dehydrogenase A	Homo sapiens	215-219
30036626-0	2018	Protection of Bifidobacterial cells against antibiotics by a high molecular weight exopolysaccharide of a medicinal fungus Cs-HK1 through physical interactions.	exopolysaccharide	83-100	hexokinase 1	Homo sapiens	126-129
30036626-1	2018	This study was to assess the protective effect of exopolysaccharide (EPS) produced by a medicinal fungus Cordyceps sinensis Cs-HK1 on Bifidobacteria against antibiotic inhibition.	exopolysaccharide	50-67	hexokinase 1	Homo sapiens	127-130
29763807-8	2018	The novel engineered peptides encompass both the LPS-binding and aggregation-prone regions of parental ECP, providing the appropriate structural features for peptide attachment to the bacterial exopolysaccharide layer and bacterial cell membrane destabilization, thereby promoting biofilm removal at micro molar concentrations.	exopolysaccharide	194-211	ribonuclease A family member 3	Homo sapiens	103-106
28495632-0	2017	Evaluation of dermal wound healing activity and in vitro antibacterial and antioxidant activities of a new exopolysaccharide produced by Lactobacillus sp.Ca6.	exopolysaccharide	107-124	carbonic anhydrase 6	Rattus norvegicus	154-157
28605194-1	2017	Bacterial biofilms form when bacteria adhere to a surface and produce an exopolysaccharide matrix ( Costerton Science 1999 , 284 , 1318 ; Davies Science 1998 , 280 , 295 ; Flemming Nat.	exopolysaccharide	73-90	bromodomain containing 2	Homo sapiens	181-184
30108811-1	2017	Carboxymethylated and sulfated polysaccharides (CLEP and SLEP) were prepared from an exopolysaccharide previously obtained from Lachnum YM240 (LEP) by chemical modifications.	exopolysaccharide	85-102	leptin	Mus musculus	49-52
27486751-0	2016	Exopolysaccharide Production by Sinorhizobium fredii HH103 Is Repressed by Genistein in a NodD1-Dependent Manner.	exopolysaccharide	0-17	transcriptional regulator NodD1	Sinorhizobium fredii NGR234	90-95
27503246-2	2017	In Pseudomonas aeruginosa, FleQ functions as a c-di-GMP-dependent transcriptional regulator of expression of flagellar genes and the exopolysaccharide (EPS) Pel, a component of the biofilm extracellular matrix.	exopolysaccharide	133-150	sigma-54-dependent Fis family transcriptional regulator	Pseudomonas putida KT2440	27-31
27357535-0	2016	Evaluation of the angiogenic potency of a novel exopolysaccharide produced by the MK1 bacterial strain.	exopolysaccharide	48-65	potassium voltage-gated channel subfamily A member 1	Homo sapiens	82-85
27357535-2	2016	Here, we evaluated the angiogenic properties of an exopolysaccharide (EPS) secreted by MK1 (MK1-EPS), a novel bacterial strain isolated from Neungee mushrooms.	exopolysaccharide	51-68	potassium voltage-gated channel subfamily A member 1	Homo sapiens	87-90
27357535-2	2016	Here, we evaluated the angiogenic properties of an exopolysaccharide (EPS) secreted by MK1 (MK1-EPS), a novel bacterial strain isolated from Neungee mushrooms.	exopolysaccharide	51-68	potassium voltage-gated channel subfamily A member 1	Homo sapiens	92-95
27486751-3	2016	In this work we show that the production of exopolysaccharide by Sinorhizobium fredii HH103, but not by other S. fredii strains such as USDA257 or NGR234, is repressed by nod gene inducing flavonoids such as genistein and that this repression is dependent on the presence of a functional NodD1 protein.	exopolysaccharide	44-61	transcriptional regulator NodD1	Sinorhizobium fredii NGR234	288-293
26733973-11	2015	Thus, the modulation of structural characteristics of exopolysaccharide by vicX provides new insights into the interaction between the exopolysaccharide structure, gene functions, and cariogenicity.	exopolysaccharide	54-71	MBL fold metallo-hydrolase	Streptococcus mutans UA159	75-79
25938977-2	2016	Ebosin, a novel exopolysaccharide (EPS), exhibits anti-inflammatory activity in rat collagen-induced arthritis by suppressing the production of tumor necrosis factor-alpha, interleukin-6 and interleukin-1beta.	exopolysaccharide	16-33	tumor necrosis factor	Rattus norvegicus	144-171
25938977-2	2016	Ebosin, a novel exopolysaccharide (EPS), exhibits anti-inflammatory activity in rat collagen-induced arthritis by suppressing the production of tumor necrosis factor-alpha, interleukin-6 and interleukin-1beta.	exopolysaccharide	16-33	interleukin 6	Rattus norvegicus	173-186
25938977-2	2016	Ebosin, a novel exopolysaccharide (EPS), exhibits anti-inflammatory activity in rat collagen-induced arthritis by suppressing the production of tumor necrosis factor-alpha, interleukin-6 and interleukin-1beta.	exopolysaccharide	16-33	interleukin 1 beta	Rattus norvegicus	191-208
26733973-5	2015	Here, we identified the role of vicX in the structural characteristics of the exopolysaccharide matrix and biofilm physiology.	exopolysaccharide	78-95	MBL fold metallo-hydrolase	Streptococcus mutans UA159	32-36
26733973-6	2015	The vicX mutant (SmuvicX) biofilms seemingly exhibited "desertification" with architecturally impaired exopolysaccharide-enmeshed cell clusters, compared with the UA159 strain (S. mutans wild type strain).	exopolysaccharide	103-120	MBL fold metallo-hydrolase	Streptococcus mutans UA159	4-8
26884212-4	2016	Deletion of ahpC led to a severe growth defect in rich media that was not observed in minimal media and promoted early biofilm formation through increased production of exopolysaccharide (EPS) and EPS gene expression.	exopolysaccharide	169-186	alkyl hydroperoxide reductase subunit F	Acinetobacter oleivorans DR1	12-16
26733973-11	2015	Thus, the modulation of structural characteristics of exopolysaccharide by vicX provides new insights into the interaction between the exopolysaccharide structure, gene functions, and cariogenicity.	exopolysaccharide	135-152	MBL fold metallo-hydrolase	Streptococcus mutans UA159	75-79
26733973-12	2015	Our results suggest that vicX gene modulates the structural characteristics of exopolysaccharide associated with cariogenicity, which may be explored as a potential target that contributes to dental caries management.	exopolysaccharide	79-96	MBL fold metallo-hydrolase	Streptococcus mutans UA159	25-29
25498701-1	2015	An exopolysaccharide, obtained previously LEP-2b from Lachnum YM405, was phosphated and sulfated successfully.	exopolysaccharide	3-20	late cornified envelope 1B	Homo sapiens	42-47
25659678-2	2015	The aim of this study was to investigate the anticancer activity of exopolysaccharide (PEP) of Antarctic bacterium Pseudoaltermonas sp.	exopolysaccharide	68-85	progestagen associated endometrial protein	Homo sapiens	87-90
25320181-0	2014	Exopolysaccharide-producing probiotic Lactobacilli reduce serum cholesterol and modify enteric microbiota in ApoE-deficient mice.	exopolysaccharide	0-17	apolipoprotein E	Mus musculus	109-113
26852488-1	2015	By flow cytometry it was demonstrated that lipopolysaccharide and exopolysaccharide of marine proteobacteria Pseudoalteromonas nigrifaciens alter the expression of adhesion molecules on human neutrophils and monocytes, reducing the expression level of molecules CD62L and increasing the expression of CD11b, CD11c and CD54.	exopolysaccharide	66-83	selectin L	Homo sapiens	262-267
26852488-1	2015	By flow cytometry it was demonstrated that lipopolysaccharide and exopolysaccharide of marine proteobacteria Pseudoalteromonas nigrifaciens alter the expression of adhesion molecules on human neutrophils and monocytes, reducing the expression level of molecules CD62L and increasing the expression of CD11b, CD11c and CD54.	exopolysaccharide	66-83	integrin subunit alpha M	Homo sapiens	301-306
26852488-1	2015	By flow cytometry it was demonstrated that lipopolysaccharide and exopolysaccharide of marine proteobacteria Pseudoalteromonas nigrifaciens alter the expression of adhesion molecules on human neutrophils and monocytes, reducing the expression level of molecules CD62L and increasing the expression of CD11b, CD11c and CD54.	exopolysaccharide	66-83	integrin subunit alpha X	Homo sapiens	308-313
26852488-1	2015	By flow cytometry it was demonstrated that lipopolysaccharide and exopolysaccharide of marine proteobacteria Pseudoalteromonas nigrifaciens alter the expression of adhesion molecules on human neutrophils and monocytes, reducing the expression level of molecules CD62L and increasing the expression of CD11b, CD11c and CD54.	exopolysaccharide	66-83	intercellular adhesion molecule 1	Homo sapiens	318-322
25653152-1	2015	A new PCR-based method to detect putative exopolysaccharide (EPS) producers from the genus Bifidobacterium was developed based on the detection of two priming glycosyltransferase genes: rfbP (undecaprenyl-phosphate sugar phospho-transferase) and cpsD (galactosyl-transferase).	exopolysaccharide	42-59	cathepsin D	Homo sapiens	246-250
25320181-2	2014	OBJECTIVES: The aim of this study was to assess the impact of dietary administration of exopolysaccharide-producing probiotic Lactobacillus cultures on lipid metabolism and gut microbiota in apolipoprotein E (apoE)-deficient mice.	exopolysaccharide	88-105	apolipoprotein E	Mus musculus	209-213
24343648-6	2014	Intradermal administration of an exoproteome extract of an exopolysaccharide-dependent biofilm induced a humoral immune response and elicited the production of interleukin 10 (IL-10) and IL-17 in mice.	exopolysaccharide	59-76	interleukin 10	Mus musculus	160-174
24314091-11	2014	SIGNIFICANCE AND IMPACT OF THE STUDY: This report demonstrates a food-applicable Leuconostoc mesenteroides strain secreting exopolysaccharide that shows high IgA-inducing ability.	exopolysaccharide	124-141	immunoglobulin heavy constant alpha	Mus musculus	158-161
24354946-5	2014	SIGNIFICANCE AND IMPACT OF THE STUDY: The exopolysaccharide produced by B. licheniformis strain T14, stimulator of Th1 cell-mediated immunity, could be used as therapy in immunocompromised host.	exopolysaccharide	42-59	negative elongation factor complex member C/D	Homo sapiens	115-118
25101646-5	2014	The last gene of the cluster encodes the fourth listerial GGDEF domain protein, PssE, that functions as an I-site c-di-GMP receptor essential for exopolysaccharide synthesis.	exopolysaccharide	146-163	5'-nucleotidase, cytosolic II	Mus musculus	119-122
25101646-6	2014	The c-di-GMP-inducible exopolysaccharide causes cell aggregation in minimal medium and impairs bacterial migration in semi-solid agar, however, it does not promote biofilm formation on abiotic surfaces.	exopolysaccharide	23-40	5'-nucleotidase, cytosolic II	Mus musculus	9-12
25101646-8	2014	The exopolysaccharide and another, as yet unknown c-di-GMP-dependent target, drastically decrease listerial invasiveness in enterocytes in vitro, and lower pathogen load in the liver and gallbladder of mice infected via an oral route, which suggests that elevated c-di-GMP levels play an overall negative role in listerial virulence.	exopolysaccharide	4-21	5'-nucleotidase, cytosolic II	Mus musculus	55-58
25101646-8	2014	The exopolysaccharide and another, as yet unknown c-di-GMP-dependent target, drastically decrease listerial invasiveness in enterocytes in vitro, and lower pathogen load in the liver and gallbladder of mice infected via an oral route, which suggests that elevated c-di-GMP levels play an overall negative role in listerial virulence.	exopolysaccharide	4-21	5'-nucleotidase, cytosolic II	Mus musculus	269-272
24343648-6	2014	Intradermal administration of an exoproteome extract of an exopolysaccharide-dependent biofilm induced a humoral immune response and elicited the production of interleukin 10 (IL-10) and IL-17 in mice.	exopolysaccharide	59-76	interleukin 10	Mus musculus	176-181
24343648-6	2014	Intradermal administration of an exoproteome extract of an exopolysaccharide-dependent biofilm induced a humoral immune response and elicited the production of interleukin 10 (IL-10) and IL-17 in mice.	exopolysaccharide	59-76	interleukin 17A	Mus musculus	187-192
24123746-0	2014	Genomic overview and biological functions of exopolysaccharide biosynthesis in Bifidobacterium spp.	exopolysaccharide	45-62	histocompatibility minor 13	Homo sapiens	95-98
23274679-1	2013	A neutral exopolysaccharide (EPS), designated LPC-1, was isolated from the culture of Lactobacillus plantarum C88 and purified by ion-exchange and gel-permeation chromatography.	exopolysaccharide	10-27	annexin A1	Homo sapiens	46-51
22966120-6	2012	Because the alginate exopolysaccharide is surface-exposed, levels of SP-A may be crucial to modulate the interaction of P. aeruginosa with AEC.	exopolysaccharide	21-38	surfactant protein A1	Homo sapiens	69-73
22127129-0	2011	Exopolysaccharide-overproducing Lactobacillus paracasei KB28 induces cytokines in mouse peritoneal macrophages via modulation of NF-kappabeta and MAPKs.	exopolysaccharide	0-17	nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105	Mus musculus	129-141
21166709-0	2011	Ssg, a putative glycosyltransferase, functions in lipo- and exopolysaccharide biosynthesis and cell surface-related properties in Pseudomonas alkylphenolia.	exopolysaccharide	60-77	PSAKL28_RS12075	Pseudomonas alkylphenolica	16-35
21248858-3	2011	Chemical analysis showed that this exopolysaccharide was a levan (beta-2, 6-linked fructan).	exopolysaccharide	35-52	hemoglobin, beta adult minor chain	Mus musculus	66-72
19929968-2	2010	In Sinorhizobium meliloti, the regulatory protein MucR controls exopolysaccharide production.	exopolysaccharide	64-81	putative transcription regulator protein	Sinorhizobium meliloti	50-54
21221951-6	2010	An exopolysaccharide purified from the acidophilic strain was added to cultured U937 cells, resulting in significantly increased transcription levels of p53 and p21 genes.	exopolysaccharide	3-20	tumor protein p53	Homo sapiens	153-156
21221951-6	2010	An exopolysaccharide purified from the acidophilic strain was added to cultured U937 cells, resulting in significantly increased transcription levels of p53 and p21 genes.	exopolysaccharide	3-20	H3 histone pseudogene 16	Homo sapiens	161-164
14987774-0	2004	Disruption of dTDP-rhamnose biosynthesis modifies lipopolysaccharide core, exopolysaccharide production, and root colonization in Azospirillum brasilense.	exopolysaccharide	75-92	TAR DNA-binding protein-43 homolog	Drosophila melanogaster	14-18
19182778-5	2009	In the squid symbiont V. fischeri ES114, RscS controls light-organ colonization by inducing the Syp exopolysaccharide, a mediator of biofilm formation during initial infection.	exopolysaccharide	100-117	activator of syp locus genes	Vibrio fischeri ES114	41-45
18842098-0	2008	Sinorhizobium meliloti regulator MucR couples exopolysaccharide synthesis and motility.	exopolysaccharide	46-63	putative transcription regulator protein	Sinorhizobium meliloti	33-37
17531137-6	2007	In this paper, we have established an automatic quantitative analysis to evaluate a modulator effect of a sulphated exopolysaccharide on FGF-2-induced in vitro angiogenesis, according to different parameters.	exopolysaccharide	116-133	fibroblast growth factor 2	Homo sapiens	137-142
16917538-7	2006	The presence of hexadecane negatively affected these activities and lowered the amounts of exopolysaccharides in CNP and P biofilms in fall 1999 but increased the biofilm activities and exopolysaccharide amounts in CNP biofilm in fall 2001.	exopolysaccharide	91-108	2',3'-cyclic nucleotide 3' phosphodiesterase	Homo sapiens	113-116
16301659-0	2005	The exopolysaccharide alginate protects Pseudomonas aeruginosa biofilm bacteria from IFN-gamma-mediated macrophage killing.	exopolysaccharide	4-21	interferon gamma	Homo sapiens	85-94
16325517-0	2005	Effects of exopolysaccharide fraction (EPSF) from a cultivated Cordyceps sinensis fungus on c-Myc, c-Fos, and VEGF expression in B16 melanoma-bearing mice.	exopolysaccharide	11-28	vascular endothelial growth factor A	Mus musculus	110-114
19388274-1	2009	OBJECTIVE: To study the inhibition of human gastric cancer cell line BGC-823 by exopolysaccharide (B. EPS) extracted from Bifidobacterium bifidum and the effect on the activity of telomerase rate-limiting factor human telomerase reverse transcriptase (hTERT).	exopolysaccharide	80-97	telomerase reverse transcriptase	Homo sapiens	252-257
16598021-6	2006	LacZ and PhoA translational fusions with PslD indicated that PslD is a secreted protein required for biofilm formation, presumably via its role in exopolysaccharide export.	exopolysaccharide	147-164	biofilm formation protein PslD	Pseudomonas aeruginosa PAO1	61-65
15710353-0	2005	Effect of an oversulfated exopolysaccharide on angiogenesis induced by fibroblast growth factor-2 or vascular endothelial growth factor in vitro.	exopolysaccharide	26-43	fibroblast growth factor 2	Homo sapiens	71-97
15710353-0	2005	Effect of an oversulfated exopolysaccharide on angiogenesis induced by fibroblast growth factor-2 or vascular endothelial growth factor in vitro.	exopolysaccharide	26-43	vascular endothelial growth factor A	Homo sapiens	101-135
10491103-0	1999	Structure determination of an exopolysaccharide from an alkaliphilic bacterium closely related to Bacillus spp.	exopolysaccharide	30-47	histocompatibility minor 13	Homo sapiens	107-110
16349537-1	1998	Hyphomonas strain MHS-3, a member of a genus of primary colonizers of surfaces immersed in marine water, synthesizes two structures that mediate adhesion to solid substrata, namely, capsular exopolysaccharide and fimbriae.	exopolysaccharide	191-208	MHS3	Homo sapiens	18-23