PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
2827377-2	1988	Identification of the dissociation products of the isolated oligomer and comparison of the number of N-linked glycans in native and denatured NS1 is consistent with the idea that the high-molecular-weight form of NS1 is a homodimer.	n-linked glycans	101-117	influenza virus NS1A binding protein	Homo sapiens	213-216
3143729-9	1988	The mature form of MGA (MGAm) bears in addition to N-linked glycans also O-glycosidically linked oligosaccharides.	n-linked glycans	51-67	maltase-glucoamylase	Homo sapiens	19-22
3143729-9	1988	The mature form of MGA (MGAm) bears in addition to N-linked glycans also O-glycosidically linked oligosaccharides.	n-linked glycans	51-67	maltase-glucoamylase	Homo sapiens	24-28
3346246-15	1988	Our data on the biosynthesis show that the early MAM-6 precursors contain N-linked glycans, suggesting the presence of N-linked glycans on the mature MAM-6 molecule.	n-linked glycans	74-90	mucin 1, cell surface associated	Homo sapiens	49-54
3346246-15	1988	Our data on the biosynthesis show that the early MAM-6 precursors contain N-linked glycans, suggesting the presence of N-linked glycans on the mature MAM-6 molecule.	n-linked glycans	74-90	mucin 1, cell surface associated	Homo sapiens	150-155
3346246-15	1988	Our data on the biosynthesis show that the early MAM-6 precursors contain N-linked glycans, suggesting the presence of N-linked glycans on the mature MAM-6 molecule.	n-linked glycans	119-135	mucin 1, cell surface associated	Homo sapiens	49-54
3346246-15	1988	Our data on the biosynthesis show that the early MAM-6 precursors contain N-linked glycans, suggesting the presence of N-linked glycans on the mature MAM-6 molecule.	n-linked glycans	119-135	mucin 1, cell surface associated	Homo sapiens	150-155
2523254-1	1989	Our earlier studies revealed that N-acetylglucosaminyltransferase III (GnTase III), which catalyzes the insertion of a bisecting N-acetylglucosamine (bi-Gn) in the complex-type N-linked glycans of cellular glycoproteins, is present in hepatic nodules promoted by the orotic acid model.	n-linked glycans	177-193	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Rattus norvegicus	34-69
2538547-0	1989	Role of N-linked glycans in the interaction between the envelope glycoprotein of human immunodeficiency virus and its CD4 cellular receptor.	n-linked glycans	8-24	CD4 molecule	Homo sapiens	118-121
3084653-9	1986	This considerable charge heterogeneity is consistent with the possibility that other posttranslational modifications to the mouse IL 2 receptor occur besides addition of complex N-linked glycans.	n-linked glycans	178-194	interleukin 2	Mus musculus	130-134
3301835-8	1987	The N-linked glycans on human and mouse glycoprotein IIa are all of the complex type.	n-linked glycans	4-20	ATPase, class II, type 9A	Mus musculus	53-56
6098655-10	1984	Neither Mr = 33,000 and 24,000 fragment appear to be substrates for endo-beta-N-acetylglucosaminidase F. These data allow us to conclude that the hepatic glucagon receptor in the membrane is a dimer of approximately 60,000 dalton hormone binding subunit which is a glycoprotein containing at least four N-linked glycans accounting for 18,000 daltons of its mass.	n-linked glycans	303-319	glucagon receptor	Homo sapiens	154-171
2870429-6	1986	Digestion of Thy-1 with endo-beta-galactosidase suggested that the complex type N-linked glycans in thymocytes, but not in lymph node T-cells, contained increased levels of polylactosamine.	n-linked glycans	80-96	thymus cell antigen 1, theta	Mus musculus	13-18
2870429-6	1986	Digestion of Thy-1 with endo-beta-galactosidase suggested that the complex type N-linked glycans in thymocytes, but not in lymph node T-cells, contained increased levels of polylactosamine.	n-linked glycans	80-96	galactosidase, beta 1	Mus musculus	29-47
34012659-11	2021	We also observed the increased ER degradation-enhancing alpha-mannosidase-like protein 3 (EDEM3), which is trimming of N-linked glycans by sequential removal of mannose residues, might result in more non-N-glycosylated form of BST-2.	n-linked glycans	119-135	ER degradation enhancing alpha-mannosidase like protein 3	Homo sapiens	31-88
34013301-2	2021	Cross-reactive antibodies specifically recognized the sialic acid moiety on N-linked glycans of the Spike protein and do not neutralize in vitro SARS-CoV-2.	n-linked glycans	76-92	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	100-105
34012659-11	2021	We also observed the increased ER degradation-enhancing alpha-mannosidase-like protein 3 (EDEM3), which is trimming of N-linked glycans by sequential removal of mannose residues, might result in more non-N-glycosylated form of BST-2.	n-linked glycans	119-135	ER degradation enhancing alpha-mannosidase like protein 3	Homo sapiens	90-95
34012659-11	2021	We also observed the increased ER degradation-enhancing alpha-mannosidase-like protein 3 (EDEM3), which is trimming of N-linked glycans by sequential removal of mannose residues, might result in more non-N-glycosylated form of BST-2.	n-linked glycans	119-135	bone marrow stromal cell antigen 2	Homo sapiens	227-232
33607086-12	2021	After removing N-linked glycans on ACE2, its mechanical binding strength with CoV-2 RBD decreases to a similar level of the CoV-1 RBD-ACE2 interaction.	n-linked glycans	15-31	angiotensin converting enzyme 2	Homo sapiens	35-39
33669676-4	2021	While the envelope (Env) protein is the only viral protein present on the surface of virions, it exists in a complex trimeric conformation and is decorated with an array of variable N-linked glycans, making it an important but difficult target for vaccine design.	n-linked glycans	182-198	endogenous retrovirus group K member 20	Homo sapiens	20-23
33758835-2	2021	The abundance of N-linked glycans across the SARS-CoV-2 spike protein is a potential source of heterogeneity between the many different vaccine candidates under investigation.	n-linked glycans	17-33	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	56-61
33134321-6	2020	We used structural modeling to test this idea, and show that N-linked glycans appear to restrict torsinA"s ability to form closed homohexameric ring assemblies, and instead promote an open hexameric conformation that allows torsinA interaction with key cofactors required for ATP hydrolysis.	n-linked glycans	61-77	torsin family 1 member A	Homo sapiens	97-104
33301684-4	2021	Herein, we introduce a radically simplified sample preparation workflow, with direct ESI-MS analysis, enabling the quantification of N-linked glycans that originate from uromodulin.	n-linked glycans	133-149	uromodulin	Homo sapiens	170-180
32915505-0	2020	Structural characterization of the N-linked glycans in the receptor binding domain of the SARS-CoV-2 spike protein and their interactions with human lectins using NMR spectroscopy.	n-linked glycans	35-51	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	101-106
33292056-0	2022	Sensing the interactions between carbohydrate-binding agents and N-linked glycans of SARS-CoV-2 spike glycoprotein using molecular docking and simulation studies.	n-linked glycans	65-81	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	96-101
33292056-2	2022	The homotrimeric transmembrane spike (S) glycoprotein of coronaviruses which facilitates virus entry into the host cells is covered with N-linked glycans having oligomannose and complex sugars.	n-linked glycans	137-153	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	31-36
33093196-1	2020	The dense array of N-linked glycans on the HIV-1 envelope glycoprotein (Env), known as the "glycan shield," is a key determinant of immunogenicity, yet intrinsic heterogeneity confounds typical structure-function analysis.	n-linked glycans	19-35	endogenous retrovirus group K member 20	Homo sapiens	49-70
33093196-1	2020	The dense array of N-linked glycans on the HIV-1 envelope glycoprotein (Env), known as the "glycan shield," is a key determinant of immunogenicity, yet intrinsic heterogeneity confounds typical structure-function analysis.	n-linked glycans	19-35	endogenous retrovirus group K member 20	Homo sapiens	72-75
33134321-6	2020	We used structural modeling to test this idea, and show that N-linked glycans appear to restrict torsinA"s ability to form closed homohexameric ring assemblies, and instead promote an open hexameric conformation that allows torsinA interaction with key cofactors required for ATP hydrolysis.	n-linked glycans	61-77	torsin family 1 member A	Homo sapiens	224-231
32675574-1	2020	PURPOSE OF REVIEW: The surface of the HIV-1 Env glycoprotein, the target of neutralizing antibodies, is extensively covered by N-linked glycans that create a glycan shield.	n-linked glycans	127-143	endogenous retrovirus group K member 20	Homo sapiens	44-47
32699088-2	2020	For enveloped viruses such as the influenza A virus (IAV), the addition of large N-linked glycans can also prevent access to epitopes on the surface antigens hemagglutinin (HA or H) and neuraminidase (NA or N).	n-linked glycans	81-97	neuraminidase 1	Homo sapiens	186-199
32356523-2	2020	It has been demonstrated that the carbohydrate-recognition domain (CRD) of ERGIC-53 (ERGIC-53CRD) interacts with N-linked glycans on cargo glycoproteins, whereas MCFD2 recognizes polypeptide segments of cargo glycoproteins.	n-linked glycans	113-129	lectin, mannose binding 1	Homo sapiens	75-83
32454127-3	2020	In prion disease, the N-linked glycans and GPI-anchor on the prion protein (PrP) impair fibril assembly.	n-linked glycans	22-38	prion protein	Mus musculus	76-79
32766576-12	2020	After the removal of N-linked glycans on ACE2, its mechanical binding strength with CoV-2 RBD decreases to a similar level of the CoV-1 RBD-ACE2 interaction.	n-linked glycans	21-37	angiotensin converting enzyme 2	Homo sapiens	41-45
32766576-12	2020	After the removal of N-linked glycans on ACE2, its mechanical binding strength with CoV-2 RBD decreases to a similar level of the CoV-1 RBD-ACE2 interaction.	n-linked glycans	21-37	angiotensin converting enzyme 2	Homo sapiens	140-144
32108991-3	2020	Furthermore, N-linked glycans within the A2-domain have been shown to protect VWF against premature LRP1-mediated clearance.	n-linked glycans	13-29	Von Willebrand factor	Mus musculus	78-81
32108991-3	2020	Furthermore, N-linked glycans within the A2-domain have been shown to protect VWF against premature LRP1-mediated clearance.	n-linked glycans	13-29	low density lipoprotein receptor-related protein 1	Mus musculus	100-104
32203567-5	2020	Genomic and structural analyses reveal that beta-catenin/CBP signaling represses fucosylation on the antennae of N-linked glycans on EGFR.	n-linked glycans	113-129	catenin beta 1	Homo sapiens	44-56
32203567-5	2020	Genomic and structural analyses reveal that beta-catenin/CBP signaling represses fucosylation on the antennae of N-linked glycans on EGFR.	n-linked glycans	113-129	CREB binding protein	Homo sapiens	57-60
32203567-5	2020	Genomic and structural analyses reveal that beta-catenin/CBP signaling represses fucosylation on the antennae of N-linked glycans on EGFR.	n-linked glycans	113-129	epidermal growth factor receptor	Homo sapiens	133-137
32356523-2	2020	It has been demonstrated that the carbohydrate-recognition domain (CRD) of ERGIC-53 (ERGIC-53CRD) interacts with N-linked glycans on cargo glycoproteins, whereas MCFD2 recognizes polypeptide segments of cargo glycoproteins.	n-linked glycans	113-129	lectin, mannose binding 1	Homo sapiens	85-96
32157792-5	2020	Mechanistically, we showed that GLT1D1 transferred N-linked glycans to PD-L1, thus promoting the immunosuppressive function of glycosylated PD-L1.	n-linked glycans	51-67	glycosyltransferase 1 domain containing 1	Mus musculus	32-38
32157792-5	2020	Mechanistically, we showed that GLT1D1 transferred N-linked glycans to PD-L1, thus promoting the immunosuppressive function of glycosylated PD-L1.	n-linked glycans	51-67	CD274 antigen	Mus musculus	71-76
32157792-5	2020	Mechanistically, we showed that GLT1D1 transferred N-linked glycans to PD-L1, thus promoting the immunosuppressive function of glycosylated PD-L1.	n-linked glycans	51-67	CD274 antigen	Mus musculus	140-145
31471298-1	2019	OBJECTIVE: Anti-citrullinated protein antibodies (ACPA) in rheumatoid arthritis (RA) patients display a unique feature defined by the abundant presence of N-linked glycans within the variable domains (V-domains).	n-linked glycans	155-171	proteinase 3	Homo sapiens	50-54
31996426-7	2020	Pretreatment of EHV1 virions with eBD2 and -3 increased the subsequent infection of rabbit kidney (RK13) cells, which was dependent on viral N-linked glycans.	n-linked glycans	141-157	ebd2 and -3	None	34-45
31636418-8	2019	In contrast, polymorphic sites and N-linked glycans are preferentially found in exposed positions on the receptor surface, not contacting transferrin, suggesting that transferrin receptor diversification is driven by a need for antigenic variation in the receptor to prolong survival in a host.	n-linked glycans	35-51	transferrin receptor	Homo sapiens	167-187
30973186-1	2019	The biological activity of the glycoprotein hormone erythropoietin (EPO) is dependent mainly on the structure of its N-linked glycans.	n-linked glycans	117-133	erythropoietin	Homo sapiens	52-66
31266804-8	2019	Deletion of the mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase (MGAT1), necessary for the generation of complex N-linked glycans, abrogated TRPC6 gain-of-function variant-mediated Ca2+ influx and extracellular signal-regulated kinase activation in HEK cells, but failed to diminish cytotoxicity in cultured podocytes.	n-linked glycans	141-157	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	93-98
31266804-8	2019	Deletion of the mannosyl (alpha-1,3-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase (MGAT1), necessary for the generation of complex N-linked glycans, abrogated TRPC6 gain-of-function variant-mediated Ca2+ influx and extracellular signal-regulated kinase activation in HEK cells, but failed to diminish cytotoxicity in cultured podocytes.	n-linked glycans	141-157	transient receptor potential cation channel subfamily C member 6	Homo sapiens	169-174
31667130-5	2019	Selective DPAGT1 inhibitors have the promising therapeutic potential for certain solid cancers that require increased branching of N-linked glycans in their growth progressions.	n-linked glycans	131-147	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Rattus norvegicus	10-16
31336133-6	2019	The aim of the present study was to compare the influence of ANITVNITV peptide fusion on the physicochemical, biological and pharmacokinetic properties of native hIFN-alpha2b (IFNwt), which contains a single O-glycosylation site, and a hyperglycosylated variant (IFN4N), that bears, in addition, 4 N-linked glycans.	n-linked glycans	298-314	interferon alpha 2	Homo sapiens	162-174
31364612-4	2019	For a standard protein ovalbumin digest, 26 N-linked glycans were identified with good repeatability, and the detection limit was as low as 0.25 ng muL-1 with the identification of 13 N-linked glycans (S/N > 10).	n-linked glycans	184-200	mitochondrial E3 ubiquitin protein ligase 1	Homo sapiens	148-153
31308178-4	2019	Here, using glycoside hydrolase and kinase assays and immunoprecipitation and MS-based analyses, we demonstrate that N-linked glycans at the Asn-247 site in VEGFR2 hinder VEGF ligand-mediated receptor activation and signaling in endothelial cells.	n-linked glycans	117-133	kinase insert domain receptor	Homo sapiens	157-163
31308178-4	2019	Here, using glycoside hydrolase and kinase assays and immunoprecipitation and MS-based analyses, we demonstrate that N-linked glycans at the Asn-247 site in VEGFR2 hinder VEGF ligand-mediated receptor activation and signaling in endothelial cells.	n-linked glycans	117-133	vascular endothelial growth factor A	Homo sapiens	157-161
30973186-1	2019	The biological activity of the glycoprotein hormone erythropoietin (EPO) is dependent mainly on the structure of its N-linked glycans.	n-linked glycans	117-133	erythropoietin	Homo sapiens	68-71
30842877-4	2019	Detailed mass spectrometric structural analysis showed an increase in disialo-biantennary N-linked glycans on IgA1 from BCa patients (p < 0.0001: non-core fucosylated; p = 0.0345: core fucosylated) and increased asialo-Thomsen-Friedenreich antigen (TF) and disialo-TF antigens in the O-linked glycan preparations from IgA1 of cancer patients compared with healthy control individuals.	n-linked glycans	90-106	immunoglobulin heavy constant alpha 1	Homo sapiens	110-114
31311973-4	2019	Using structures as a guide, we show that the N-linked glycans at the interface of GluK3 ATD and LBD likely mediate inter-domain interactions and attune receptor-gating properties.	n-linked glycans	46-62	glutamate ionotropic receptor kainate type subunit 3	Homo sapiens	83-88
31211781-0	2019	Identification of N-linked glycans as specific mediators of neuronal uptake of acetylated alpha-Synuclein.	n-linked glycans	18-34	synuclein alpha	Homo sapiens	90-105
30842877-4	2019	Detailed mass spectrometric structural analysis showed an increase in disialo-biantennary N-linked glycans on IgA1 from BCa patients (p < 0.0001: non-core fucosylated; p = 0.0345: core fucosylated) and increased asialo-Thomsen-Friedenreich antigen (TF) and disialo-TF antigens in the O-linked glycan preparations from IgA1 of cancer patients compared with healthy control individuals.	n-linked glycans	90-106	immunoglobulin heavy constant alpha 1	Homo sapiens	321-325
30476078-7	2019	Interestingly, Lewisx was mainly carried by N-linked glycans in both MC38-FUT4 and MC38-FUT9 cells, despite pronounced differences in the biosynthetic properties and the expression stability of the induced enzymes.	n-linked glycans	44-60	fucosyltransferase 4	Mus musculus	15-21
30737276-3	2019	The structures of the four N-linked glycans from the PBCV-1 MCP consist of nonasaccharides, and similar glycans are not found elsewhere in the three domains of life.	n-linked glycans	27-43	Major capsid protein	Paramecium bursaria Chlorella virus 1	60-63
30740857-13	2019	CLEC4M binding to recombinant FVIII was dependent on mannose-exposed N-linked glycans.	n-linked glycans	69-85	C-type lectin domain family 4 member M	Homo sapiens	0-6
30740857-13	2019	CLEC4M binding to recombinant FVIII was dependent on mannose-exposed N-linked glycans.	n-linked glycans	69-85	coagulation factor VIII	Homo sapiens	30-35
30476078-7	2019	Interestingly, Lewisx was mainly carried by N-linked glycans in both MC38-FUT4 and MC38-FUT9 cells, despite pronounced differences in the biosynthetic properties and the expression stability of the induced enzymes.	n-linked glycans	44-60	fucosyltransferase 9	Mus musculus	88-92
30375453-9	2018	Systems with N-linked glycans encountered higher energy barriers for full unfolding and even for unfolding up to the point of ADAMTS13 cleavage site exposure.	n-linked glycans	13-29	ADAM metallopeptidase with thrombospondin type 1 motif 13	Homo sapiens	126-134
30355496-1	2018	Densely arranged N-linked glycans shield the HIV-1 envelope (Env) trimer from antibody recognition.	n-linked glycans	17-33	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	51-59
30355496-1	2018	Densely arranged N-linked glycans shield the HIV-1 envelope (Env) trimer from antibody recognition.	n-linked glycans	17-33	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	61-64
30054538-9	2018	To test whether the microglial response is mediated by carbohydrate epitopes on PrPSc surface, the levels of sialylation of PrPSc N-linked glycans was altered by treatment of purified PrPSc with neuraminidase.	n-linked glycans	130-146	prion protein	Mus musculus	124-129
30021839-1	2018	Endoplasmic reticulum (ER) degradation-enhancing alpha-mannosidase-like 1 protein (EDEM1) is a protein quality control factor that was initially proposed to recognize N-linked glycans on misfolded proteins through its mannosidase-like domain (MLD).	n-linked glycans	167-183	ER degradation enhancing alpha-mannosidase like protein 1	Homo sapiens	0-73
30021839-1	2018	Endoplasmic reticulum (ER) degradation-enhancing alpha-mannosidase-like 1 protein (EDEM1) is a protein quality control factor that was initially proposed to recognize N-linked glycans on misfolded proteins through its mannosidase-like domain (MLD).	n-linked glycans	167-183	ER degradation enhancing alpha-mannosidase like protein 1	Homo sapiens	83-88
29983388-2	2018	We have found an unexplored mechanism, by which basic fibroblast growth factor (FGF2) induces expression of fucosyltransferase 8 (FUT8) to increase core fucosylations of N-linked glycans of membrane-associated proteins, including several integrin subunits.	n-linked glycans	170-186	fibroblast growth factor 2	Homo sapiens	80-84
29983388-2	2018	We have found an unexplored mechanism, by which basic fibroblast growth factor (FGF2) induces expression of fucosyltransferase 8 (FUT8) to increase core fucosylations of N-linked glycans of membrane-associated proteins, including several integrin subunits.	n-linked glycans	170-186	fucosyltransferase 8	Homo sapiens	108-128
29983388-2	2018	We have found an unexplored mechanism, by which basic fibroblast growth factor (FGF2) induces expression of fucosyltransferase 8 (FUT8) to increase core fucosylations of N-linked glycans of membrane-associated proteins, including several integrin subunits.	n-linked glycans	170-186	fucosyltransferase 8	Homo sapiens	130-134
30054538-9	2018	To test whether the microglial response is mediated by carbohydrate epitopes on PrPSc surface, the levels of sialylation of PrPSc N-linked glycans was altered by treatment of purified PrPSc with neuraminidase.	n-linked glycans	130-146	prion protein	Mus musculus	124-129
29575162-4	2018	N-linked glycans are first released from glycoproteins by enzymatic digestion, then labeled with fluorescence dyes for subsequent CE or LC separation, and LIF or MS detection.	n-linked glycans	0-16	LIF interleukin 6 family cytokine	Homo sapiens	155-158
29575162-8	2018	CONCLUSIONS: This on-line CE/LIF/MS method using Teal  fluorescent dye and electrokinetic pump-based nanospray sheath liquid CE/MS coupling technology holds promise for on-line quantitation and identification of N-linked glycans on recombinant therapeutic proteins.	n-linked glycans	212-228	LIF interleukin 6 family cytokine	Homo sapiens	29-32
29858715-6	2018	PIP carries unusual highly fucosylated N-linked glycans with multiple Lewisy (Ley) epitopes on bi-, tri- and tetraantennary structures resulting in up to nine fucosyl residues on a tetraantennary glycan.	n-linked glycans	39-55	prolactin induced protein	Homo sapiens	0-3
29760474-0	2018	Structural basis for the recognition of complex-type N-glycans by Endoglycosidase S. Endoglycosidase S (EndoS) is a bacterial endo-beta-N-acetylglucosaminidase that specifically catalyzes the hydrolysis of the beta-1,4 linkage between the first two N-acetylglucosamine residues of the biantennary complex-type N-linked glycans of IgG Fc regions.	n-linked glycans	310-326	O-GlcNAcase	Homo sapiens	131-159
29579062-11	2018	Overall, our data demonstrate that HIV-1 isolates display differential sensitivity to lectins, in part due to the microheterogeneity of N-linked glycans expressed on the surface of the virus Env glycoprotein.	n-linked glycans	136-152	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	191-194
29273674-0	2018	Alternative routes for synthesis of N-linked glycans by Alg2 mannosyltransferase.	n-linked glycans	36-52	GDP-Man:Man(1)GlcNAc(2)-PP-dolichol alpha-1,3-mannosyltransferase	Saccharomyces cerevisiae S288C	56-60
29706962-1	2018	Immunoglobulin G (IgG) can contain N-linked glycans in the variable domains, the so-called Fab glycans, in addition to the Fc glycans in the CH2 domains.	n-linked glycans	35-51	FA complementation group B	Homo sapiens	91-94
29187368-0	2018	N-linked glycans are required on epithelial Na+ channel subunits for maturation and surface expression.	n-linked glycans	0-16	sodium channel epithelial 1 subunit gamma	Rattus norvegicus	33-55
29548671-3	2018	The crystal structure of the antigen-binding fragment of VRC-PG05 in complex with gp120 revealed an epitope comprised primarily of N-linked glycans from N262, N295, and N448 at the silent face center.	n-linked glycans	131-147	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	82-87
29187368-4	2018	Heterologous expression in Xenopus oocytes or Fischer rat thyroid cells with alphabetagamma-ENaC lacking N-linked glycans on a single subunit reduced ENaC activity as well as the inhibitory response to extracellular Na+.	n-linked glycans	105-121	sodium channel epithelial 1 subunit gamma	Rattus norvegicus	92-96
29187368-4	2018	Heterologous expression in Xenopus oocytes or Fischer rat thyroid cells with alphabetagamma-ENaC lacking N-linked glycans on a single subunit reduced ENaC activity as well as the inhibitory response to extracellular Na+.	n-linked glycans	105-121	sodium channel epithelial 1 subunit gamma	Rattus norvegicus	150-154
28632942-1	2017	N-linked glycans such as 234 and 276 gp120 glycans are vital components of HIV evasion from humoral immunity and important for HIV-1 neutralization of many broadly neutralizing antibodies (bNAbs).	n-linked glycans	0-16	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	37-42
29324290-2	2018	As MBL binds to carbohydrates, we hypothesized that N-linked glycans on the RRV envelope glycoproteins act as ligands for MBL.	n-linked glycans	52-68	mannose binding lectin 2	Homo sapiens	3-6
29324290-2	2018	As MBL binds to carbohydrates, we hypothesized that N-linked glycans on the RRV envelope glycoproteins act as ligands for MBL.	n-linked glycans	52-68	mannose binding lectin 2	Homo sapiens	122-125
29324290-3	2018	Using a panel of RRV mutants lacking the envelope N-linked glycans, we found that MBL deposition onto infected cells was dependent on the E2 glycans.	n-linked glycans	50-66	mannose binding lectin 2	Homo sapiens	82-85
29324290-6	2018	These results demonstrate that the viral N-linked glycans promote MBL deposition and complement activation onto RRV-infected cells, contributing to the development of RRV-induced myositis.	n-linked glycans	41-57	mannose binding lectin 2	Homo sapiens	66-69
28472687-5	2017	Glycan array analysis of DBL revealed its affinity toward high mannose N-linked glycans with enhanced affinity for terminal mannose including N-linked glycans of HIV envelope glycoprotein gp120 and has strong anti-reverse transcriptase activity.	n-linked glycans	71-87	MCF.2 cell line derived transforming sequence	Homo sapiens	25-28
28803068-4	2017	Hydrophilic Interaction Liquid Chromatography determined the structure of N-linked glycans present in HEK293-expressed hIFNgamma (hIFNgamma-HEK).	n-linked glycans	74-90	interferon gamma	Homo sapiens	119-128
28803068-4	2017	Hydrophilic Interaction Liquid Chromatography determined the structure of N-linked glycans present in HEK293-expressed hIFNgamma (hIFNgamma-HEK).	n-linked glycans	74-90	interferon gamma	Homo sapiens	130-139
28679530-1	2017	To study how the interaction between N-linked glycans and the surrounding amino acids influences oligosaccharide processing, we used protein disulfide isomerase (PDI), a glycoprotein bearing 5 N-glycosylation sites, as a model system and expressed it transiently in a Chinese hamster ovary (CHO)-S cell line.	n-linked glycans	37-53	protein disulfide-isomerase	Cricetulus griseus	162-165
28389847-8	2017	Our data provide pivotal information to distinguish between HBV-associated hepatitis, cirrhosis and HCC, and facilitate the discovery of biomarkers for HCC during its early stages based on precise alterations of N-linked glycans in saliva.	n-linked glycans	212-228	HCC	Homo sapiens	152-155
28160363-1	2017	Plant-produced glycoproteins contain N-linked glycans with plant-specific residues of beta(1,2)-xylose and core alpha(1,3)-fucose, which do not exist in mammalian-derived proteins.	n-linked glycans	37-53	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	86-94
28364041-7	2017	Moreover, galectin-3 bound to N-linked glycans on CD146 and induced CD146 dimerization and subsequent activation of AKT signaling.	n-linked glycans	30-46	galectin 3	Homo sapiens	10-20
28370891-6	2017	ADAMTS-13 contains 10 N-linked glycans, with four sites present in theTSP2 through to CUB domains that may contribute to its conformation.	n-linked glycans	22-38	ADAM metallopeptidase with thrombospondin type 1 motif 13	Homo sapiens	0-9
28370891-15	2017	Immunoprecipitation experiments confirmed that loss of N-linked glycans in the CUB domains significantly reduced the interaction with the spacer domain and enhanced binding to the 6A6 anti-ADAMTS-13 antibody, which recognizes a cryptic epitope in the metalloprotease domain.	n-linked glycans	55-71	ADAM metallopeptidase with thrombospondin type 1 motif 13	Homo sapiens	189-198
28370891-16	2017	Conclusions Together, these data demonstrate that the N-linked glycans of ADAMTS-13 play a crucial role in regulating ADAMTS-13 activity.	n-linked glycans	54-70	ADAM metallopeptidase with thrombospondin type 1 motif 13	Homo sapiens	74-83
28370891-16	2017	Conclusions Together, these data demonstrate that the N-linked glycans of ADAMTS-13 play a crucial role in regulating ADAMTS-13 activity.	n-linked glycans	54-70	ADAM metallopeptidase with thrombospondin type 1 motif 13	Homo sapiens	118-127
28424265-11	2017	Notably, N-linked glycans produced by GNE-deficient cells displayed enhanced binding to galectin-1, indicating that changes in GNE activity can alter affinity of cell-surface glycoproteins for the galectin lattice.	n-linked glycans	9-25	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	Homo sapiens	38-41
28424265-11	2017	Notably, N-linked glycans produced by GNE-deficient cells displayed enhanced binding to galectin-1, indicating that changes in GNE activity can alter affinity of cell-surface glycoproteins for the galectin lattice.	n-linked glycans	9-25	galectin 1	Homo sapiens	88-98
28424265-11	2017	Notably, N-linked glycans produced by GNE-deficient cells displayed enhanced binding to galectin-1, indicating that changes in GNE activity can alter affinity of cell-surface glycoproteins for the galectin lattice.	n-linked glycans	9-25	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	Homo sapiens	127-130
28364041-7	2017	Moreover, galectin-3 bound to N-linked glycans on CD146 and induced CD146 dimerization and subsequent activation of AKT signaling.	n-linked glycans	30-46	melanoma cell adhesion molecule	Homo sapiens	50-55
28323990-9	2017	Results: We analyzed N-linked glycans and glycolipids in knockout TMEM165 HEK293 cells, revealing severe hypogalactosylation and GalNAc transfer defects.	n-linked glycans	21-37	transmembrane protein 165	Homo sapiens	66-73
27888602-6	2017	Moreover, treatment with the alpha(1,3)-fucosyltransferase-FTVII also generated expression of HCELL on both BM-hMSCs and A-hMSCs, with sLeX decorations created on N-linked glycans of the "standard" CD44 (CD44s) isoform.	n-linked glycans	163-179	fucosyltransferase 7	Homo sapiens	29-58
28207759-3	2017	Supplementing storage cells with lacking enzyme is accomplished via chronic intravenous administration of recombinant GBA containing mannose-terminated N-linked glycans, mediating the selective uptake by macrophages expressing mannose-binding lectin(s).	n-linked glycans	152-168	glucosylceramidase beta	Homo sapiens	118-121
28207759-3	2017	Supplementing storage cells with lacking enzyme is accomplished via chronic intravenous administration of recombinant GBA containing mannose-terminated N-linked glycans, mediating the selective uptake by macrophages expressing mannose-binding lectin(s).	n-linked glycans	152-168	mannose binding lectin 2	Homo sapiens	227-249
28207759-4	2017	Two recombinant GBA preparations with distinct N-linked glycans are registered in Europe for treatment of type I GD: imiglucerase (Genzyme), contains predominantly Man(3) glycans, and velaglucerase (Shire PLC) Man(9) glycans.	n-linked glycans	47-63	glucosylceramidase beta	Homo sapiens	16-19
28031460-4	2017	We found that a gene encoding beta-galactoside alpha2,6-sialyltransferase-1 (St6gal1), a key enzyme responsible for the biosynthesis of alpha2,6-linked sialic acid in N-linked glycans, was most down-regulated in VATs from obese mice.	n-linked glycans	167-183	beta galactoside alpha 2,6 sialyltransferase 1	Mus musculus	30-75
27956708-1	2017	Recently, we showed the unexpectedly high abundance of N-linked glycans on the Fab-domain of Anti-Citrullinated Protein Antibodies (ACPA).	n-linked glycans	55-71	FA complementation group B	Homo sapiens	79-82
28148964-5	2017	Mitochondrial PrPC was fully processed with mature N-linked glycans and did not require the GPI anchor for localization.	n-linked glycans	51-67	prion protein	Mus musculus	14-18
27490136-2	2017	Owing to their alpha-1,2 mannosidase activity, the EDEM1-3 proteins are able to process the N-linked glycans of misfolded or incompletely folded proteins, providing the recognition signal for their subsequent degradation.	n-linked glycans	92-108	mannosidase alpha class 1A member 2	Homo sapiens	15-36
27490136-2	2017	Owing to their alpha-1,2 mannosidase activity, the EDEM1-3 proteins are able to process the N-linked glycans of misfolded or incompletely folded proteins, providing the recognition signal for their subsequent degradation.	n-linked glycans	92-108	ER degradation enhancing alpha-mannosidase like protein 1	Homo sapiens	51-56
28031460-4	2017	We found that a gene encoding beta-galactoside alpha2,6-sialyltransferase-1 (St6gal1), a key enzyme responsible for the biosynthesis of alpha2,6-linked sialic acid in N-linked glycans, was most down-regulated in VATs from obese mice.	n-linked glycans	167-183	beta galactoside alpha 2,6 sialyltransferase 1	Mus musculus	77-84
28031460-4	2017	We found that a gene encoding beta-galactoside alpha2,6-sialyltransferase-1 (St6gal1), a key enzyme responsible for the biosynthesis of alpha2,6-linked sialic acid in N-linked glycans, was most down-regulated in VATs from obese mice.	n-linked glycans	167-183	gamma-aminobutyric acid (GABA) A receptor, subunit alpha 6	Mus musculus	47-55
27956708-1	2017	Recently, we showed the unexpectedly high abundance of N-linked glycans on the Fab-domain of Anti-Citrullinated Protein Antibodies (ACPA).	n-linked glycans	55-71	proteinase 3	Homo sapiens	93-130
27956708-1	2017	Recently, we showed the unexpectedly high abundance of N-linked glycans on the Fab-domain of Anti-Citrullinated Protein Antibodies (ACPA).	n-linked glycans	55-71	proteinase 3	Homo sapiens	132-136
27956708-2	2017	As N-linked glycans can mediate a variety of biological functions, we now aimed at investigating the structural composition of the Fab-glycans of ACPA-IgG to better understand their mediated biological effects.	n-linked glycans	3-19	proteinase 3	Homo sapiens	146-150
27707925-1	2016	The HIV envelope glycoprotein (Env) is extensively modified with host-derived N-linked glycans.	n-linked glycans	78-94	endogenous retrovirus group K member 20	Homo sapiens	8-29
27561202-1	2016	The hormone - specific FSHbeta subunit of the human FSH heterodimer consists of N-linked glycans at Asn7 and Asn24 residues that are co-translationally attached early during subunit biosynthesis.	n-linked glycans	80-96	follicle stimulating hormone subunit beta	Homo sapiens	23-30
27834568-6	2017	Removal of the Fab N-glycosylation site by single amino acid substitution, or removal of N-linked glycans by enzymatic digestion, drastically reduced the antibody"s ability to inhibit latency-associated peptide (LAP) and alphavbeta8 association, and TGF-beta activation in an alphavbeta8-mediated TGF-beta signaling reporter assay.	n-linked glycans	89-105	transforming growth factor beta 1	Homo sapiens	184-210
27834568-6	2017	Removal of the Fab N-glycosylation site by single amino acid substitution, or removal of N-linked glycans by enzymatic digestion, drastically reduced the antibody"s ability to inhibit latency-associated peptide (LAP) and alphavbeta8 association, and TGF-beta activation in an alphavbeta8-mediated TGF-beta signaling reporter assay.	n-linked glycans	89-105	transforming growth factor beta 1	Homo sapiens	212-215
27707925-1	2016	The HIV envelope glycoprotein (Env) is extensively modified with host-derived N-linked glycans.	n-linked glycans	78-94	endogenous retrovirus group K member 20	Homo sapiens	31-34
27707925-11	2016	The HIV envelope glycoprotein (Env) is covered in an array of host-derived N-linked glycans often referred to as the glycan shield.	n-linked glycans	75-91	endogenous retrovirus group K member 20	Homo sapiens	8-29
27707925-11	2016	The HIV envelope glycoprotein (Env) is covered in an array of host-derived N-linked glycans often referred to as the glycan shield.	n-linked glycans	75-91	endogenous retrovirus group K member 20	Homo sapiens	31-34
27554083-0	2016	N-linked glycans within the A2 domain of von Willebrand factor modulate macrophage-mediated clearance.	n-linked glycans	0-16	von Willebrand factor	Homo sapiens	41-62
26960182-6	2016	Binding of Abs to epithelial cells was diminished following MUC16 knockdown, and the MUC16 N-linked glycans were critical for binding.	n-linked glycans	91-107	mucin 16, cell surface associated	Homo sapiens	85-90
27798151-5	2016	Unlike mammalian cell-derived NS1, which displays both high mannose and complex type N-linked glycans, soluble NS1 secreted from DENV-infected insect cells contains only high mannose glycans.	n-linked glycans	85-101	influenza virus NS1A binding protein	Homo sapiens	30-33
27554083-6	2016	Previous studies have demonstrated that the N-linked glycans within the A2 domain play an important role in modulating susceptibility to ADAMTS13 proteolysis.	n-linked glycans	44-60	ADAM metallopeptidase with thrombospondin type 1 motif 13	Homo sapiens	137-145
27316967-7	2016	The findings indicate that the growth of S. gordonii DL1 in saliva depends to a significant extent on the sequential actions of first BgaA and then StrH and EndoD on N-linked glycans of PRG.	n-linked glycans	166-182	Galactose-specific C-type lectin	Drosophila melanogaster	53-56
27607237-3	2016	Here, we identified and characterized MoGls2 in Magnaporthe oryzae, which is a yeast glucosidase II homolog Gls2 and is required for trimming the final glucose in N-linked glycans and normal cell wall synthesis.	n-linked glycans	163-179	glucan 1,3-alpha-glucosidase ROT2	Saccharomyces cerevisiae S288C	40-44
26829466-6	2016	Tsg has a high proportion of N-linked glycans, in relation to its molecular weight, which supports a role in solubilising BMPs.	n-linked glycans	29-45	twisted gastrulation BMP signaling modulator 1	Homo sapiens	0-3
27489265-11	2016	IMPORTANCE: The HIV-1 Env glycoprotein presents a dense patchwork of host cell-derived N-linked glycans.	n-linked glycans	87-103	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	22-25
27316967-12	2016	The results indicate that the growth of S. gordonii DL1 depends to a significant extent on sequential action of these cell surface GHs on N-linked glycans of basic proline-rich salivary glycoproteins, which appears to be an essential first step in salivary glycan foraging.	n-linked glycans	138-154	Galactose-specific C-type lectin	Drosophila melanogaster	52-55
27006333-1	2016	Whether the two N-linked glycans are important in prion, PrP, biology is unresolved.	n-linked glycans	16-32	major prion protein	Cricetulus griseus	57-60
27317661-1	2016	Prions or PrP(Sc) are proteinaceous infectious agents that consist of misfolded, self-replicating states of the prion protein or PrP(C) PrP(C) is posttranslationally modified with N-linked glycans and a sialylated glycosylphosphatidylinositol (GPI) anchor.	n-linked glycans	180-196	prion protein	Mus musculus	10-13
27281343-3	2016	We have previously reported that mature ABCC11 is a glycoprotein containing two N-linked glycans at Asn838 and Asn844.	n-linked glycans	80-96	ATP binding cassette subfamily C member 11	Homo sapiens	40-46
27222580-9	2016	N-linked glycans and carbohydrate-binding molecular chaperones contribute to the efficient folding and secretion of functional ATIII.	n-linked glycans	0-16	serpin family C member 1	Homo sapiens	127-132
26911932-11	2016	Our genetic approach provides direct in vivo evidence that N-linked glycans on FSHbeta subunit are essential for its efficient assembly with the alpha-subunit to form FSH heterodimer in pituitary.	n-linked glycans	59-75	follicle stimulating hormone beta	Mus musculus	79-86
27084007-3	2016	Recently, a cell wall-associated endo-beta-N-acetylglucosaminidase (EndoBI-1) found in various infant-borne bifidobacteria was shown to remove a range of intact N-linked glycans.	n-linked glycans	161-177	O-GlcNAcase	Homo sapiens	38-66
27013611-4	2016	Exoglycosidase removal of FVIII N-linked glycans significantly reduced binding to both Gal-1 and Gal-3.	n-linked glycans	32-48	coagulation factor VIII	Homo sapiens	26-31
27013611-4	2016	Exoglycosidase removal of FVIII N-linked glycans significantly reduced binding to both Gal-1 and Gal-3.	n-linked glycans	32-48	galectin 1	Homo sapiens	87-92
27013611-4	2016	Exoglycosidase removal of FVIII N-linked glycans significantly reduced binding to both Gal-1 and Gal-3.	n-linked glycans	32-48	galectin 3	Homo sapiens	97-102
26503547-1	2016	The acquisition of mannose 6-phosphate (Man6P) on N-linked glycans of lysosomal enzymes is a structural requirement for their transport from the Golgi apparatus to lysosomes mediated by the mannose 6-phosphate receptors, 300 kDa cation-independent mannose 6-phosphate receptor (MPR300) and 46 kDa cation-dependent mannose 6-phosphate receptor (MPR46).	n-linked glycans	50-66	insulin like growth factor 2 receptor	Homo sapiens	278-284
26773038-4	2016	We investigated how the N-linked glycans of the VWF A2 domain affect thermostability and regulate both the exposure of the ADAMTS13 binding sites and the scissile bond.	n-linked glycans	24-40	von Willebrand factor	Homo sapiens	48-51
26773038-4	2016	We investigated how the N-linked glycans of the VWF A2 domain affect thermostability and regulate both the exposure of the ADAMTS13 binding sites and the scissile bond.	n-linked glycans	24-40	ADAM metallopeptidase with thrombospondin type 1 motif 13	Homo sapiens	123-131
26773038-5	2016	We show by differential scanning fluorimetry that the N-linked glycans thermodynamically stabilize the VWF A2 domain.	n-linked glycans	54-70	von Willebrand factor	Homo sapiens	103-106
26972002-1	2016	The HIV-1 envelope glycoprotein trimer is covered by an array of N-linked glycans that shield it from immune surveillance.	n-linked glycans	65-81	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	10-31
26503547-1	2016	The acquisition of mannose 6-phosphate (Man6P) on N-linked glycans of lysosomal enzymes is a structural requirement for their transport from the Golgi apparatus to lysosomes mediated by the mannose 6-phosphate receptors, 300 kDa cation-independent mannose 6-phosphate receptor (MPR300) and 46 kDa cation-dependent mannose 6-phosphate receptor (MPR46).	n-linked glycans	50-66	mannose-6-phosphate receptor, cation dependent	Homo sapiens	297-342
26503547-1	2016	The acquisition of mannose 6-phosphate (Man6P) on N-linked glycans of lysosomal enzymes is a structural requirement for their transport from the Golgi apparatus to lysosomes mediated by the mannose 6-phosphate receptors, 300 kDa cation-independent mannose 6-phosphate receptor (MPR300) and 46 kDa cation-dependent mannose 6-phosphate receptor (MPR46).	n-linked glycans	50-66	mannose-6-phosphate receptor, cation dependent	Homo sapiens	344-349
26630650-6	2015	Two complex N-linked glycans akin to honey bee hyaluronidase glycosylations, were identified by tandem mass spectrometry.	n-linked glycans	12-28	hyaluronidase	Apis mellifera	47-60
26411545-2	2015	HIV Env is one of the most heavily glycosylated proteins known, with approximately half of its mass consisting of host-derived N-linked glycans.	n-linked glycans	127-143	endogenous retrovirus group K member 20	Homo sapiens	4-7
26039217-10	2015	These data identify roles for ankyrin domain-4, cell surface N-linked glycans, and selected pore-loop domain residues in the activation of TRPA1 by insoluble particles.	n-linked glycans	61-77	transient receptor potential cation channel subfamily A member 1	Homo sapiens	139-144
26296369-5	2015	In agreement, the glycomics analysis determines the glycosylation site and the N-glycan composition of CD69, and terminal removal of sialic acid from that N-linked glycans reverses the generation of forkhead box P3-positive Treg cells (23.21%; P < 0.05).	n-linked glycans	155-171	CD69 molecule	Homo sapiens	103-107
26085151-1	2015	UNLABELLED: The gp120/gp41 HIV-1 envelope glycoprotein (Env) is highly glycosylated, with up to 50% of its mass consisting of N-linked glycans.	n-linked glycans	126-142	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	16-21
25630622-1	2015	PURPOSE: beta1,6-N-acetylglucosaminyltransferase V (MGAT5), which is required for the biosynthesis of beta1,6GlcNAc-branched N-linked glycans attached to cell surface and secreted glycoproteins, accounts for oncogenic growth signal transduction during the development and progression of various malignancies.	n-linked glycans	125-141	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B	Homo sapiens	9-50
25630622-1	2015	PURPOSE: beta1,6-N-acetylglucosaminyltransferase V (MGAT5), which is required for the biosynthesis of beta1,6GlcNAc-branched N-linked glycans attached to cell surface and secreted glycoproteins, accounts for oncogenic growth signal transduction during the development and progression of various malignancies.	n-linked glycans	125-141	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	52-57
26277072-1	2015	The glycan shield on the human immunodeficiency virus 1 (HIV-1) envelope (Env) glycoprotein has drawn attention as a target for HIV-1 vaccine design given that an increasing number of potent and broadly neutralizing antibodies (bNAbs) recognize epitopes entirely or partially comprised of high mannose type N-linked glycans.	n-linked glycans	307-323	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	74-77
26203194-3	2015	The two N-linked glycans and the C-terminal domain that attach the core protein to the cell membrane are not resolved in the Gpc1 crystal structure.	n-linked glycans	8-24	glypican 1	Homo sapiens	125-129
26148749-0	2015	Lectins as probes for assessing the accessibility of N-linked glycans in relation to the conformational changes of fibronectin.	n-linked glycans	53-69	fibronectin 1	Homo sapiens	115-126
26085151-1	2015	UNLABELLED: The gp120/gp41 HIV-1 envelope glycoprotein (Env) is highly glycosylated, with up to 50% of its mass consisting of N-linked glycans.	n-linked glycans	126-142	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	33-54
26085151-1	2015	UNLABELLED: The gp120/gp41 HIV-1 envelope glycoprotein (Env) is highly glycosylated, with up to 50% of its mass consisting of N-linked glycans.	n-linked glycans	126-142	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	56-59
26085151-11	2015	Increasingly, HIV bnAbs are being identified that bind to the N-linked glycans coating the HIV envelope glycoproteins gp120 and gp41, highlighting them as important targets for vaccine design.	n-linked glycans	62-78	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	118-123
26271046-3	2015	To date, a unique trisaccharide (HSO3-3GlcAbeta1-3Galbeta1-4GlcNAc), human natural killer-1 (HNK-1) carbohydrate, was found expressed specifically on N-linked glycans of GluA2 and regulated the cell surface expression of AMPAR and the spine maturation process.	n-linked glycans	150-166	beta-1,3-glucuronyltransferase 1	Homo sapiens	93-98
26291458-7	2015	Smo proteins in Drosophila and vertebrate systems harbor N-linked glycans, but their role in Smo signaling has not been established.	n-linked glycans	57-73	smoothened	Drosophila melanogaster	0-3
26291458-8	2015	Herein, we present a comprehensive analysis of Drosophila and murine Smo glycosylation that supports a functional divergence in the contribution of N-linked glycans to signaling.	n-linked glycans	148-164	smoothened, frizzled class receptor	Mus musculus	69-72
25995448-3	2015	The C-type carbohydrate recognition domain in the extracellular portion of BDCA-2 contains a signature motif typical of C-type animal lectins that bind mannose, glucose, or GlcNAc, yet it has been reported that BDCA-2 binds selectively to galactose-terminated, biantennary N-linked glycans.	n-linked glycans	273-289	C-type lectin domain family 4 member C	Homo sapiens	75-81
25995448-3	2015	The C-type carbohydrate recognition domain in the extracellular portion of BDCA-2 contains a signature motif typical of C-type animal lectins that bind mannose, glucose, or GlcNAc, yet it has been reported that BDCA-2 binds selectively to galactose-terminated, biantennary N-linked glycans.	n-linked glycans	273-289	C-type lectin domain family 4 member C	Homo sapiens	211-217
25827571-9	2015	Importantly, most of the novel Sppl3 substrates catalyze the modification of N-linked glycans.	n-linked glycans	77-93	signal peptide peptidase like 3	Homo sapiens	31-36
26121645-1	2015	The HIV envelope glycoprotein gp120 contains nine disulphide bridges and is highly glycosylated, carrying on average 24 N-linked glycans.	n-linked glycans	120-136	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	30-35
26121645-2	2015	Using a probability calculation, we here demonstrate that there is a co-localization of disulphide bridges and N-linked glycans in HIV-1 gp120, with a predominance of N-linked glycans in close proximity to disulphide bridges, at the C-terminal side of the involved cysteines.	n-linked glycans	111-127	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	137-142
26121645-2	2015	Using a probability calculation, we here demonstrate that there is a co-localization of disulphide bridges and N-linked glycans in HIV-1 gp120, with a predominance of N-linked glycans in close proximity to disulphide bridges, at the C-terminal side of the involved cysteines.	n-linked glycans	167-183	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	137-142
25546301-1	2015	The crystal structure of a fully glycosylated HIV-1 gp120 core in complex with CD4 receptor and Fab 17b at 4.5-A resolution reveals 9 of the 15 N-linked glycans of core gp120 to be partially ordered.	n-linked glycans	144-160	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	52-57
25546301-1	2015	The crystal structure of a fully glycosylated HIV-1 gp120 core in complex with CD4 receptor and Fab 17b at 4.5-A resolution reveals 9 of the 15 N-linked glycans of core gp120 to be partially ordered.	n-linked glycans	144-160	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	169-174
25293322-5	2015	Upon deglycosylation to remove N-linked glycans by PNGase F (but not Endo H), the MOPR became a dense and sharp band with Mr of ~43 kDa, close to the theoretical Mr of its deduced amino acid sequences.	n-linked glycans	31-47	opioid receptor, mu 1	Mus musculus	82-86
25304981-4	2015	N-linked glycans in the IGF receptor, IGF1R, influence its presentation at the cell surface.	n-linked glycans	0-16	insulin like growth factor 1 receptor	Homo sapiens	38-43
25304981-7	2015	Decreased binding of Phaseolus vulgaris lectin and phytohaemagglutinin to IGF1R immunoprecipitated from treated explants demonstrated reduced levels of complex N-linked glycans.	n-linked glycans	160-176	insulin like growth factor 1 receptor	Homo sapiens	74-79
25499264-2	2014	The development of phenotypic resistance to CBAs by the virus is accompanied by the deletion of multiple N-linked glycans of the surface envelope glycoprotein gp120.	n-linked glycans	105-121	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	159-164
24967714-1	2014	N-linked glycans covering the surface of the HIV-1 glycoprotein gp120 are of major importance for the correct folding of this glycoprotein.	n-linked glycans	0-16	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	64-69
25658012-0	2014	Retraction notice to NKR-P1A protein, an activating receptor of rat natural killer cells, binds to the chitobiose core of uncompletely glycosylated N-linked glycans, and to linear chitooligomers [Biochem.	n-linked glycans	148-164	killer cell lectin-like receptor subfamily B, member 1A	Rattus norvegicus	21-28
25658013-0	2014	Retraction notice to RETRACTED: NKR-P1A protein, an activating receptor of rat natural killer cells, binds to the chitobiose core of uncompletely glycosylated N-linked glycans, and to linear chitooligomers [Biochem.	n-linked glycans	159-175	killer cell lectin-like receptor subfamily B, member 1A	Rattus norvegicus	32-39
24965454-2	2014	2G12 is a unique, domain-exchanged antibody that binds exclusively to conserved N-linked glycans that form the high-mannose patch on the gp120 outer domain centered on a glycan at position N332.	n-linked glycans	80-96	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	137-142
24992528-9	2014	Essential elements of the glycan V3 supersite, embodied by as few as 3 N-linked glycans and ~ 25 Env residues, can be segregated into acceptor scaffolds away from the immune-evading capabilities of the rest of HIV-1 Env, thereby providing a means to focus the immune response on the scaffolded supersite.	n-linked glycans	71-87	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	216-219
24934233-4	2014	Additionally, mouse interleukin-3 expressed by a recombinant BmNPV was normally secreted and modified with N-linked glycans in BmN-SFM cells.	n-linked glycans	107-123	interleukin 3	Mus musculus	20-33
25014350-2	2014	Previous studies have demonstrated that the native GP5 glycoprotein is poorly immunogenic and not able to induce robust protective responses, probably due to the presence of a non-neutralizing decoy epitope and shielding N-linked glycans close to its neutralizing epitope.	n-linked glycans	221-237	glycoprotein V platelet	Homo sapiens	51-54
24884609-9	2014	Site N274 contained high-mannose N-linked glycans in both serum and recombinant ITIH4.	n-linked glycans	33-49	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	80-85
24967714-2	2014	Of the, on average, 24 N-linked glycans present on gp120, the glycan at Asn260 was reported to be essential for the correct expression of gp120 and gp41 in the virus particle and deletion of the N260 glycan in gp120 heavily compromised virus infectivity.	n-linked glycans	23-39	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	51-56
24303005-0	2013	The influence of N-linked glycans on the molecular dynamics of the HIV-1 gp120 V3 loop.	n-linked glycans	17-33	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	73-78
24213971-0	2014	Co-expression of gamma2 subunits hinders processing of N-linked glycans attached to the N104 glycosylation sites of GABAA receptor beta2 subunits.	n-linked glycans	55-71	tryptophanyl-tRNA synthetase 1	Homo sapiens	17-23
24213971-0	2014	Co-expression of gamma2 subunits hinders processing of N-linked glycans attached to the N104 glycosylation sites of GABAA receptor beta2 subunits.	n-linked glycans	55-71	potassium calcium-activated channel subfamily M regulatory beta subunit 2	Homo sapiens	131-136
24336949-3	2014	In this study, we examined the role that N-linked glycans (NLG) play in the secretion of BMP-2.	n-linked glycans	41-57	bone morphogenetic protein 2	Homo sapiens	89-94
24473128-0	2014	Comprehensive functional analysis of N-linked glycans on Ebola virus GP1.	n-linked glycans	37-53	GTP binding protein 1	Mus musculus	69-72
24473128-8	2014	The effects of the loss of GP1 N-linked glycans on Ca(2+)-dependent (C-type) lectin (CLEC)-dependent transduction were complex, and the effect was unique for each of the CLECs tested.	n-linked glycans	31-47	GTP binding protein 1	Mus musculus	27-30
24473128-11	2014	In total, our results provide evidence that the conserved N-linked glycans on the EBOV GP1 core protect GP from antibody neutralization despite the negative impact the glycans have on viral entry efficiency.	n-linked glycans	58-74	GTP binding protein 1	Mus musculus	87-90
24628331-4	2014	A total of 14 unique N-linked glycans corresponding to 27 unique N-linked glycopeptides were characterized at three N-linked sites (Asn-86, -169, and -242) present in VTN.	n-linked glycans	21-37	vitronectin	Homo sapiens	167-170
24608122-3	2014	The identified endo-beta-N-acetylglucosaminidase EndoE has activity on the N-linked glycans of the human immunoglobulin G (IgG).	n-linked glycans	75-91	O-GlcNAcase	Homo sapiens	20-48
24357164-1	2014	Human glycodelin consists of 162 amino acid residues and two N-linked glycans at Asn(28) and Asn(63) .	n-linked glycans	61-77	progestagen associated endometrial protein	Homo sapiens	6-16
24282309-4	2013	The cystine knot of Spz binds the concave face of the Toll leucine-rich repeat solenoid in an area delineated by N-linked glycans and induces a conformational change.	n-linked glycans	113-129	spatzle	Drosophila melanogaster	20-23
24282309-4	2013	The cystine knot of Spz binds the concave face of the Toll leucine-rich repeat solenoid in an area delineated by N-linked glycans and induces a conformational change.	n-linked glycans	113-129	Toll	Drosophila melanogaster	54-58
24115046-4	2013	Almost all of the N-linked glycans in human LCAT are fucosylated and sialylated.	n-linked glycans	18-34	lecithin-cholesterol acyltransferase	Homo sapiens	44-48
24224757-2	2013	Interactions of SP-D with highly branched viral N-linked glycans on hemagglutinin (HA), an abundant IAV envelope protein and critical virulence factor, promote viral aggregation and neutralization through as yet unknown molecular mechanisms.	n-linked glycans	48-64	surfactant protein D	Homo sapiens	16-20
24303005-1	2013	N-linked glycans attached to specific amino acids of the gp120 envelope trimer of a HIV virion can modulate the binding affinity of gp120 to CD4, influence coreceptor tropism, and play an important role in neutralising antibody responses.	n-linked glycans	0-16	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	57-62
24303005-1	2013	N-linked glycans attached to specific amino acids of the gp120 envelope trimer of a HIV virion can modulate the binding affinity of gp120 to CD4, influence coreceptor tropism, and play an important role in neutralising antibody responses.	n-linked glycans	0-16	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	132-137
24303005-1	2013	N-linked glycans attached to specific amino acids of the gp120 envelope trimer of a HIV virion can modulate the binding affinity of gp120 to CD4, influence coreceptor tropism, and play an important role in neutralising antibody responses.	n-linked glycans	0-16	CD4 molecule	Homo sapiens	141-144
24303005-3	2013	Here, we use a computational approach to determine the influence of N-linked glycans on the dynamics of the HIV-1 gp120 protein and, in particular, the V3 loop.	n-linked glycans	68-84	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	114-119
24010128-8	2013	The proposed derivatization technique is successfully applied to the profiling of N-linked glycans derived from chicken ovalbumin.	n-linked glycans	82-98	ovalbumin (SERPINB14)	Gallus gallus	120-129
24036269-2	2013	However, factor IX (FIX) variants with additional N-linked glycans ("HG" variants) that were expressed in HKB11 cells showed increased clearance in rat in vivo pharmacokinetic studies relative to FIX variants with no additional glycans.	n-linked glycans	50-66	coagulation factor IX	Homo sapiens	9-18
24130780-1	2013	Fucosyltransferase 8 (FUT8) catalyzes the transfer of alpha1,6-linked fucose to the first N-acetylglucosamine in N-linked glycans (core fucosylation).	n-linked glycans	113-129	fucosyltransferase 8	Homo sapiens	0-20
24130780-1	2013	Fucosyltransferase 8 (FUT8) catalyzes the transfer of alpha1,6-linked fucose to the first N-acetylglucosamine in N-linked glycans (core fucosylation).	n-linked glycans	113-129	fucosyltransferase 8	Homo sapiens	22-26
24033743-7	2013	GGTA1/CMAH knockout pig samples had increased relative amounts of high-mannose, incomplete, and xylosylated N-linked glycans.	n-linked glycans	108-124	N-acetyllactosaminide alpha-1,3-galactosyltransferase	Sus scrofa	0-5
23852824-9	2013	FV and FVIII likely bind LMAN1 through the high-mannose N-linked glycans under the higher Ca2+ conditions in the ER and dissociate in the lower Ca2+ environment of the ER-Golgi intermediate compartment.	n-linked glycans	56-72	coagulation factor VIII	Homo sapiens	7-12
23852824-9	2013	FV and FVIII likely bind LMAN1 through the high-mannose N-linked glycans under the higher Ca2+ conditions in the ER and dissociate in the lower Ca2+ environment of the ER-Golgi intermediate compartment.	n-linked glycans	56-72	lectin, mannose binding 1	Homo sapiens	25-30
23738536-5	2013	BTN was concentrated in the apical membrane in all species examined and contained mature N-linked glycans.	n-linked glycans	89-105	butyrophilin, subfamily 1, member A1	Mus musculus	0-3
24033743-7	2013	GGTA1/CMAH knockout pig samples had increased relative amounts of high-mannose, incomplete, and xylosylated N-linked glycans.	n-linked glycans	108-124	cytidine monophospho-N-acetylneuraminic acid hydroxylase	Sus scrofa	6-10
22610315-6	2012	The interaction between ganglioside GM3, and multi (>3) GlcNAc termini of N-linked glycans of epidermal growth factor receptor (EGFR), has been indicated as the molecular mechanism for the inhibitory effect of GM3 on EGFR activation.	n-linked glycans	77-93	granulocyte macrophage antigen 3	Mus musculus	36-39
23536670-1	2013	Griffithsin, which binds N-linked glycans on gp120 to prevent HIV entry, has the most potent HIV-1 inhibitory activity described for any antiviral lectin and is being developed for topical preexposure prophylaxis.	n-linked glycans	25-41	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	45-50
23274891-2	2013	We hypothesized that loss-of-function HNF1A mutations causal for maturity-onset diabetes of the young (MODY) would display altered fucosylation of N-linked glycans on plasma proteins and that glycan biomarkers could improve the efficiency of a diagnosis of HNF1A-MODY.	n-linked glycans	147-163	HNF1 homeobox A	Homo sapiens	38-43
22544341-3	2013	We analysed the N-linked glycans of L1CAM from different stages of melanoma progression, using high-performance liquid chromatography combined with exoglycosidase sequencing, matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry, and lectin probes.	n-linked glycans	16-32	L1 cell adhesion molecule	Homo sapiens	36-41
23777450-10	2013	Here, we present data for the N-linked glycans present on FcgammaRs produced in NS0 cells, namely, FcgammaRIa, FcgammaRIIa, FcgammaRIIB, FcgammaRIIIa, and FcgammaRIIIb.	n-linked glycans	30-46	Fc receptor, IgG, low affinity IIb	Mus musculus	124-135
23416198-2	2013	The immunosuppressive effects of IVIg are, in part, attributed to terminal alpha2,6-linked sialic acid residues on the N-linked glycans of the IgG Fc (fragment crystallizable) domain.	n-linked glycans	119-135	immunoglobulin heavy variable V1-62	Mus musculus	143-146
22610315-6	2012	The interaction between ganglioside GM3, and multi (>3) GlcNAc termini of N-linked glycans of epidermal growth factor receptor (EGFR), has been indicated as the molecular mechanism for the inhibitory effect of GM3 on EGFR activation.	n-linked glycans	77-93	epidermal growth factor receptor	Mus musculus	97-129
22610315-6	2012	The interaction between ganglioside GM3, and multi (>3) GlcNAc termini of N-linked glycans of epidermal growth factor receptor (EGFR), has been indicated as the molecular mechanism for the inhibitory effect of GM3 on EGFR activation.	n-linked glycans	77-93	epidermal growth factor receptor	Mus musculus	131-135
22610315-6	2012	The interaction between ganglioside GM3, and multi (>3) GlcNAc termini of N-linked glycans of epidermal growth factor receptor (EGFR), has been indicated as the molecular mechanism for the inhibitory effect of GM3 on EGFR activation.	n-linked glycans	77-93	granulocyte macrophage antigen 3	Mus musculus	213-216
22610315-6	2012	The interaction between ganglioside GM3, and multi (>3) GlcNAc termini of N-linked glycans of epidermal growth factor receptor (EGFR), has been indicated as the molecular mechanism for the inhibitory effect of GM3 on EGFR activation.	n-linked glycans	77-93	epidermal growth factor receptor	Mus musculus	220-224
22722937-0	2012	Molecular basis for protein-specific transfer of N-acetylgalactosamine to N-linked glycans by the glycosyltransferases beta1,4-N-acetylgalactosaminyl transferase 3 (beta4GalNAc-T3) and beta4GalNAc-T4.	n-linked glycans	74-90	beta-1,4-N-acetyl-galactosaminyltransferase 3	Homo sapiens	119-179
22855528-0	2012	Sialylation of N-linked glycans mediates apical delivery of endolyn in MDCK cells via a galectin-9-dependent mechanism.	n-linked glycans	15-31	CD164 molecule	Rattus norvegicus	60-67
22855528-0	2012	Sialylation of N-linked glycans mediates apical delivery of endolyn in MDCK cells via a galectin-9-dependent mechanism.	n-linked glycans	15-31	galectin-9	Canis lupus familiaris	88-98
22715095-4	2012	A paralog of GnT-Vb, N-acetylglucosaminyltransferase (GnT-V), is expressed in many tissues and brain, synthesizing N-linked, beta1,6-branched glycans, but its ability to synthesize O-mannosyl-branched glycans is unknown; conversely, although GnT-Vb can synthesize N-linked glycans in vitro, its contribution to their synthesis in vivo is unknown.	n-linked glycans	264-280	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B	Homo sapiens	13-19
22715095-4	2012	A paralog of GnT-Vb, N-acetylglucosaminyltransferase (GnT-V), is expressed in many tissues and brain, synthesizing N-linked, beta1,6-branched glycans, but its ability to synthesize O-mannosyl-branched glycans is unknown; conversely, although GnT-Vb can synthesize N-linked glycans in vitro, its contribution to their synthesis in vivo is unknown.	n-linked glycans	264-280	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	13-18
22715095-4	2012	A paralog of GnT-Vb, N-acetylglucosaminyltransferase (GnT-V), is expressed in many tissues and brain, synthesizing N-linked, beta1,6-branched glycans, but its ability to synthesize O-mannosyl-branched glycans is unknown; conversely, although GnT-Vb can synthesize N-linked glycans in vitro, its contribution to their synthesis in vivo is unknown.	n-linked glycans	264-280	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B	Homo sapiens	242-248
23023295-5	2012	Moreover, it became evident that the type of linkage of Sia on N-linked glycans was dramatically changed from alpha-2-3 to alpha-2-6, and the expression of alpha-1-2 fucose and type 1 LacNAc structures became clearly apparent, while no such glycan epitopes were detected in fibroblasts.	n-linked glycans	63-79	immunoglobulin binding protein 1	Homo sapiens	123-132
22261557-5	2012	The lectin binding pattern indicates a massive presence of fucose alpha1,2 linked to galactose in O-glycans and smaller quantities of fucose linked alpha1,6 to N-acetylglucosamine in the core of N-linked glycans.	n-linked glycans	195-211	gamma-aminobutyric acid (GABA) A receptor, subunit alpha 6	Mus musculus	148-156
22298023-6	2012	In contrast to O-linked glycans of ZP3 in mice, N-linked glycans of human ZP3 and ZP4 are more relevant for induction of the acrosome reaction.	n-linked glycans	48-64	zona pellucida glycoprotein 3	Homo sapiens	74-77
22722937-0	2012	Molecular basis for protein-specific transfer of N-acetylgalactosamine to N-linked glycans by the glycosyltransferases beta1,4-N-acetylgalactosaminyl transferase 3 (beta4GalNAc-T3) and beta4GalNAc-T4.	n-linked glycans	74-90	beta-1,4-N-acetyl-galactosaminyltransferase 4	Homo sapiens	185-199
22836271-7	2012	Moreover, the IGF-1-mediated mitogenic microglia response was reduced by N-glycosylation inhibitor tunicamycine while coimmunoprecipitation experiments revealed galectin-3 binding to IGF-receptor 1 (R1), thus suggesting that interaction of galectin-3 with the N-linked glycans of receptors for growth factors is involved in IGF-R1 signaling.	n-linked glycans	260-276	insulin-like growth factor 1	Mus musculus	14-19
22836271-7	2012	Moreover, the IGF-1-mediated mitogenic microglia response was reduced by N-glycosylation inhibitor tunicamycine while coimmunoprecipitation experiments revealed galectin-3 binding to IGF-receptor 1 (R1), thus suggesting that interaction of galectin-3 with the N-linked glycans of receptors for growth factors is involved in IGF-R1 signaling.	n-linked glycans	260-276	lectin, galactose binding, soluble 3	Mus musculus	161-171
22891160-8	2012	Further improvement of V3 immunogenicity is attainable by forming immune complexes with gp120 mutants lacking site-specific N-linked glycans.	n-linked glycans	124-140	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	88-93
22443713-5	2012	The structural model of AtDIR6 was supported experimentally by confirmation of a predicted disulfide bridge and by the characterization of two N-linked glycans at the solvent-exposed protein surface.	n-linked glycans	143-159	Disease resistance-responsive (dirigent-like protein) family protein	Arabidopsis thaliana	24-30
22505413-3	2012	Human p19 and p40 subunits were cloned and coexpressed in N-acetylglucosaminyltransferase I-negative 293S cells, which produce high-mannose-type glycosylated proteins in order to diminish the heterogeneity of modified N-linked glycans.	n-linked glycans	218-234	interleukin 23 subunit alpha	Homo sapiens	6-9
22505413-3	2012	Human p19 and p40 subunits were cloned and coexpressed in N-acetylglucosaminyltransferase I-negative 293S cells, which produce high-mannose-type glycosylated proteins in order to diminish the heterogeneity of modified N-linked glycans.	n-linked glycans	218-234	interleukin 9	Homo sapiens	14-17
22267483-6	2012	Binding studies using purified proteins confirmed that VWF could directly interact with both galectins, predominantly via its N-linked glycans.	n-linked glycans	126-142	Von Willebrand factor	Mus musculus	55-58
22645128-2	2012	N-Linked glycans, which constitute almost half of the molecular mass of the external Env domains, produce considerable structural heterogeneity and are a major impediment to crystallization studies.	n-linked glycans	0-16	endogenous retrovirus group K member 20	Homo sapiens	85-88
22584580-1	2012	Porcine pancreatic alpha-amylase (PPA) binds to N-linked glycans of glycoproteins (Matsushita, H., Takenaka, M., and Ogawa, H. (2002) J. Biol Chem., 277, 4680-4686).	n-linked glycans	48-64	amylase alpha 2A	Homo sapiens	8-32
22628288-1	2012	The human immunodeficiency virus type-1 (HIV-1) is able to shield immunogenic peptide epitopes on its envelope spike (a trimer of two glycoproteins, gp120 and gp41) by presenting numerous host-derived N-linked glycans.	n-linked glycans	201-217	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	149-154
22551306-9	2012	Moreover, PTx is able to activate signaling by binding either N-linked or O-linked glycan-modified receptors as the TCR displays N-linked glycans while CD8zeta displays O-linked glycans.	n-linked glycans	129-145	T cell receptor beta variable 20/OR9-2 (non-functional)	Homo sapiens	116-119
22531441-1	2012	The presence or absence of core fucose in the Fc region N-linked glycans of antibodies affects their binding affinity toward FcgammaRIIIa as well as their antibody-dependent cell-mediated cytotoxicity (ADCC) activity.	n-linked glycans	56-72	Fc gamma receptor IIIa	Homo sapiens	125-137
21932778-9	2011	In summary, we have found that the potential N-glycosylation sites in glypican-1 are invariably occupied and that the N-linked glycans on glypican-1 affect protein expression and heparan sulfate substitution but that correct folding can be obtained in the absence of N-linked glycans.	n-linked glycans	118-134	glypican 1	Homo sapiens	138-148
22792360-4	2012	In this study, we evaluated the effect of modifying N-linked glycans on recombinant human TPP1 on its pharmacokinetic properties after administration via tail vein injection to a mouse model of LINCL.	n-linked glycans	52-68	tripeptidyl peptidase 1	Homo sapiens	90-94
22191536-0	2012	Analysis of folate binding protein N-linked glycans by mass spectrometry.	n-linked glycans	35-51	folate receptor alpha	Homo sapiens	12-34
22191536-8	2012	It was found that FBP from human milk contains putative structures that have composition consistent with high-mannose (Hex(5-6)HexNAc(2)) as well as hybrid and complex N-linked glycans (NeuAc(0-1)Fuc(0-3)Hex(3-6)HexNAc(3-5)).	n-linked glycans	168-184	folate receptor alpha	Homo sapiens	18-21
22191536-9	2012	The FBP from bovine milk contains putative structures corresponding to high-mannose (Hex(4-9)HexNAc(2)) as well as hybrid and complex N-linked glycans (Hex(3-6)HexNAc(3-6)), but these glycans mostly do not contain fucose and sialic acid.	n-linked glycans	134-150	folate receptor alpha	Bos taurus	4-7
22438913-10	2012	In particular, mass spectrometry showed that IGF1R had N-linked glycans at N913 in three figitumumab-sensitive cell lines.	n-linked glycans	55-71	insulin-like growth factor I receptor	Mus musculus	45-50
22093069-4	2011	EF2863 hydrolyzes the glycosidic bond between two N-acetylglucosamines (GlcNAc) in N-linked glycans of the high-mannose and hybrid type, releasing the glycan and leaving one GlcNAc attached to the protein.	n-linked glycans	83-99	chitinase	Enterococcus faecalis V583	0-6
21932778-0	2011	The structural role of N-linked glycans on human glypican-1.	n-linked glycans	23-39	glypican 1	Homo sapiens	49-59
21932778-9	2011	In summary, we have found that the potential N-glycosylation sites in glypican-1 are invariably occupied and that the N-linked glycans on glypican-1 affect protein expression and heparan sulfate substitution but that correct folding can be obtained in the absence of N-linked glycans.	n-linked glycans	267-283	glypican 1	Homo sapiens	70-80
21932778-9	2011	In summary, we have found that the potential N-glycosylation sites in glypican-1 are invariably occupied and that the N-linked glycans on glypican-1 affect protein expression and heparan sulfate substitution but that correct folding can be obtained in the absence of N-linked glycans.	n-linked glycans	267-283	glypican 1	Homo sapiens	138-148
21880749-5	2011	We show here that galectin-1 directly binds to HIV-1 in a beta-galactoside-dependent fashion through recognition of clusters of N-linked glycans on the viral envelope gp120.	n-linked glycans	128-144	galectin 1	Homo sapiens	18-28
21957147-4	2011	The interaction of DCs with HIV-1 involves C-type lectin receptors, such as DC-specific ICAM-3-grabbing nonintegrin, which bind to the envelope glycoprotein complex (Env), which is decorated heavily with N-linked glycans.	n-linked glycans	204-220	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	166-169
21880749-5	2011	We show here that galectin-1 directly binds to HIV-1 in a beta-galactoside-dependent fashion through recognition of clusters of N-linked glycans on the viral envelope gp120.	n-linked glycans	128-144	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	167-172
21697506-5	2011	Partial redistribution of the modified ERManI was observed along with an accelerated rate at which N-linked glycans of misfolded alpha1-antitrypsin variant NHK were trimmed.	n-linked glycans	99-115	serpin family A member 1	Homo sapiens	129-147
21203834-1	2011	We investigated interaction of GM3 with N-acetylglucosamine (GlcNAc) termini of N-linked glycans of epidermal growth factor receptor (EGFR), as the underlying mechanism for inhibitory effect of GM3 on EGFR activation, using ldlD cells transfected with EGFR gene.	n-linked glycans	80-96	Epidermal growth factor receptor	Drosophila melanogaster	100-132
21203834-1	2011	We investigated interaction of GM3 with N-acetylglucosamine (GlcNAc) termini of N-linked glycans of epidermal growth factor receptor (EGFR), as the underlying mechanism for inhibitory effect of GM3 on EGFR activation, using ldlD cells transfected with EGFR gene.	n-linked glycans	80-96	Epidermal growth factor receptor	Drosophila melanogaster	134-138
21715597-0	2011	Removal of two high-mannose N-linked glycans on gp120 renders human immunodeficiency virus 1 largely resistant to the carbohydrate-binding agent griffithsin.	n-linked glycans	28-44	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	48-53
21220208-1	2011	Human CMP-N-acetylneuraminic acid (NeuAc) synthase (hCSS) and alpha2,6-sialyltransferase (hST) participate in the sialylation of N-linked glycans in mammalian cells.	n-linked glycans	129-145	cytidine monophosphate N-acetylneuraminic acid synthetase	Homo sapiens	6-50
21217149-1	2011	Cytoplasmic alpha-mannosidase (Man2C1) has been implicated in non-lysosomal catabolism of free oligosaccharides derived from N-linked glycans accumulated in the cytosol.	n-linked glycans	125-141	mannosidase alpha class 2C member 1	Homo sapiens	31-37
21689651-3	2011	TMEM114 and TMEM235 differed from claudins in terms of localisation in polarised epithelial cells and by the presence of N-linked glycans.	n-linked glycans	121-137	transmembrane protein 114	Xenopus tropicalis	0-7
21220208-1	2011	Human CMP-N-acetylneuraminic acid (NeuAc) synthase (hCSS) and alpha2,6-sialyltransferase (hST) participate in the sialylation of N-linked glycans in mammalian cells.	n-linked glycans	129-145	sulfotransferase family 2A member 1	Homo sapiens	90-93
21220208-2	2011	hCSS synthesizes CMP-NeuAc, which hST uses as a donor substrate to transfer NeuAc to the terminal position of N-linked glycans.	n-linked glycans	110-126	sulfotransferase family 2A member 1	Homo sapiens	34-37
21220208-9	2011	Here, we demonstrate that the in vitro sialylation of N-linked glycans on mammalian proteins can be achieved using plant cell extracts stably expressing hCSS and hST, providing proof-of-principle that a sialylated human therapeutic protein can be produced in plants.	n-linked glycans	54-70	sulfotransferase family 2A member 1	Homo sapiens	162-165
21173156-4	2011	ST6Gal-I adds an alpha2,6-linked sialic acid to the terminal galactose of N-linked glycans, and this modification blocks galectin binding to beta-galactosides.	n-linked glycans	74-90	ST6 beta-galactoside alpha-2,6-sialyltransferase 1	Homo sapiens	0-8
21104290-4	2011	The present review addresses molecular aspects related to E-cadherin N-glycosylation and evidence is presented showing that the modification of N-linked glycans on E-cadherin can affect the adhesive function of this adhesion molecule.	n-linked glycans	144-160	cadherin 1	Homo sapiens	58-68
21104290-4	2011	The present review addresses molecular aspects related to E-cadherin N-glycosylation and evidence is presented showing that the modification of N-linked glycans on E-cadherin can affect the adhesive function of this adhesion molecule.	n-linked glycans	144-160	cadherin 1	Homo sapiens	164-174
21030537-3	2011	In this study, a detailed structure analysis of the N-linked glycans from total glycoproteins from the SKOV3 ovarian carcinoma cell line and from a recombinantly expressed secretory glycoprotein, erythropoietin (EPO), produced from the same cells has been performed using high-performance anion exchange chromatography with pulsed amperometric detection and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.	n-linked glycans	52-68	erythropoietin	Homo sapiens	196-210
21030537-3	2011	In this study, a detailed structure analysis of the N-linked glycans from total glycoproteins from the SKOV3 ovarian carcinoma cell line and from a recombinantly expressed secretory glycoprotein, erythropoietin (EPO), produced from the same cells has been performed using high-performance anion exchange chromatography with pulsed amperometric detection and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.	n-linked glycans	52-68	erythropoietin	Homo sapiens	212-215
21044954-2	2011	In this study, the role of N-linked glycans in modulating APC endothelial cytoprotective signaling via endothelial cell protein C receptor/protease-activated receptor 1 (PAR1) was investigated.	n-linked glycans	27-43	coagulation factor II thrombin receptor	Homo sapiens	170-174
21044954-3	2011	Enzymatic digestion of APC N-linked glycans (PNG-APC) decreased the APC concentration required to achieve half-maximal inhibition of thrombin-induced endothelial cell barrier permeability by 6-fold.	n-linked glycans	27-43	coagulation factor II, thrombin	Homo sapiens	133-141
21042299-7	2011	However, N-linked glycans of human ZP1, ZP3 and ZP4 have important roles in the induction of the AR.	n-linked glycans	9-25	zona pellucida glycoprotein 1	Homo sapiens	35-38
21042299-7	2011	However, N-linked glycans of human ZP1, ZP3 and ZP4 have important roles in the induction of the AR.	n-linked glycans	9-25	zona pellucida glycoprotein 4	Homo sapiens	48-51
20709295-3	2010	Mannose-binding lectin (MBL) recognized N-linked glycans on the structural proteins of WNV and Dengue virus (DENV), resulting in neutralization through a C3- and C4-dependent mechanism that utilized both the canonical and bypass lectin activation pathways.	n-linked glycans	40-56	mannose binding lectin 2	Homo sapiens	0-22
21179548-7	2010	Like its parent protein, GRFN-1 bound viral glycoproteins gp41 and gp120 via the N-linked glycans on their surface.	n-linked glycans	81-97	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	67-72
21218342-7	2011	Biochemical and mass spectrometry analyses in combination with the generation of bovine clusterin subunit-specific antibodies enabled us to demonstrate that it was beta-subunits of clusterin possessing N-linked glycans of complex structure that exhibited differential abundance in response to BSE infection.	n-linked glycans	202-218	clusterin	Bos taurus	181-190
20709295-3	2010	Mannose-binding lectin (MBL) recognized N-linked glycans on the structural proteins of WNV and Dengue virus (DENV), resulting in neutralization through a C3- and C4-dependent mechanism that utilized both the canonical and bypass lectin activation pathways.	n-linked glycans	40-56	mannose binding lectin 2	Homo sapiens	24-27
20709295-6	2010	Experiments in mice showed an MBL-dependent accelerated intravascular clearance of DENV or a WNV mutant with two N-linked glycans on its E protein, but not with wild-type WNV.	n-linked glycans	113-129	mannose-binding lectin (protein C) 2	Mus musculus	30-33
20418283-1	2010	We examined the role that N-linked glycans play in the synthesis and expression of von Willebrand Factor (VWF).	n-linked glycans	26-42	von Willebrand factor	Homo sapiens	83-104
20418283-1	2010	We examined the role that N-linked glycans play in the synthesis and expression of von Willebrand Factor (VWF).	n-linked glycans	26-42	von Willebrand factor	Homo sapiens	106-109
20418283-2	2010	Blocking the addition of N-linked glycans (NLGs) or inhibiting initial glycan processing prevented secretion of VWF.	n-linked glycans	25-41	von Willebrand factor	Homo sapiens	112-115
20418283-9	2010	These data provide further evidence of the critical role that individual N-linked glycans play in determining VWF synthesis and expression.	n-linked glycans	73-89	von Willebrand factor	Homo sapiens	110-113
20210927-2	2010	Expression of ABH antigens on N-linked glycans of VWF protects plasma VWF from proteolysis and clearance.	n-linked glycans	30-46	alkB homolog 1, histone H2A dioxygenase	Homo sapiens	14-17
20379804-3	2010	The terminal sialic acid in the N-linked glycans of FVIII is required for maximal circulatory half life.	n-linked glycans	32-48	coagulation factor VIII	Homo sapiens	52-57
20210927-2	2010	Expression of ABH antigens on N-linked glycans of VWF protects plasma VWF from proteolysis and clearance.	n-linked glycans	30-46	von Willebrand factor	Homo sapiens	50-53
20210927-2	2010	Expression of ABH antigens on N-linked glycans of VWF protects plasma VWF from proteolysis and clearance.	n-linked glycans	30-46	von Willebrand factor	Homo sapiens	70-73
19681908-7	2009	In addition, interleukin-6 production by human dendritic cells was enhanced by C. jejuni lacking N-linked glycans compared with wild-type bacteria.	n-linked glycans	97-113	interleukin 6	Homo sapiens	13-26
20479940-1	2010	BACKGROUND: Peptide:N-glycanase (PNGase) is an enzyme which releases N-linked glycans from glycopeptides/glycoproteins.	n-linked glycans	69-85	PNGase-like	Drosophila melanogaster	12-31
20479940-1	2010	BACKGROUND: Peptide:N-glycanase (PNGase) is an enzyme which releases N-linked glycans from glycopeptides/glycoproteins.	n-linked glycans	69-85	PNGase-like	Drosophila melanogaster	33-39
20306342-5	2010	Interestingly, the lectin showed high affinity for glycans which are part of ovarian cancer marker CA125, a high molecular weight mucin containing high mannose and complex bisecting type N-linked glycans as well core 1 and 2 type O-glycans.	n-linked glycans	187-203	LOC100508689	Homo sapiens	130-135
19884343-1	2010	Alpha-mannosidosis is caused by the genetic defect of the lysosomal alpha-d-mannosidase (LAMAN), which is involved in the breakdown of free alpha-linked mannose-containing oligosaccharides originating from glycoproteins with N-linked glycans, and thus manifests itself in an extensive storage of mannose-containing oligosaccharides.	n-linked glycans	225-241	mannosidase 2, alpha B1	Mus musculus	89-94
19920089-1	2010	Design of an envelope glycoprotein (Env)-based vaccine against human immunodeficiency virus type-1 (HIV-1) is complicated by the large number of N-linked glycans that coat the protein and serve as a barrier to antibody-mediated neutralization.	n-linked glycans	145-161	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	13-34
19920089-1	2010	Design of an envelope glycoprotein (Env)-based vaccine against human immunodeficiency virus type-1 (HIV-1) is complicated by the large number of N-linked glycans that coat the protein and serve as a barrier to antibody-mediated neutralization.	n-linked glycans	145-161	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	36-39
19551866-8	2010	N-linked glycans of serum haptoglobin from colon cancer patients vs. healthy subjects were released by N-glycanase, fluorescence-labeled, and subjected to normal-phase high performance liquid chromatography (NP-HPLC).	n-linked glycans	0-16	haptoglobin	Homo sapiens	26-37
19542522-0	2009	A novel role for Gtb1p in glucose trimming of N-linked glycans.	n-linked glycans	46-62	Gtb1p	Saccharomyces cerevisiae S288C	17-22
19542522-2	2009	It trims the middle and innermost glucose residues (Glc2 and Glc1) from N-linked glycans.	n-linked glycans	72-88	GTPase-activating protein IRA1	Saccharomyces cerevisiae S288C	61-65
19726492-6	2009	N-Linked glycans, released from plasma proteins, were separated using hydrophilic interaction high-performance liquid chromatography into 16 groups (GP1-GP16) and quantified.	n-linked glycans	0-16	GTP binding protein 1	Homo sapiens	149-157
19683346-9	2009	We demonstrate that GdA selectively recognizes complex-type N-linked glycans on T cell surface glycoproteins, and propose that the galectin-1 glycoprotein receptor CD7 maybe a novel target for GdA on T cells.	n-linked glycans	60-76	progestagen associated endometrial protein	Homo sapiens	20-23
19690161-0	2009	Complex N-linked glycans on Asn-89 of Kaposi sarcoma herpes virus-encoded interleukin-6 mediate optimal function by affecting cytokine protein conformation.	n-linked glycans	8-24	interleukin 6	Homo sapiens	74-87
19903263-5	2009	These findings suggest that CD63 interacts with CXCR4 through the N-linked glycans-portion of the CD63 protein and that the complex induces direction of CXCR4 trafficking to the endosomes/lysosomes, rather than to the plasma membrane.	n-linked glycans	66-82	CD63 molecule	Homo sapiens	28-32
19903263-5	2009	These findings suggest that CD63 interacts with CXCR4 through the N-linked glycans-portion of the CD63 protein and that the complex induces direction of CXCR4 trafficking to the endosomes/lysosomes, rather than to the plasma membrane.	n-linked glycans	66-82	C-X-C motif chemokine receptor 4	Homo sapiens	48-53
19903263-5	2009	These findings suggest that CD63 interacts with CXCR4 through the N-linked glycans-portion of the CD63 protein and that the complex induces direction of CXCR4 trafficking to the endosomes/lysosomes, rather than to the plasma membrane.	n-linked glycans	66-82	CD63 molecule	Homo sapiens	98-102
19903263-5	2009	These findings suggest that CD63 interacts with CXCR4 through the N-linked glycans-portion of the CD63 protein and that the complex induces direction of CXCR4 trafficking to the endosomes/lysosomes, rather than to the plasma membrane.	n-linked glycans	66-82	C-X-C motif chemokine receptor 4	Homo sapiens	153-158
19571171-2	2009	Here, we report the sites at which GlcNAc6ST-1 is modified with N-linked glycans and the effects that each glycan has on enzyme activity, specificity, and localization.	n-linked glycans	64-80	carbohydrate sulfotransferase 2	Homo sapiens	35-46
19595807-5	2009	X-ray analysis has shown that each TLR3-ECD of a dimer binds dsRNA at two sites located at opposite ends of the TLR3 "horseshoe" on the one lateral face that lacks N-linked glycans.	n-linked glycans	164-180	toll like receptor 3	Homo sapiens	35-39
19595807-5	2009	X-ray analysis has shown that each TLR3-ECD of a dimer binds dsRNA at two sites located at opposite ends of the TLR3 "horseshoe" on the one lateral face that lacks N-linked glycans.	n-linked glycans	164-180	toll like receptor 3	Homo sapiens	112-116
19443639-6	2009	Bsg isolated from HL-60 cells bound to E-selectin, and tunicamycin treatment to abolish N-linked glycans from Bsg abrogated this binding.	n-linked glycans	88-104	basigin (Ok blood group)	Homo sapiens	0-3
19284292-3	2009	Distinct from these examples, the beta4-GalNAc modification of N-linked glycans on a selected panel of proteins, such as carbonic anhydrase or glycodelin, was demonstrated recently to require specific protein (sequence) determinants proximal to the glycosylation site that function as cis-regulatory elements.	n-linked glycans	63-79	progestagen associated endometrial protein	Homo sapiens	143-153
19415334-10	2009	Lung RAGE appeared to contain two N-linked glycans.	n-linked glycans	34-50	advanced glycosylation end product-specific receptor	Mus musculus	5-9
19465480-4	2009	Negative ion nano-electrospray ionization mass spectra of the 19A N-linked glycans from HEK 293T Lec36 and swainsonine-treated HEK 293T cells were qualitatively indistinguishable and, as shown by collision-induced dissociation spectra, were dominated by hybrid-type glycosylation.	n-linked glycans	66-82	SLAM family member 7	Homo sapiens	62-65
19443639-6	2009	Bsg isolated from HL-60 cells bound to E-selectin, and tunicamycin treatment to abolish N-linked glycans from Bsg abrogated this binding.	n-linked glycans	88-104	selectin E	Homo sapiens	39-49
19443639-6	2009	Bsg isolated from HL-60 cells bound to E-selectin, and tunicamycin treatment to abolish N-linked glycans from Bsg abrogated this binding.	n-linked glycans	88-104	basigin (Ok blood group)	Homo sapiens	110-113
18778316-1	2009	Plant N-linked glycans differ substantially from their mammalian counterparts, mainly with respect to modifications of the core glycan, which typically contains a beta(1,2)-xylose and an alpha(1,3)-fucose.	n-linked glycans	6-22	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	163-171
19303396-2	2009	We investigated whether NK group 2D (NKG2D) and CD94 can bind to sialylated N-linked glycans, using recombinant glutathione S-transferase-fused extracellular lectin-like domains of NKG2D (rNKG2Dlec) and CD94 (rCD94lec).	n-linked glycans	76-92	killer cell lectin like receptor K1	Homo sapiens	24-35
19303396-2	2009	We investigated whether NK group 2D (NKG2D) and CD94 can bind to sialylated N-linked glycans, using recombinant glutathione S-transferase-fused extracellular lectin-like domains of NKG2D (rNKG2Dlec) and CD94 (rCD94lec).	n-linked glycans	76-92	killer cell lectin like receptor K1	Homo sapiens	37-42
19303396-2	2009	We investigated whether NK group 2D (NKG2D) and CD94 can bind to sialylated N-linked glycans, using recombinant glutathione S-transferase-fused extracellular lectin-like domains of NKG2D (rNKG2Dlec) and CD94 (rCD94lec).	n-linked glycans	76-92	killer cell lectin like receptor D1	Homo sapiens	48-52
19053835-3	2009	Applying a highly sensitive glycomics approach which included matrix-assisted laser-desorption ionization and electrospray ionization ion trap mass spectrometry, we have performed a detailed analysis of the N-linked glycans of CD24.	n-linked glycans	207-223	CD24a antigen	Mus musculus	227-231
18778316-1	2009	Plant N-linked glycans differ substantially from their mammalian counterparts, mainly with respect to modifications of the core glycan, which typically contains a beta(1,2)-xylose and an alpha(1,3)-fucose.	n-linked glycans	6-22	adrenoceptor alpha 1D	Homo sapiens	187-196
18922878-6	2008	Additionally, a panel of mutant viruses lacking either individual or multiple N-linked glycosylation sites was used to demonstrate that N-linked glycans were essential for high-level IFN-alpha/beta induction by the mammalian-cell-derived virus.	n-linked glycans	136-152	interferon alpha 1	Homo sapiens	183-192
18632981-3	2008	To better understand the mechanisms regulating protein biogenesis in the mammalian ER, we determined the fate of five variants of soluble BACE with 4, 3, 2, 1, or 0 N-linked glycans.	n-linked glycans	165-181	beta-secretase 1	Homo sapiens	138-142
18606998-4	2008	Klotho treatment increases cell-surface abundance of the renal epithelial Ca(2+) channel TRPV5 by modifying its N-linked glycans.	n-linked glycans	112-128	klotho	Homo sapiens	0-6
18606998-4	2008	Klotho treatment increases cell-surface abundance of the renal epithelial Ca(2+) channel TRPV5 by modifying its N-linked glycans.	n-linked glycans	112-128	transient receptor potential cation channel subfamily V member 5	Homo sapiens	89-94
18426228-2	2008	The primary assay for characterization and lot release of N-linked glycans on glycoprotein products at Genentech, Inc., is a capillary electrophoresis (CE) based assay, wherein PNGase F-released, APTS-labeled glycans are separated by CE with laser induced fluorescence (LIF) detection.	n-linked glycans	58-74	N-glycanase 1	Homo sapiens	177-183
18434410-5	2008	These yeast proteins, like HIV-1 gp120, contain a large number and high density of N-linked glycans, with glycosidase digestion abrogating 2G12 cross-reactivity.	n-linked glycans	83-99	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	33-38
18381078-9	2008	Here, a fraction of ADAM10 from exosomes was found to contain more processed N-linked glycans than the cellular enzyme.	n-linked glycans	77-93	ADAM metallopeptidase domain 10	Homo sapiens	20-26
18426978-5	2008	GT1 reglucosylated N-linked glycans in the slow-folding stem domain of HA once the nascent chain was released from the ribosome.	n-linked glycans	19-35	beta-1,4-galactosyltransferase 1	Homo sapiens	0-3
18385798-5	2008	Cell surface beta1-6 branched N-oligosaccharides were measured by their specific binding to PHA-L followed by flow cytometry, and the fibronectin receptors bearing beta1-6 GlcNAc branched N-linked glycans were identified.	n-linked glycans	188-204	fibronectin 1	Homo sapiens	134-145
17957771-0	2008	N-linked glycans of the human insulin receptor and their distribution over the crystal structure.	n-linked glycans	0-16	insulin receptor	Homo sapiens	30-46
17983356-7	2008	Endo H (endoglycosidase H) treatment and cell culture with alpha-glucosidase inhibitors demonstrated that N-linked glycans are of the complex mature type in the 170 kDa form and of the high-mannose type in the 130 kDa form.	n-linked glycans	106-122	sucrase-isomaltase	Homo sapiens	59-76
17983356-11	2008	Our findings show that N-linked glycans within Ig and/or FNIII domains regulate Ob-R function, but are not involved in essential interactions with the ligand.	n-linked glycans	23-39	leptin receptor	Homo sapiens	80-84
18854874-1	2008	alpha1,6-fucosyltransferase (FUT8) attaches fucose residues via an alpha1,6 linkage to the innermost N-acetylglucosamine residue of N-linked glycans.	n-linked glycans	132-148	fucosyltransferase 8	Homo sapiens	0-27
17975018-10	2008	These data demonstrate that the N-linked glycans of VWF have a modulatory effect on the interaction with ADAMTS13.	n-linked glycans	32-48	von Willebrand factor	Homo sapiens	52-55
17975018-10	2008	These data demonstrate that the N-linked glycans of VWF have a modulatory effect on the interaction with ADAMTS13.	n-linked glycans	32-48	ADAM metallopeptidase with thrombospondin type 1 motif 13	Homo sapiens	105-113
18322210-9	2008	Hence, N-linked glycans are critical determinants that can profoundly influence CD4 T cell recognition of HIV-1 gp120.	n-linked glycans	7-23	CD4 molecule	Homo sapiens	80-83
18322210-9	2008	Hence, N-linked glycans are critical determinants that can profoundly influence CD4 T cell recognition of HIV-1 gp120.	n-linked glycans	7-23	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	112-117
18854874-1	2008	alpha1,6-fucosyltransferase (FUT8) attaches fucose residues via an alpha1,6 linkage to the innermost N-acetylglucosamine residue of N-linked glycans.	n-linked glycans	132-148	fucosyltransferase 8	Homo sapiens	29-33
17634239-4	2007	Here we show that N-linked glycans in addition to the one at position 295 are important in the formation of the 2G12 epitope in subtype C gp120.	n-linked glycans	18-34	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	138-143
17640971-1	2007	CD52 is composed of a 12 amino acid peptide with N-linked glycans bound to the single potential glycosylation site at position 3, and a glycosylphosphatidylinositol-anchor attached at the C-terminus.	n-linked glycans	49-65	CD52 molecule	Homo sapiens	0-4
17356011-8	2007	Studies with PNGase F and tunicamycin reveal the Slc37a2 protein is posttranslationally modified by addition of N-linked glycans.	n-linked glycans	112-128	solute carrier family 37 (glycerol-3-phosphate transporter), member 2	Mus musculus	49-56
17545692-9	2007	These data show that individual N-linked glycans have unique and important effects on the phospholipase activity and substrate specificity of EL.	n-linked glycans	32-48	lipase G, endothelial type	Homo sapiens	142-144
18062249-12	2007	These results indicated that disruptions of MNN1 and OCH1 eliminated the hypermannosylation of the N-linked glycans, and glycoproteins were glycosylated with a single core type glycan, Man8 GlcNAc2, in the mnn1 och1 mutant.	n-linked glycans	99-115	alpha-1,3-mannosyltransferase MNN1	Saccharomyces cerevisiae S288C	44-48
18062249-12	2007	These results indicated that disruptions of MNN1 and OCH1 eliminated the hypermannosylation of the N-linked glycans, and glycoproteins were glycosylated with a single core type glycan, Man8 GlcNAc2, in the mnn1 och1 mutant.	n-linked glycans	99-115	initiation-specific alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	53-57
17678502-3	2007	A major concern is the presence of beta1,2-xylose and core alpha1,3-fucose residues on complex N-linked glycans, as these N-glycan epitopes are immunogenic in mammals.	n-linked glycans	95-111	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	35-42
17678502-3	2007	A major concern is the presence of beta1,2-xylose and core alpha1,3-fucose residues on complex N-linked glycans, as these N-glycan epitopes are immunogenic in mammals.	n-linked glycans	95-111	adrenoceptor alpha 1D	Homo sapiens	59-67
17082223-0	2007	Two N-linked glycans are required to maintain the transport activity of the bile salt export pump (ABCB11) in MDCK II cells.	n-linked glycans	4-20	ATP binding cassette subfamily B member 11	Canis lupus familiaris	99-105
17481579-4	2007	N-linked glycans with the plant-specific sugars beta(1,2)-xylose and alpha(1,3)-fucose comprised 9.8%.	n-linked glycans	0-16	potassium calcium-activated channel subfamily M regulatory beta subunit 1	Homo sapiens	48-56
17375095-0	2007	Rolling on N-linked glycans: a new way to present L-selectin binding sites.	n-linked glycans	11-27	selectin L	Homo sapiens	50-60
17384119-6	2007	This procedure was used to analyze N-linked glycans released from various mixtures of glycoproteins, such as alpha-1 acid glycoprotein, human transferrin, and bovine fetuin, using MS techniques that included matrix assisted laser desorption ionization-time of flight MS and electrospray ionization with ion cyclotron resonance-Fourier transformation MS.	n-linked glycans	35-51	transferrin	Homo sapiens	142-153
17493577-5	2007	Mass spectrometric analysis of cellular N-linked glycans revealed that depletion of VCP decreases the level of high-mannose glycoproteins, increases the levels of truncated low-mannose glycoproteins and induces changes in the abundance of complex glycans assembled in post-ER compartments.	n-linked glycans	40-56	valosin containing protein	Homo sapiens	84-87
17293352-6	2007	The N-linked glycans of recombinant human GAA (rhAGLU), isolated from the rabbit milk, were released by peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase F. The N-glycan pool was fractionated and purified into individual components by a combination of anion-exchange, normal-phase, and Sambucus nigra agglutinin-affinity chromatography.	n-linked glycans	4-20	alpha glucosidase	Homo sapiens	42-45
17264077-10	2007	Therefore, tollo/toll-8 signaling influences flux through several processing steps that affect the maturation of N-linked glycans.	n-linked glycans	113-129	tollo	Drosophila melanogaster	11-23
17082223-9	2007	In conclusion, at least two N-linked glycans are required for Bsep protein stability, intracellular trafficking, and function in the apical membrane.	n-linked glycans	28-44	ATP binding cassette subfamily B member 11	Rattus norvegicus	62-66
17653303-4	2007	Our results show that N-linked glycans may play a role in proper azurocidin folding and subsequent secretion by insect cells.	n-linked glycans	22-38	azurocidin 1	Homo sapiens	65-75
17212372-5	2007	Purified recombinant nephrin was subjected to peptide-N-glycosidase F (PNGase F) to enzymatically remove all the N-linked glycans.	n-linked glycans	113-129	NPHS1 adhesion molecule, nephrin	Homo sapiens	21-28
17152094-6	2007	On the other hand, in Trf, a glycoprotein with only two glycosylation sites, mainly biantennary complex-type-N-linked glycans are bound.	n-linked glycans	109-125	transferrin	Homo sapiens	22-25
17214553-2	2007	Within its cellular pathway, PrP(C) undergoes several posttranslational modifications, i.e., the attachment of two N-linked glycans and a glycosyl phosphatidyl inositol (GPI) anchor, by which it is linked to the plasma membrane on the exterior cell surface.	n-linked glycans	115-131	major prion protein	Cricetulus griseus	29-32
17244731-10	2007	These results indicate that N-linked glycans on ZP1 play an important role in triggering the AR in Japanese quail.	n-linked glycans	28-44	zona pellucida sperm-binding protein 1	Coturnix japonica	48-51
16888005-0	2006	Activation of murine CD4+ and CD8+ T lymphocytes leads to dramatic remodeling of N-linked glycans.	n-linked glycans	81-97	CD4 antigen	Mus musculus	21-24
17071611-4	2006	There are four N-linked glycans on the CD1d heavy chain, and we mutated them individually to ascertain their importance for the assembly and function of CD1d-beta(2)m heterodimers.	n-linked glycans	15-31	CD1d molecule	Homo sapiens	39-43
17071611-4	2006	There are four N-linked glycans on the CD1d heavy chain, and we mutated them individually to ascertain their importance for the assembly and function of CD1d-beta(2)m heterodimers.	n-linked glycans	15-31	CD1d molecule	Homo sapiens	153-157
17071611-4	2006	There are four N-linked glycans on the CD1d heavy chain, and we mutated them individually to ascertain their importance for the assembly and function of CD1d-beta(2)m heterodimers.	n-linked glycans	15-31	beta-2-microglobulin	Homo sapiens	158-166
16919392-7	2006	We conclude that individual N-linked glycans are required for optimal transport of PLB1 to the cell surface and optimal secretion of both PLB1 and PLB1(GPI-).	n-linked glycans	28-44	lysophospholipase	Saccharomyces cerevisiae S288C	83-87
16919392-7	2006	We conclude that individual N-linked glycans are required for optimal transport of PLB1 to the cell surface and optimal secretion of both PLB1 and PLB1(GPI-).	n-linked glycans	28-44	lysophospholipase	Saccharomyces cerevisiae S288C	138-142
16919392-7	2006	We conclude that individual N-linked glycans are required for optimal transport of PLB1 to the cell surface and optimal secretion of both PLB1 and PLB1(GPI-).	n-linked glycans	28-44	lysophospholipase	Saccharomyces cerevisiae S288C	138-142
17165854-1	2006	N-Linked glycans derived from human and bovine alpha1-acid glycoprotein, as well as chicken egg white albumin, were analyzed by MALDI-TOF mass spectrometry using a novel MALDI matrix consisting of 2,5-dihydroxybenzoic acid (DHB) and aniline.	n-linked glycans	0-16	alpha-1-acid glycoprotein	Bos taurus	47-71
17067392-15	2006	The demonstration that N-linked glycans are essential for mediating mesothlein-MUC16 binding may lead to novel therapeutic targets to control the spread of ovarian carcinoma.	n-linked glycans	23-39	mucin 16, cell surface associated	Homo sapiens	79-84
16919392-2	2006	We demonstrated that removal of N-linked glycans from secreted cryptococcal PLB1 leads to loss of enzyme activity.	n-linked glycans	32-48	lysophospholipase	Saccharomyces cerevisiae S288C	76-80
16920935-2	2006	Its preferred ligand is the sequence Sia alpha2-6Gal that is abundantly expressed on N-linked glycans of B cell glycoproteins, and by binding to CD22 in cis causes CD22 to appear "masked" from binding to synthetic sialoside probes.	n-linked glycans	85-101	CD22 molecule	Homo sapiens	145-149
16920935-2	2006	Its preferred ligand is the sequence Sia alpha2-6Gal that is abundantly expressed on N-linked glycans of B cell glycoproteins, and by binding to CD22 in cis causes CD22 to appear "masked" from binding to synthetic sialoside probes.	n-linked glycans	85-101	CD22 molecule	Homo sapiens	164-168
16335978-2	2005	We have utilized micro-solution isoelectric focusing and affinity chromatography, prior to gel electrophoresis to enable site-specific structural determination of the N-linked glycans in apolipoprotein J with the use of FT-ICR MS.	n-linked glycans	167-183	clusterin	Homo sapiens	187-203
16819971-0	2006	Roles of N-linked glycans in the recognition of microbial lipopeptides and lipoproteins by TLR2.	n-linked glycans	9-25	toll like receptor 2	Homo sapiens	91-95
16819971-8	2006	TLR2(N114A,N199A), TLR2(N114A,N414A) and, to a lesser extent, TLR2(N114A,N442A), in which two N-linked glycans are speculated to be exposed to the concave surface of TLR2 solenoid, not only induce NF-kappaB activation but also are associated with wild-type TLR2 and TLR6.	n-linked glycans	94-110	toll like receptor 2	Homo sapiens	0-4
16819971-8	2006	TLR2(N114A,N199A), TLR2(N114A,N414A) and, to a lesser extent, TLR2(N114A,N442A), in which two N-linked glycans are speculated to be exposed to the concave surface of TLR2 solenoid, not only induce NF-kappaB activation but also are associated with wild-type TLR2 and TLR6.	n-linked glycans	94-110	toll like receptor 2	Homo sapiens	19-23
16819971-8	2006	TLR2(N114A,N199A), TLR2(N114A,N414A) and, to a lesser extent, TLR2(N114A,N442A), in which two N-linked glycans are speculated to be exposed to the concave surface of TLR2 solenoid, not only induce NF-kappaB activation but also are associated with wild-type TLR2 and TLR6.	n-linked glycans	94-110	toll like receptor 2	Homo sapiens	19-23
16819971-8	2006	TLR2(N114A,N199A), TLR2(N114A,N414A) and, to a lesser extent, TLR2(N114A,N442A), in which two N-linked glycans are speculated to be exposed to the concave surface of TLR2 solenoid, not only induce NF-kappaB activation but also are associated with wild-type TLR2 and TLR6.	n-linked glycans	94-110	toll like receptor 2	Homo sapiens	19-23
16819971-8	2006	TLR2(N114A,N199A), TLR2(N114A,N414A) and, to a lesser extent, TLR2(N114A,N442A), in which two N-linked glycans are speculated to be exposed to the concave surface of TLR2 solenoid, not only induce NF-kappaB activation but also are associated with wild-type TLR2 and TLR6.	n-linked glycans	94-110	toll like receptor 2	Homo sapiens	19-23
16819971-8	2006	TLR2(N114A,N199A), TLR2(N114A,N414A) and, to a lesser extent, TLR2(N114A,N442A), in which two N-linked glycans are speculated to be exposed to the concave surface of TLR2 solenoid, not only induce NF-kappaB activation but also are associated with wild-type TLR2 and TLR6.	n-linked glycans	94-110	toll like receptor 6	Homo sapiens	266-270
16819971-9	2006	These results suggest that the glycan at Asn442 and at least two N-linked glycans speculated to be exposed to the concave surface of TLR2 solenoid are involved in the recognition of ligands by TLR2 and/or in formation or maturation of a functional TLR2 receptor complex.	n-linked glycans	65-81	toll like receptor 2	Homo sapiens	133-137
16819971-9	2006	These results suggest that the glycan at Asn442 and at least two N-linked glycans speculated to be exposed to the concave surface of TLR2 solenoid are involved in the recognition of ligands by TLR2 and/or in formation or maturation of a functional TLR2 receptor complex.	n-linked glycans	65-81	toll like receptor 2	Homo sapiens	193-197
16819971-9	2006	These results suggest that the glycan at Asn442 and at least two N-linked glycans speculated to be exposed to the concave surface of TLR2 solenoid are involved in the recognition of ligands by TLR2 and/or in formation or maturation of a functional TLR2 receptor complex.	n-linked glycans	65-81	toll like receptor 2	Homo sapiens	193-197
16484342-5	2006	beta3Gal-T1, -T2, and -T5 could synthesize type 1 chains on N-linked glycans, but only beta3Gal-T5 worked on O-linked glycans.	n-linked glycans	60-76	beta-1,3-galactosyltransferase 1	Homo sapiens	0-11
16291658-2	2006	We further define the nature of the epitope recognized by the 6C10 antibody to be a subset of Thy-1 bearing incompletely sialylated N-linked glycans, and furthermore, we demonstrate that tolerant CD4+ T cells have an increased degree of cell-surface sialylation.	n-linked glycans	132-148	thymus cell antigen 1, theta	Mus musculus	94-99
16414019-3	2006	While there is only little sequence homology to mammalian PrP, PrP-related fish proteins were predicted to be modified with N-linked glycans and a C-terminal glycosylphosphatidylinositol (GPI) anchor.	n-linked glycans	124-140	prion protein	Homo sapiens	63-66
16476981-2	2006	Loss of N-linked glycans and increased net charge of the third variable loop (V3) of the gp120 envelope glycoprotein have been observed to be important steps towards CXCR4 use.	n-linked glycans	8-24	C-X-C motif chemokine receptor 4	Homo sapiens	166-171
16219759-1	2005	N-Linked glycans have been shown to have an important role in the cell biology of a variety of cell surface glycoproteins, including PrP protein.	n-linked glycans	0-16	prion protein	Mus musculus	133-136
16769084-1	2006	The Golgi-resident glycosyltransferase, UDP-N-acetyl-d-glucosamine:alpha-3-d-mannoside beta-1,2-N-acetylglucosaminyltransferase I (GnT I), initiates the conversion of high-mannose oligosaccharides to complex and hybrid structures in the biosynthesis of N-linked glycans.	n-linked glycans	253-269	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	40-129
16769084-1	2006	The Golgi-resident glycosyltransferase, UDP-N-acetyl-d-glucosamine:alpha-3-d-mannoside beta-1,2-N-acetylglucosaminyltransferase I (GnT I), initiates the conversion of high-mannose oligosaccharides to complex and hybrid structures in the biosynthesis of N-linked glycans.	n-linked glycans	253-269	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	131-136
16240719-7	2005	They were MNN9 which encodes protein involved in formation of outer chains of the N-linked glycans of secretory proteins and GWT1, encoding the protein of the endoplasmic reticulum involved in the glycosylphosphatidylinositol biosynthesis.	n-linked glycans	82-98	mannosyltransferase complex subunit MNN9	Saccharomyces cerevisiae S288C	10-14
16014566-2	2005	In COS-7 cells transiently transfected with GPVI, deglycosylation with peptide-N-glycosidase F (PNGase F; specific for complex N-linked glycans) or tunicamycin decreases the molecular weight of GPVI and reduces transfected COS-7 cell binding to both CRP and CVX.	n-linked glycans	127-143	glycoprotein VI platelet	Homo sapiens	44-48
16014566-2	2005	In COS-7 cells transiently transfected with GPVI, deglycosylation with peptide-N-glycosidase F (PNGase F; specific for complex N-linked glycans) or tunicamycin decreases the molecular weight of GPVI and reduces transfected COS-7 cell binding to both CRP and CVX.	n-linked glycans	127-143	glycoprotein VI platelet	Homo sapiens	194-198
16091366-4	2005	Because the chaperone calnexin (CN) associates with N-linked glycans, we examined CN interactions with AChR subunits.	n-linked glycans	52-68	calnexin	Homo sapiens	22-30
16091366-4	2005	Because the chaperone calnexin (CN) associates with N-linked glycans, we examined CN interactions with AChR subunits.	n-linked glycans	52-68	calnexin	Homo sapiens	32-34
16091366-7	2005	Additionally, CN associations with subunits lacking N-linked glycans occurred without subunit aggregation or misfolding.	n-linked glycans	52-68	calnexin	Homo sapiens	14-16
15161941-7	2004	Based on these studies, we propose a model of tyrosinase degradation in which interactions between N-linked glycans and lectin chaperones help to minimize tyrosinase aggregation and also target non-native substrates for retro-translocation and subsequent degradation.	n-linked glycans	99-115	tyrosinase	Homo sapiens	46-56
16039588-1	2005	Nascent and newly synthesized glycoproteins enter the calnexin (Cnx)/calreticulin (Crt) cycle when two out of three glucoses in the core N-linked glycans have been trimmed sequentially by endoplasmic reticulum (ER) glucosidases I (GI) and II (GII).	n-linked glycans	137-153	calnexin	Homo sapiens	54-62
16039588-1	2005	Nascent and newly synthesized glycoproteins enter the calnexin (Cnx)/calreticulin (Crt) cycle when two out of three glucoses in the core N-linked glycans have been trimmed sequentially by endoplasmic reticulum (ER) glucosidases I (GI) and II (GII).	n-linked glycans	137-153	calnexin	Homo sapiens	64-67
16039588-1	2005	Nascent and newly synthesized glycoproteins enter the calnexin (Cnx)/calreticulin (Crt) cycle when two out of three glucoses in the core N-linked glycans have been trimmed sequentially by endoplasmic reticulum (ER) glucosidases I (GI) and II (GII).	n-linked glycans	137-153	calreticulin	Homo sapiens	69-81
15728736-7	2005	However, the transfection of GlcNAc6ST-1 resulted in significant sulfate incorporation into CD44 and generated the 6-sulfo LacNAc/Lewis x epitope on CD44, which was present largely on N-linked glycans.	n-linked glycans	184-200	carbohydrate sulfotransferase 2	Homo sapiens	29-40
15728736-7	2005	However, the transfection of GlcNAc6ST-1 resulted in significant sulfate incorporation into CD44 and generated the 6-sulfo LacNAc/Lewis x epitope on CD44, which was present largely on N-linked glycans.	n-linked glycans	184-200	CD44 molecule (Indian blood group)	Homo sapiens	149-153
15919930-4	2005	Both resistant strains exhibited a variety of mutations eliminating N-linked glycans within gp120.	n-linked glycans	68-84	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	92-97
15604092-0	2005	Analysis of N-linked glycans of porcine zona pellucida glycoprotein ZPA by MALDI-TOF MS: a contribution to understanding zona pellucida structure.	n-linked glycans	12-28	zona pellucida glycoprotein 2	Homo sapiens	68-71
15824084-5	2005	PMN-derived CD44 binding activity is mediated by sialylated, alpha(1,3) fucosylated, N-linked glycans.	n-linked glycans	85-101	CD44 molecule (Indian blood group)	Homo sapiens	12-16
16201406-5	2005	Even though rhLF contains oligomannose- and hybrid-type N-linked glycans next to complex-type glycans, which are the only glycans found on natural hLF, the structures are identical within the experimental error (r.m.s.	n-linked glycans	56-72	HLF transcription factor, PAR bZIP family member	Homo sapiens	13-16
15751107-1	2005	N-Linked glycans from bovine ribonuclease B, chicken ovalbumin, bovine fetuin, porcine thyroglobulin and human alpha(1)-acid glycoprotein were derivatized with 2-aminobenzoic acid by reductive amination and their tandem mass spectra were recorded by negative ion electrospray ionization with a quadrupole time-of-flight mass spectrometer.	n-linked glycans	0-16	ovalbumin (SERPINB14)	Gallus gallus	53-62
15657052-7	2005	Both tissue-derived and recombinant testican-2 carried N-linked glycans.	n-linked glycans	55-71	sparc/osteonectin, cwcv and kazal-like domains proteoglycan 2	Mus musculus	36-46
11960993-10	2002	It has previously been proposed that labeling of the Drosophila neural system by anti-horseradish peroxidase antibodies is a result of the presence of difucosylated N-linked glycans.	n-linked glycans	165-181	Peroxidase	Drosophila melanogaster	98-108
14967486-9	2004	These experiments provide direct evidence that the presence of multiple N-linked glycans is required for the proper folding of the E2 protein in the ER and secretory pathway as well as for formation of its antigenic structure.	n-linked glycans	72-88	ubiquitin conjugating enzyme E2 B	Homo sapiens	131-141
12970565-4	2003	We document that alphaMbeta2 is a lectin that recognizes exposed beta-N-acetylglucosamine residues of N-linked glycans on GPIbalpha.	n-linked glycans	102-118	glycoprotein Ib platelet subunit alpha	Homo sapiens	122-131
12734200-6	2003	CA125 is also N-glycosylated, expressing primarily high mannose and complex bisecting type N-linked glycans.	n-linked glycans	91-107	mucin 16, cell surface associated	Homo sapiens	0-5
12489987-3	2002	Here we investigated the influence of the N-linked glycans g1 and g2 present on CXCR4 for HIV-1 infection.	n-linked glycans	42-58	C-X-C motif chemokine receptor 4	Homo sapiens	80-85
12239218-6	2002	Here we show that CD1d associates in the ER with both calnexin and calreticulin and with the thiol oxidoreductase ERp57 in a manner dependent on glucose trimming of its N-linked glycans.	n-linked glycans	169-185	CD1d molecule	Homo sapiens	18-22
12239218-6	2002	Here we show that CD1d associates in the ER with both calnexin and calreticulin and with the thiol oxidoreductase ERp57 in a manner dependent on glucose trimming of its N-linked glycans.	n-linked glycans	169-185	protein disulfide isomerase family A member 3	Homo sapiens	114-119
14707488-1	2002	The glycoprotein UDP-N-acetylglucosamine: beta-D-mannoside-1,4-N-acetylglucosaminyltransferase-III (GnT-III) catalyzes the addition of N-acetylglucosamine via a beta-1, 4-linkage to the beta-linked mannose of the trimannosyl core of N-linked glycans.	n-linked glycans	233-249	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Homo sapiens	4-98
14707488-1	2002	The glycoprotein UDP-N-acetylglucosamine: beta-D-mannoside-1,4-N-acetylglucosaminyltransferase-III (GnT-III) catalyzes the addition of N-acetylglucosamine via a beta-1, 4-linkage to the beta-linked mannose of the trimannosyl core of N-linked glycans.	n-linked glycans	233-249	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Homo sapiens	100-107
15056662-0	2004	Major histocompatibility complex class I molecules expressed with monoglucosylated N-linked glycans bind calreticulin independently of their assembly status.	n-linked glycans	83-99	calreticulin	Homo sapiens	105-117
15056662-4	2004	In vitro analysis of the assembly process has been limited by the specificity of calreticulin for monoglucosylated N-linked glycans, which are transient biosynthetic intermediates.	n-linked glycans	115-131	calreticulin	Homo sapiens	81-93
12952521-0	2003	Processing of N-linked glycans during endoplasmic-reticulum-associated degradation of a short-lived variant of ribophorin I.	n-linked glycans	14-30	ribophorin I	Homo sapiens	111-123
12904308-6	2003	However, the ZPA N-linked glycans were composed of acidic-complex and high-mannose oligosaccharides, ZPX had only high-mannose oligosaccharides, and ZPB lacked N-linked oligosaccharides.	n-linked glycans	17-33	zzona pellucida glycoprotein 2 L homeolog	Xenopus laevis	13-16
14623122-1	2003	UDP-N-acetylglucosamine:alpha(1,6)-D-mannoside beta(1,6)-N-acetylglucosaminyltransferase (GnT-V, Mgat5) functions in the biosynthesis of N-linked glycans and is transcriptionally upregulated by oncogene signaling.	n-linked glycans	137-153	glucosaminyl (N-acetyl) transferase 1	Homo sapiens	47-88
14623122-1	2003	UDP-N-acetylglucosamine:alpha(1,6)-D-mannoside beta(1,6)-N-acetylglucosaminyltransferase (GnT-V, Mgat5) functions in the biosynthesis of N-linked glycans and is transcriptionally upregulated by oncogene signaling.	n-linked glycans	137-153	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	90-95
14623122-1	2003	UDP-N-acetylglucosamine:alpha(1,6)-D-mannoside beta(1,6)-N-acetylglucosaminyltransferase (GnT-V, Mgat5) functions in the biosynthesis of N-linked glycans and is transcriptionally upregulated by oncogene signaling.	n-linked glycans	137-153	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	97-102
12270713-2	2002	Similar to its membrane-bound homolog calnexin (CNX), it is a lectin that promotes the folding of proteins carrying N-linked glycans.	n-linked glycans	116-132	calnexin	Homo sapiens	48-51
12042249-2	2002	N-Linked glycans were released with peptide-N-glycosidase F (PNGase F) within gel from SDS-PAGE-isolated soluble and glycosylphosphatidylinositol (GPI)-anchored human CD59 expressed in CHO cells.	n-linked glycans	0-16	CD59 molecule (CD59 blood group)	Homo sapiens	167-171
11952786-6	2002	Trimming of the N-linked glycans gave rise to glycosylated Ac45-forms of approximately 61 and approximately 63 kDa that are cleaved to a C-terminal fragment of 42-44 kDa (the deglycosylated form is approximately 23 kDa), and a previously not detected approximately 22-kDa N-terminal cleavage fragment (the deglycosylated form is approximately 20 kDa).	n-linked glycans	16-32	ATPase H+ transporting accessory protein 1	Homo sapiens	59-63
11590221-2	2001	We show that human macrophages synthesize PAF-AH as a premedial Golgi precursor containing high mannose N-linked glycans.	n-linked glycans	104-120	phospholipase A2 group VII	Homo sapiens	42-48
11901167-5	2002	The strongly reduced cellulose content of knf mutants indicates that N-linked glycans are required for cellulose biosynthesis.	n-linked glycans	69-85	glucosidase 1	Arabidopsis thaliana	42-45
11834538-1	2002	To investigate whether the effect of ABO blood group on plasma von Willebrand factor (vWF) levels is mediated by the ABH antigenic determinants carried on N-linked glycans of vWF, we studied 158 group A and group O healthy volunteers.	n-linked glycans	155-171	von Willebrand factor	Homo sapiens	175-178
11754484-1	2002	The Saccharomyces cerevisiae OCH1 gene encodes an alpha-1,6-mannosyltransferase that initiates the polymannose outer chain elongation of N-linked glycans.	n-linked glycans	137-153	initiation-specific alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	29-33
11754484-1	2002	The Saccharomyces cerevisiae OCH1 gene encodes an alpha-1,6-mannosyltransferase that initiates the polymannose outer chain elongation of N-linked glycans.	n-linked glycans	137-153	alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	50-79
11583570-1	2001	The N-linked glycans on transferrin and alpha(1)-antitrypsin from patients with congenital disorders of glycosylation type I have increased fucosylation and branching relative to normal controls.	n-linked glycans	4-20	transferrin	Homo sapiens	24-35
11868814-7	2002	Removal of the N-linked glycans from PH-20 with N-glycosidase F shifted the molecular weight from 64 kd to approximately 54 kd, its deduced molecular weight based on sequence analysis, suggesting that most if not all, of the potential N-glycosylation sites are linked to oligosaccharides.	n-linked glycans	15-31	sperm adhesion molecule 1	Homo sapiens	37-42
11672902-2	2001	DNA encoding HIV-1 env is a poorly efficient B-cell immunogen and one probable explanation is that the numerous gp120 N-linked glycans gp120 may interfere with B-cell epitope presentation.	n-linked glycans	118-134	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	19-22
11672902-2	2001	DNA encoding HIV-1 env is a poorly efficient B-cell immunogen and one probable explanation is that the numerous gp120 N-linked glycans gp120 may interfere with B-cell epitope presentation.	n-linked glycans	118-134	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	112-117
11672902-2	2001	DNA encoding HIV-1 env is a poorly efficient B-cell immunogen and one probable explanation is that the numerous gp120 N-linked glycans gp120 may interfere with B-cell epitope presentation.	n-linked glycans	118-134	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	135-140
11676606-8	2001	Together, these results indicate that the presence of varied types of N-linked glycans on asparagine 240 of CD154 does not play a significant role in the CD40-CD154 interactions.	n-linked glycans	70-86	CD40 ligand	Homo sapiens	108-113
11590221-3	2001	Secreted PAF-AH possesses a molecular mass of approximately 55 kDa and contains mature N-linked glycans.	n-linked glycans	87-103	phospholipase A2 group VII	Homo sapiens	9-15
11467936-2	2001	A key enzyme in regulating the maturation of N-linked glycans is UDP-N-acetylglucosamine:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I (GlcNAc-TI, EC 2.4.1.101).	n-linked glycans	45-61	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Oryctolagus cuniculus	65-151
11501752-12	2001	CONCLUSIONS: (1) The highest elevation of GnT-III and the close relationship between the WGA binding of BCa Fn with the pathological stage and grade of BCa indicate that the increase of bisecting GlcNAc in N-linked glycans contributes more to the malignant behavior of BCa than the increase of GnT-IV, GnT-V, and the antennary number.	n-linked glycans	206-222	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Homo sapiens	42-49
11501752-12	2001	CONCLUSIONS: (1) The highest elevation of GnT-III and the close relationship between the WGA binding of BCa Fn with the pathological stage and grade of BCa indicate that the increase of bisecting GlcNAc in N-linked glycans contributes more to the malignant behavior of BCa than the increase of GnT-IV, GnT-V, and the antennary number.	n-linked glycans	206-222	fibronectin 1	Homo sapiens	108-110
11467936-2	2001	A key enzyme in regulating the maturation of N-linked glycans is UDP-N-acetylglucosamine:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I (GlcNAc-TI, EC 2.4.1.101).	n-linked glycans	45-61	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Oryctolagus cuniculus	153-162
11485624-2	2001	Here, we determined whether N-linked glycans of other gp120 domains were also involved in protection of V3 neutralization epitopes.	n-linked glycans	28-44	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	54-59
11485624-4	2001	gp120 from both mutated viral clones had higher electrophoretic mobilities than gp120 from wild-type virus, confirming loss of N-linked glycans.	n-linked glycans	127-143	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	0-5
11485624-9	2001	In conclusion, one or more N-linked glycans of gp120 V1 is engaged in protection of the V3 region from potential neutralizing antibodies, and this effect is dependent on the oligomeric organization of gp120/gp41.	n-linked glycans	27-43	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	47-52
11485624-9	2001	In conclusion, one or more N-linked glycans of gp120 V1 is engaged in protection of the V3 region from potential neutralizing antibodies, and this effect is dependent on the oligomeric organization of gp120/gp41.	n-linked glycans	27-43	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	201-206
11677785-7	2001	Profiles of the N-linked glycans of the individual isoforms of alpha 1-antitrypsin were obtained by MALDI-TOF.	n-linked glycans	16-32	serpin family A member 1	Homo sapiens	63-82
11376005-7	2001	Mapping studies using CD2 point mutation, deletion, and chimeric molecules suggest that conformational change in the CD2 ectodomain participates in inducible raft association and excludes the membrane-proximal N-linked glycans, the transmembrane segment, and the CD2 cytoplasmic region (residues 8-117) as necessary for translocation.	n-linked glycans	210-226	CD2 molecule	Homo sapiens	117-120
11376005-7	2001	Mapping studies using CD2 point mutation, deletion, and chimeric molecules suggest that conformational change in the CD2 ectodomain participates in inducible raft association and excludes the membrane-proximal N-linked glycans, the transmembrane segment, and the CD2 cytoplasmic region (residues 8-117) as necessary for translocation.	n-linked glycans	210-226	CD2 molecule	Homo sapiens	117-120
11256998-4	2001	We demonstrate a major difference in the galactosylation of N-linked glycans isolated from neuronal (i.e. brain-derived) SIRP alpha as compared to myeloid (i.e. spleen-derived) SIRP alpha, with neuronal SIRP alpha almost completely lacking galactose.	n-linked glycans	60-76	signal regulatory protein alpha	Homo sapiens	121-131
11298743-4	2001	We first targeted a cluster of three N-linked glycans in the LHR (N295, N303, N317) in a region corresponding to the primary TSHR cleavage site, which has only one N-linked glycan.	n-linked glycans	37-53	thyroid stimulating hormone receptor	Homo sapiens	125-129
11287403-1	2001	The alpha1,6 fucosyltransferase (alpha1,6 FucT) catalyzes the transfer of a fucose from GDP-fucose to the innermost GlcNAc residue of N-linked glycans via an alpha1,6 linkage.	n-linked glycans	134-150	fucosyltransferase 8	Mus musculus	4-31
11315257-8	2001	In contrast, GnT-V-AS/7721 cells showed reduction of both GnT-V activity and content of the beta 1,6 branch in N-linked glycans, elevation of cell attachment to Fn or Ln, and decline of cell migration and invasion through matrigel.	n-linked glycans	111-127	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	13-18
11315257-11	2001	The product of GnT-V, the beta 1,6 GlcNAc branch in N-linked glycans, is a structural factor of adhesion inhibition and invasion promotion.	n-linked glycans	52-68	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	15-20
11287403-1	2001	The alpha1,6 fucosyltransferase (alpha1,6 FucT) catalyzes the transfer of a fucose from GDP-fucose to the innermost GlcNAc residue of N-linked glycans via an alpha1,6 linkage.	n-linked glycans	134-150	fucosyltransferase 8	Mus musculus	33-46
11181557-0	2001	Loss of N-linked glycans in the V3-loop region of gp120 is correlated to an enhanced infectivity of HIV-1.	n-linked glycans	8-24	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	50-55
11161453-4	2001	Immunoblotting studies revealed that the PrP(C) glycoforms and the composition of the N-linked glycans on PrP(C) in human PBMC are different from those of the brain or the neuroblastoma cells.	n-linked glycans	86-102	prion protein	Homo sapiens	106-112
11159917-2	2000	The HSV-1 glycoprotein gC-1 is highly glycosylated and contains not only N-linked glycans but also a large number of O-linked glycans, some of which are clustered into two pronase-resistant arrays in the vicinity of the HSV-1 receptor-binding domain of gC-1.	n-linked glycans	73-89	solute carrier family 25 member 22	Homo sapiens	23-27
11095749-3	2000	This L-selectin ligand activity of CD44 requires sialofucosylated N-linked glycans and is sulfation-independent.	n-linked glycans	66-82	selectin L	Homo sapiens	5-15
11095749-3	2000	This L-selectin ligand activity of CD44 requires sialofucosylated N-linked glycans and is sulfation-independent.	n-linked glycans	66-82	CD44 molecule (Indian blood group)	Homo sapiens	35-39
11030742-2	2000	To investigate the influence of both the two N-linked glycans, Asn181 and Asn197, and of the GPI anchor attached to Ser230, on the structural, dynamical and electrostatic behavior of PrP, we have undertaken molecular dynamics simulations on the C-terminal region of human prion protein HU:PrP(90-230), with and without the three glycans.	n-linked glycans	45-61	prion protein	Homo sapiens	183-186
10814701-1	2000	UDP-GlcNAc: Manalpha1-6Manbeta-R beta1-6 N-acetylglucosaminyltransferase V (EC 2.4.1.155, GlcNAc-TV) is a Golgi enzyme that substitutes the trimannosyl core in the biosynthetic pathway for complex-type N-linked glycans.	n-linked glycans	202-218	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	41-74
10908805-1	2000	The major cationic peanut (Arachis hypogaea) peroxidase, secreted into the extracellular space, is a glycoprotein with three N-linked glycans (polysaccharides) which are connected to the peptide backbone at Asn-60, Asn-144 and Asn-185.	n-linked glycans	125-141	peroxidase N1-like	Nicotiana tabacum	45-55
10913312-5	2000	Trapping of apo(a) N-linked glycans in their monoglucosylated form, by posttranslational inhibition of ER glucosidase activity with castanospermine (CST), enhanced apo(a)-CNX/CRT interaction and prevented both apo(a) secretion and ERAD.	n-linked glycans	19-35	calnexin	Homo sapiens	171-174
10913312-5	2000	Trapping of apo(a) N-linked glycans in their monoglucosylated form, by posttranslational inhibition of ER glucosidase activity with castanospermine (CST), enhanced apo(a)-CNX/CRT interaction and prevented both apo(a) secretion and ERAD.	n-linked glycans	19-35	calreticulin	Homo sapiens	175-178
10814701-1	2000	UDP-GlcNAc: Manalpha1-6Manbeta-R beta1-6 N-acetylglucosaminyltransferase V (EC 2.4.1.155, GlcNAc-TV) is a Golgi enzyme that substitutes the trimannosyl core in the biosynthetic pathway for complex-type N-linked glycans.	n-linked glycans	202-218	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	90-99
10782293-1	2000	Structures of the N-linked glycans released from porcine kidney diamine oxidase (DAO) were characterized utilizing various analytical techniques, including matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI/TOF-MS), high-performance capillary electrophoresis (HPCE), and high-pH anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD).	n-linked glycans	18-34	amine oxidase copper containing 1	Homo sapiens	64-79
10700233-1	2000	Golgi beta1,6N-acetylglucosaminyltransferase V (MGAT5) is required in the biosynthesis of beta1,6GlcNAc-branched N-linked glycans attached to cell surface and secreted glycoproteins.	n-linked glycans	113-129	mannoside acetylglucosaminyltransferase 5	Mus musculus	6-46
10700233-1	2000	Golgi beta1,6N-acetylglucosaminyltransferase V (MGAT5) is required in the biosynthesis of beta1,6GlcNAc-branched N-linked glycans attached to cell surface and secreted glycoproteins.	n-linked glycans	113-129	mannoside acetylglucosaminyltransferase 5	Mus musculus	48-53
10782293-1	2000	Structures of the N-linked glycans released from porcine kidney diamine oxidase (DAO) were characterized utilizing various analytical techniques, including matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI/TOF-MS), high-performance capillary electrophoresis (HPCE), and high-pH anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD).	n-linked glycans	18-34	amine oxidase copper containing 1	Homo sapiens	81-84
10518544-1	1999	One function of N-linked glycans is to assist in the folding of glycoproteins by mediating interactions of the lectin-like chaperone proteins calnexin and calreticulin with nascent glycoproteins.	n-linked glycans	16-32	calnexin	Homo sapiens	142-150
11114021-8	2000	The technique was applied to the structural determination of N-linked glycans from human secretory IgA and Apo-B 100 from human low-density lipoprotein.	n-linked glycans	61-77	apolipoprotein B	Homo sapiens	107-116
10529240-6	1999	More than 95% of the N-linked glycans attached to both gelatinase B and NGAL were partially sialylated, core-fucosylated biantennary structures with and without outer arm fucose.	n-linked glycans	21-37	lipocalin 2	Homo sapiens	72-76
10514467-14	1999	These data confirm that male genital tract CD52 is distinct from the lymphocyte form by both N-linked glycans and COOH-terminal attached lipid anchor.	n-linked glycans	93-109	CD52 molecule	Homo sapiens	43-47
10617625-7	2000	Its N-linked glycans helped regulate the thermal stability of mMCP-7.	n-linked glycans	4-20	tryptase alpha/beta 1	Mus musculus	62-68
10518544-1	1999	One function of N-linked glycans is to assist in the folding of glycoproteins by mediating interactions of the lectin-like chaperone proteins calnexin and calreticulin with nascent glycoproteins.	n-linked glycans	16-32	calreticulin	Homo sapiens	155-167
10486256-3	1999	Treatment of rats with this unphysiological precursor resulted in an incorporation of N-propanoylneuraminic acid into N-linked glycans of dipeptidyl peptidase IV.	n-linked glycans	118-134	dipeptidylpeptidase 4	Rattus norvegicus	138-161
10548047-0	1999	Structure and function of the N-linked glycans of HBP/CAP37/azurocidin: crystal structure determination and biological characterization of nonglycosylated HBP.	n-linked glycans	30-46	azurocidin 1	Homo sapiens	50-53
10548047-0	1999	Structure and function of the N-linked glycans of HBP/CAP37/azurocidin: crystal structure determination and biological characterization of nonglycosylated HBP.	n-linked glycans	30-46	azurocidin 1	Homo sapiens	54-59
10548047-0	1999	Structure and function of the N-linked glycans of HBP/CAP37/azurocidin: crystal structure determination and biological characterization of nonglycosylated HBP.	n-linked glycans	30-46	azurocidin 1	Homo sapiens	60-70
10548047-0	1999	Structure and function of the N-linked glycans of HBP/CAP37/azurocidin: crystal structure determination and biological characterization of nonglycosylated HBP.	n-linked glycans	30-46	azurocidin 1	Homo sapiens	155-158
10484609-1	1999	The addition and endoplasmic reticulum (ER) glucosidase processing of N-linked glycans is essential for the secretion of rat hepatic lipase (HL).	n-linked glycans	70-86	lipase C, hepatic type	Rattus norvegicus	125-139
10484609-1	1999	The addition and endoplasmic reticulum (ER) glucosidase processing of N-linked glycans is essential for the secretion of rat hepatic lipase (HL).	n-linked glycans	70-86	lipase C, hepatic type	Rattus norvegicus	141-143
10484609-4	1999	Steady-state and pulse-chase labeling experiments established that human HL was synthesized as an ER-associated precursor containing high mannose N-linked glycans.	n-linked glycans	146-162	lipase C, hepatic type	Homo sapiens	73-75
10441510-1	1999	N-Acetylglucosaminyltransferase I (GlcNAcT-I, EC 2.4.1.101) is the enzyme which initiates the formation of complex N-linked glycans in eukaryotes by transforming GlcNAc to the oligo-mannosyl acceptor Man(5)GlcNAc(2)-Asn.	n-linked glycans	115-131	alpha-1,3-mannosyl-glycoprotein beta-1,2-N-acetylglucosaminyltransferase	Arabidopsis thaliana	0-33
10441510-1	1999	N-Acetylglucosaminyltransferase I (GlcNAcT-I, EC 2.4.1.101) is the enzyme which initiates the formation of complex N-linked glycans in eukaryotes by transforming GlcNAc to the oligo-mannosyl acceptor Man(5)GlcNAc(2)-Asn.	n-linked glycans	115-131	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	35-44
10225975-8	1999	A novel glycoprotein ligand of 240 kDa carrying N-linked glycans was isolated from B-cell membranes by an E-selectin immunoadhesin.	n-linked glycans	48-64	selectin E	Homo sapiens	106-116
10350067-1	1999	In the present study we show that the H (0) blood group determinant Fuc alpha1-2Gal beta1-4GlcNAc beta1-R is present on N-linked glycans of soluble human L-selectin recombinantly expressed in baby hamster kidney (BHK) cells.	n-linked glycans	120-136	selectin L	Homo sapiens	154-164
10645146-2	1999	THP is heavily glycosylated by N-linked glycans, which are responsible for most of its properties.	n-linked glycans	31-47	uromodulin	Homo sapiens	0-3
9799111-11	1998	Carbohydrate analysis identified N-linked glycans on CD5 domains 1 and 2, and sialylated O-linked glycans on the linker peptide between domains 1 and 2.	n-linked glycans	33-49	T-cell surface glycoprotein CD5	Cricetulus griseus	53-56
9820138-1	1998	The three flavivirus glycoproteins prM, E and NS1 are formed by post-translational cleavage and are glycosylated by the addition of N-linked glycans.	n-linked glycans	132-148	influenza virus NS1A binding protein	Homo sapiens	46-49
9859110-3	1998	Such tyrosine-based motifs have also been shown to act as basolateral targeting signals, whilst N-linked glycans (as occur on the extracytosolic domain of TGN38) can act as apical targeting signals.	n-linked glycans	96-112	trans-golgi network protein 2	Homo sapiens	155-160
9637923-6	1998	Recently, the thiol oxidoreductase ERp57--also known as GRP58, ERp61, ER60, Q2, HIP-70, and CPT and first misidentified as phospholipase C-alpha--has been shown to bind in conjunction with calnexin or calreticulin to a number of newly synthesized ER glycoproteins when their N-linked glycans are trimmed by glucosidases I and II.	n-linked glycans	275-291	protein disulfide isomerase family A member 3	Homo sapiens	35-40
9497314-3	1998	The type I membrane-protein calnexin and its soluble homologue calreticulin are constituents of this system that recognize monoglucosylated N-linked glycans that are present on unfolded glycoproteins.	n-linked glycans	140-156	calnexin	Homo sapiens	28-36
9555945-4	1998	The data from the combination of FAB spectrometry and linkage analysis show that the N-linked glycans present on recombinant LCAT (rLCAT) were composed primarily of triantennary and tetraantennary structures with and without core fucosylation.	n-linked glycans	85-101	FA complementation group B	Homo sapiens	33-36
9555945-4	1998	The data from the combination of FAB spectrometry and linkage analysis show that the N-linked glycans present on recombinant LCAT (rLCAT) were composed primarily of triantennary and tetraantennary structures with and without core fucosylation.	n-linked glycans	85-101	lecithin-cholesterol acyltransferase	Homo sapiens	125-129
9497314-3	1998	The type I membrane-protein calnexin and its soluble homologue calreticulin are constituents of this system that recognize monoglucosylated N-linked glycans that are present on unfolded glycoproteins.	n-linked glycans	140-156	calreticulin	Homo sapiens	63-75
9357103-1	1997	The N-linked glycans assembled in Pichia pastoris on the recombinant kringle 2 domain of human tissue-type plasminogen activator (r-[K2tPA]) are composed of approx.	n-linked glycans	4-20	plasminogen activator, tissue type	Homo sapiens	95-128
9442118-7	1998	Four distinct oligosaccharide structures were found to effect CD44-mediated HA binding: (a) the terminal alpha2,3-linked sialic acid on N-linked oligosaccharides inhibited binding; (b) the first N-linked N-acetylglucosamine residue enhanced binding; (c) O-linked glycans on N-deglycosylated CD44 enhanced binding; and (d) N-acetylgalactosamine incorporation into non-N-linked glycans augmented HA binding by cell surface CD44.	n-linked glycans	367-383	CD44 antigen	Cricetulus griseus	62-66
9299469-0	1997	NKR-P1A protein, an activating receptor of rat natural killer cells, binds to the chitobiose core of uncompletely glycosylated N-linked glycans, and to linear chitooligomers.	n-linked glycans	127-143	killer cell lectin-like receptor subfamily B, member 1A	Rattus norvegicus	0-7
9383252-7	1997	Its N-terminal and internal sequences, N-linked glycans, and enzymatic activity indicated that this allergen is a seed-specific peroxidase.	n-linked glycans	39-55	peroxidase-like	Triticum aestivum	128-138
9003768-4	1996	When expressed with two N-linked glycans in the presence of micromolar concentrations of deoxynojirimycin, this small soluble protein was found to bind firmly to both calnexin and calreticulin.	n-linked glycans	24-40	calreticulin	Bos taurus	180-192
9147064-1	1997	ST6Gal I (beta-galactoside alpha 2,6-sialyltransferase, SiaT-1, ST6N, EC 2.4.99.1) mediates the attachment of the alpha 2,6-sialyl linkage common on N-linked glycans.	n-linked glycans	149-165	beta galactoside alpha 2,6 sialyltransferase 1	Mus musculus	0-8
9147064-1	1997	ST6Gal I (beta-galactoside alpha 2,6-sialyltransferase, SiaT-1, ST6N, EC 2.4.99.1) mediates the attachment of the alpha 2,6-sialyl linkage common on N-linked glycans.	n-linked glycans	149-165	beta galactoside alpha 2,6 sialyltransferase 1	Mus musculus	56-62
9020131-0	1997	Reglucosylation of N-linked glycans is critical for calnexin assembly with T cell receptor (TCR) alpha proteins but not TCRbeta proteins.	n-linked glycans	19-35	calnexin	Homo sapiens	52-60
9672607-3	1997	In the present report we determined whether fucose units also were linked to the distal GlcNAc via alpha(1-3) or alpha(1-4) linkages in N-linked glycans of gp 120.	n-linked glycans	136-152	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	156-162
9672607-4	1997	[3H]-fucose labelled gp 120 was subjected to endoglycosidase F digestion, releasing diantennary complex type N-linked glycans, but leaving the inner polypeptide-bound carbohydrates, GlcNAc and possibly associated fucose units, intact.	n-linked glycans	109-125	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	21-27
9672607-7	1997	Altogether the results indicated presence of fucose units linked to peripheral GlcNAc of gp 120 N-linked glycans.	n-linked glycans	96-112	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	89-95
9672607-8	1997	We have earlier shown that other peripheral carbohydrate determinants, i.e. beta(1-4)-galactose on N-linked glycans, maintain a correct antigenic conformation of gp 120.	n-linked glycans	99-115	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	76-84
9672607-8	1997	We have earlier shown that other peripheral carbohydrate determinants, i.e. beta(1-4)-galactose on N-linked glycans, maintain a correct antigenic conformation of gp 120.	n-linked glycans	99-115	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	162-168
9672607-9	1997	Using a coupled ELISA system, where changes in antigenic behaviour of a viral glycoprotein were correlated to stepwise elimination of peripheral monosaccharides from N-linked glycans, we found that treatment of gp 120 with a pan-specific alpha-fucosidase as well as an enzyme specific for alpha(1-3)- or alpha(1-4)-linked fucose disclosed a hidden linear epitope situated in the gp 120 C2 region.	n-linked glycans	166-182	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	211-217
9003768-4	1996	When expressed with two N-linked glycans in the presence of micromolar concentrations of deoxynojirimycin, this small soluble protein was found to bind firmly to both calnexin and calreticulin.	n-linked glycans	24-40	calnexin	Bos taurus	167-175
9228058-2	1997	When human soluble FasL (sFasL, containing the extracellular portion) was expressed in human embryo kidney 293 cells, the three N-linked glycans of each FasL monomer were found to be essential for efficient secretion.	n-linked glycans	128-144	Fas ligand	Homo sapiens	19-23
9228058-2	1997	When human soluble FasL (sFasL, containing the extracellular portion) was expressed in human embryo kidney 293 cells, the three N-linked glycans of each FasL monomer were found to be essential for efficient secretion.	n-linked glycans	128-144	Fas ligand	Homo sapiens	26-30
9153399-8	1997	A bend between domains 1 and 2 of ICAM-2 and a tripod-like arrangement of N-linked glycans in the membrane-proximal region of domain 2 may be important for presenting the recognition surface to LFA-1.	n-linked glycans	74-90	integrin subunit alpha L	Homo sapiens	194-199
9013598-3	1997	The mass spectra of the glycopeptides exhibit characteristic clusters of peaks which indicate the N-linked glycans in tACE to be mostly of the biantennary, fucosylated complex type.	n-linked glycans	98-114	ADAM metallopeptidase domain 17	Homo sapiens	118-122
9672607-0	1997	Demonstration of peripheral fucose units in N-linked glycans of human immunodeficiency virus type 1 gp 120: effects on glycoprotein conformation.	n-linked glycans	44-60	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	100-106
8955372-0	1996	Calnexin can interact with N-linked glycans located close to the endoplasmic reticulum membrane.	n-linked glycans	27-43	calnexin	Homo sapiens	0-8
8943049-0	1996	Deglucosylation of N-linked glycans is an important step in the dissociation of calreticulin-class I-TAP complexes.	n-linked glycans	19-35	calreticulin	Mus musculus	80-92
8943049-4	1996	Finally, these studies show that deglucosylation of N-linked glycans is important for dissociation of class I proteins from both calreticulin and TAP and that the vast majority of newly synthesized class I proteins associated with calreticulin are simultaneously assembled with TAP.	n-linked glycans	52-68	calreticulin	Mus musculus	129-141
8910328-1	1996	The Lec4A and Lec4 Chinese hamster ovary glycosylation mutants lack N-linked glycans with GlcNAcbeta(1,6)Manalpha(1,6) branches that are initiated by the transferase termed GlcNAc-TV.	n-linked glycans	68-84	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A	Cricetulus griseus	173-182
8687384-4	1996	Further we show that Bowes t-PA expresses glucuronic acid/sulphate containing N-linked glycans and is recognized by anti-carbohydrate L2/HNK-1 monoclonal antibodies.	n-linked glycans	78-94	chromosome 20 open reading frame 181	Homo sapiens	27-31
8673525-2	1996	The aim of the present study was to explore the possibility to obtain a more broadly neutralizing immune response by immunizing guinea pigs with gp160 depleted of three N-linked glycans in the CD4-binding domain by site-directed mutagenesis.	n-linked glycans	169-185	glutamyl aminopeptidase	Homo sapiens	145-150
8673525-8	1996	These data indicated that elimination of the three N-linked glycans from gp160 resulted in an altered local antigenic conformation but did not uncover hidden neutralization epitopes, broadening the immune response.	n-linked glycans	51-67	glutamyl aminopeptidase	Homo sapiens	73-78
8888624-2	1996	In Arabidopsis seedlings, accumulation of transcripts for BiP was induced not only by inhibition of the N-glycosylation of proteins by tunicamycin but also by inhibition of the processing of N-linked glycans by castanospermine.	n-linked glycans	191-207	Heat shock protein 70 (Hsp 70) family protein	Arabidopsis thaliana	58-61
8673525-0	1996	Influence of N-linked glycans in V4-V5 region of human immunodeficiency virus type 1 glycoprotein gp160 on induction of a virus-neutralizing humoral response.	n-linked glycans	13-29	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	98-103
8687384-2	1996	This study clarified an earlier discrepancy in the literature and confirmed that the major complex N-linked glycans on Bowes t-PA that carry sialic acid as their sole charged group are bi-antennary, core fucosylated, with terminal N-acetylgalactosamine residues.	n-linked glycans	99-115	chromosome 20 open reading frame 181	Homo sapiens	125-129
8560759-0	1996	N-linked glycans in the CD4-binding domain of human immunodeficiency virus type 1 envelope glycoprotein gp160 are essential for the in vivo priming of T cells recognizing an epitope located in their vicinity.	n-linked glycans	0-16	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	104-109
8973529-1	1996	We have constructed a mutated infectious HIV variant lacking the signals for addition of three N-linked glycans situated in the V4, C4 and V5 regions of HIV gp120.	n-linked glycans	95-111	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	157-162
8950359-8	1996	In contrast, only high mannose-type N-linked glycans are present on the PSMA from LNCaP cells.	n-linked glycans	36-52	folate hydrolase 1	Homo sapiens	72-76
8950359-10	1996	N-linked glycans of PSMA derived from in vivo sources were found to be complex type, lacking polylactosamine structures.	n-linked glycans	0-16	folate hydrolase 1	Homo sapiens	20-24
7538125-4	1995	The inefficient folding of hCG-beta lacking both N-linked glycans correlated with the slow formation of the last three disulfide bonds (i.e. disulfides 23-72, 93-100, and 26-110) to form in the hCG-beta-folding pathway.	n-linked glycans	49-65	chorionic gonadotropin subunit beta 3	Homo sapiens	27-35
8524845-1	1995	Golgi alpha-mannosidase II (alpha-MII) is an enzyme involved in the processing of N-linked glycans.	n-linked glycans	82-98	mannosidase alpha class 2A member 1	Homo sapiens	0-26
7500048-3	1995	Although calnexin association with several membrane glycoproteins depends on interactions involving N-linked glycans, we previously reported that a truncation mutant of mouse Ii (mIi1-107) lacking both N-glycosylation sites was highly effective in associating with MHC class II heterodimers and escorting these dimers through the secretory pathway.	n-linked glycans	100-116	calnexin	Mus musculus	9-17
7538125-6	1995	However, coexpression of the hCG-alpha gene enhanced folding and formation of disulfide bonds 23-72, 93-100, and 26-110 of hCG-beta lacking N-linked glycans.	n-linked glycans	140-156	chromogranin A	Homo sapiens	29-38
7795417-4	1995	The bulk of the N-linked glycans of hyaluronidase consisted of small oligosaccharides (Man1-3GlcNAc2), most of which were either alpha 1,3-monofucosylated or alpha 1,3-(alpha 1,6-)difucosylated at the innermost GlcNAc residue.	n-linked glycans	16-32	hyaluronidase	Apis mellifera	36-49
7867650-6	1995	The decrease in bioactivity caused by desialylation of hCG was only restored upon alpha 6-sialylation of the Gal beta 1-->4GlcNAc beta 1-->-2Man alpha 1-->3Man branch of the N-linked glycans.	n-linked glycans	183-199	chorionic gonadotropin subunit beta 5	Homo sapiens	55-58
7929059-10	1994	In addition to the O-linked glycans, both components in the sAP complex contained N-linked glycans.	n-linked glycans	82-98	SH2 domain containing 1A	Homo sapiens	60-63
7523139-0	1994	Induction of HIV-1 envelope (gp120)-specific cytotoxic T lymphocyte responses in mice by recombinant CHO cell-derived gp120 is enhanced by enzymatic removal of N-linked glycans.	n-linked glycans	160-176	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	29-34
7523139-0	1994	Induction of HIV-1 envelope (gp120)-specific cytotoxic T lymphocyte responses in mice by recombinant CHO cell-derived gp120 is enhanced by enzymatic removal of N-linked glycans.	n-linked glycans	160-176	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	118-123
7523139-9	1994	However, envelope-specific CD8+ CTL activity was elicited when N-linked glycans were removed by treatment with an endoglycosidase.	n-linked glycans	63-79	CD8a molecule	Homo sapiens	27-30
7530195-8	1995	These data thus show that N-linked glycans play their most important role in the folding component of the folding and assembly pathway for hCG-beta.	n-linked glycans	26-42	chorionic gonadotropin subunit beta 3	Homo sapiens	139-147
7927504-5	1994	Myeloma IgA1 and IgA2 proteins and secretory IgA had higher C3b-binding activity than normal serum IgA, and this was further increased by removal of sialic acid and N-linked glycans.	n-linked glycans	165-181	immunoglobulin heavy constant alpha 1	Homo sapiens	8-12
7927504-5	1994	Myeloma IgA1 and IgA2 proteins and secretory IgA had higher C3b-binding activity than normal serum IgA, and this was further increased by removal of sialic acid and N-linked glycans.	n-linked glycans	165-181	complement C3	Homo sapiens	60-63
1385399-3	1992	We have defined an important role for the N-linked glycans attached to Asn65 of this domain in mediating CD2-CD58 interactions and also characterize its N-glycotype structure.	n-linked glycans	42-58	CD2 molecule	Homo sapiens	105-108
8129620-0	1994	Identification of three N-linked glycans in the V4-V5 region of HIV-1 gp 120, dispensable for CD4-binding and fusion activity of gp 120.	n-linked glycans	24-40	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	70-76
8129620-0	1994	Identification of three N-linked glycans in the V4-V5 region of HIV-1 gp 120, dispensable for CD4-binding and fusion activity of gp 120.	n-linked glycans	24-40	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	129-135
8129620-1	1994	Site-directed mutagenesis was used to study the biological significance of three N-linked glycans (linked to Asn406, Asn448, and Asn463), situated in the CD4-binding region of gp120.	n-linked glycans	81-97	CD4 molecule	Homo sapiens	154-157
8129620-1	1994	Site-directed mutagenesis was used to study the biological significance of three N-linked glycans (linked to Asn406, Asn448, and Asn463), situated in the CD4-binding region of gp120.	n-linked glycans	81-97	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	176-181
8129620-6	1994	All mutated gp120 species had the expected electrophoretical mobility as anticipated from elimination of one, two, and three N-linked glycans, respectively.	n-linked glycans	125-141	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	12-17
8382038-3	1993	The PdU-induced changes in N-linked glycans, released by pronase digestion of the HSV-specified glycoprotein gC-1, were investigated by using lectin affinity chromatography and Bio-Gel P6 gel filtration of glycans, radiolabelled with [3H]galactose or [3H]glucosamine.	n-linked glycans	27-43	guanylate cyclase 2e	Mus musculus	109-113
7832633-1	1994	Glycosylation is necessary for HIV-1 gp120 to attain a functional conformation, and individual N-linked glycans of gp120 are important, but not essential, for replication of HIV-1 in cell culture.	n-linked glycans	95-111	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	115-120
7937345-2	1994	Treatment of the receptor with glycopeptidase F generated a protein with a M(r) of 51,000, indicating that the GLP-1 receptor contains N-linked glycans.	n-linked glycans	135-151	glucagon-like peptide 1 receptor	Rattus norvegicus	111-125
8497042-1	1993	The role of three N-linked glycans which are conserved among various hemagglutinin (HA) subtypes of influenza A viruses was investigated by eliminating the conserved glycosylation (cg) sites at asparagine residues 12 (cg1), 28 (cg2), and 478 (cg3) by site-directed mutagenesis.	n-linked glycans	18-34	transmembrane protein 245	Homo sapiens	228-231
1281869-0	1992	Carbohydrate determinant NeuAc-Gal beta (1-4) of N-linked glycans modulates the antigenic activity of human immunodeficiency virus type 1 glycoprotein gp120.	n-linked glycans	49-65	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	151-156
1281869-1	1992	In the present study we investigated to what extent the peripheral carbohydrate structure of N-linked glycans influences the antigenic properties of human immunodeficiency virus type 1 glycoprotein 120 (gp120).	n-linked glycans	93-109	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	203-208
1429599-4	1992	Analysis on IEF was combined with a neuraminidase protection assay, in which sialic acid modification of the N-linked glycans present on Tfr and Class I molecules is used as a reporter group for cell surface expression.	n-linked glycans	109-125	transferrin receptor	Homo sapiens	137-140
1385399-3	1992	We have defined an important role for the N-linked glycans attached to Asn65 of this domain in mediating CD2-CD58 interactions and also characterize its N-glycotype structure.	n-linked glycans	42-58	CD58 molecule	Homo sapiens	109-113
1721027-6	1991	Complex-type N-linked glycans are not required for ELAM-1 mediated adhesion, and therefore the ligand for ELAM-1 is most likely a glycolipid, or a glycoprotein carrying O-linked oligosaccharides.	n-linked glycans	13-29	selectin E	Homo sapiens	106-112
1396689-4	1992	Porcine thyroglobulin was shown to carry the mannose 6-phosphate-(Man6P)-recognition marker on its N-linked glycans.	n-linked glycans	99-115	thyroglobulin	Homo sapiens	8-21
1627608-5	1992	The results showed that N-linked glycans on placental syncytiotrophoblast and cytotrophoblast, kidney and platelet MCP are similar in binding to concanavalin A and Lens culinaris lectins, but are not bound by leucophytohemagglutinin.	n-linked glycans	24-40	CD46 molecule	Homo sapiens	115-118
1371154-0	1992	Detection of multisulphated N-linked glycans in the L2/HNK-1 carbohydrate epitope expressing neural adhesion molecule P0.	n-linked glycans	28-44	beta-1,3-glucuronyltransferase 1	Homo sapiens	55-60
1744125-3	1991	Purified betaglycan has properties similar to betaglycan affinity-labeled in intact cells: it binds TGF-beta 1 and TGF-beta 2 with KD approximately 0.2 nM, contains heparan sulfate and chondroitin sulfate glycosaminoglycan (GAG) chains and N-linked glycans attached to a 110-kDa core protein, and can spontaneously associate with phosphatidylcholine liposomes.	n-linked glycans	240-256	transforming growth factor beta receptor 3	Rattus norvegicus	9-19
1710649-11	1991	Two recombinant NS1 forms were detected in insect cells: a major one with an apparent Mr of 48K and a minor one of 47K in which N-linked glycans were probably processed to a trimannosyl core without further elongation.	n-linked glycans	128-144	influenza virus NS1A binding protein	Homo sapiens	16-19
1895386-6	1991	The gs3- mutation affected a second posttranslational modification of unknown type, which was manifested as production of gp70 that remained smaller than wild-type gp70 after removal of all N-linked glycans by peptide N-glycosidase F. The gs4- mutation decreased processing of gPr80 to gPr90, completely inhibited proteolytic processing of gPr90 to gp70 and Pr15(E), and prevented incorporation of envelope products into virus particles.	n-linked glycans	190-206	DnaJ heat shock protein family (Hsp40) member C21	Homo sapiens	4-7
1895386-6	1991	The gs3- mutation affected a second posttranslational modification of unknown type, which was manifested as production of gp70 that remained smaller than wild-type gp70 after removal of all N-linked glycans by peptide N-glycosidase F. The gs4- mutation decreased processing of gPr80 to gPr90, completely inhibited proteolytic processing of gPr90 to gp70 and Pr15(E), and prevented incorporation of envelope products into virus particles.	n-linked glycans	190-206	embigin	Homo sapiens	122-126
2335819-1	1990	We have shown that enzymatic removal of N-linked glycans from human immunodeficiency virus type 1 (HIV-1) recombinant envelope glycoproteins gp160 and gp120 produced in BHK-21 cells did not significantly reduce their ability to bind to CD4, the cellular receptor for the virus.	n-linked glycans	40-56	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	141-146
2335819-1	1990	We have shown that enzymatic removal of N-linked glycans from human immunodeficiency virus type 1 (HIV-1) recombinant envelope glycoproteins gp160 and gp120 produced in BHK-21 cells did not significantly reduce their ability to bind to CD4, the cellular receptor for the virus.	n-linked glycans	40-56	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	151-156
2335819-1	1990	We have shown that enzymatic removal of N-linked glycans from human immunodeficiency virus type 1 (HIV-1) recombinant envelope glycoproteins gp160 and gp120 produced in BHK-21 cells did not significantly reduce their ability to bind to CD4, the cellular receptor for the virus.	n-linked glycans	40-56	T-cell surface glycoprotein CD4	Mesocricetus auratus	236-239
34806177-2	2022	N-acetylglucosaminyltransferase V (GnT-V) is the Golgi enzyme, and it has been reported that the beta1,6GlcNAc-branched N-linked glycans are associated with various cell behaviors.	n-linked glycans	120-136	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	0-33
34860526-6	2022	A formalin-fixed paraffin-embedded human prostate tissue was analyzed in negative ionization mode after tissue washing, antigen retrieval, and pneumatic application of PNGase F for enzymatic digestion of N-linked glycans.	n-linked glycans	204-220	N-glycanase 1	Homo sapiens	168-174
34863021-0	2022	Removal of single-site N-linked glycans on factor VIII alters binding of domain-specific monoclonal antibodies.	n-linked glycans	23-39	coagulation factor VIII	Mus musculus	43-54
34863021-10	2022	CONCLUSIONS: Modifications of FVIII N-linked glycans reduced FVIII endocytosis by BMDCs and binding of domain-specific FVIII MAbs, but did not alter de novo antibody production in hemophilia A mice suggesting that N-glycans do not significantly contribute to inhibitor formation.	n-linked glycans	36-52	coagulation factor VIII	Mus musculus	61-66
34863021-10	2022	CONCLUSIONS: Modifications of FVIII N-linked glycans reduced FVIII endocytosis by BMDCs and binding of domain-specific FVIII MAbs, but did not alter de novo antibody production in hemophilia A mice suggesting that N-glycans do not significantly contribute to inhibitor formation.	n-linked glycans	36-52	coagulation factor VIII	Mus musculus	119-124
34806177-2	2022	N-acetylglucosaminyltransferase V (GnT-V) is the Golgi enzyme, and it has been reported that the beta1,6GlcNAc-branched N-linked glycans are associated with various cell behaviors.	n-linked glycans	120-136	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	35-40
34995415-1	2022	The pan-caspase inhibitor Z-VAD-fmk acts as an inhibitor of peptide:N-glycanase (NGLY1); an endoglycosidase which cleaves N-linked glycans from glycoproteins exported from the endoplasmic reticulum (ER) during ER-associated degradation (ERAD).	n-linked glycans	122-138	N-glycanase 1	Homo sapiens	81-86
34494876-3	2021	Previous work has demonstrated the presence of N-linked glycans in ACE2.	n-linked glycans	47-63	angiotensin converting enzyme 2	Homo sapiens	67-71
34213308-2	2021	The abundance of N-linked glycans across the SARS-CoV-2 spike protein is a potential source of heterogeneity among the many different vaccine candidates under investigation.	n-linked glycans	17-33	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	56-61
35470665-1	2022	Dense glycosylation and the trimeric conformation of the human immunodeficiency virus-1 (HIV-1) envelope protein limit the accessibility of some cellular glycan processing enzymes and end up with high-mannose-type N-linked glycans on the envelope spike, among which the Man5GlcNAc2 structure occupies a certain proportion.	n-linked glycans	214-230	endogenous retrovirus group K member 6, envelope	Homo sapiens	96-112
35188715-2	2022	A remarkable feature of ACPA-IgG is the abundant expression of N-linked glycans in the variable domain.	n-linked glycans	63-79	proteinase 3	Homo sapiens	24-28
35467485-1	2022	Dolichyl-phosphate N-acetylglucosaminephosphotransferase (dpagt1) inhibition is reported to kill tumor cells whose growth progression requires increased branching of N-linked glycans.	n-linked glycans	166-182	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Homo sapiens	58-64
35311117-5	2022	Mechanistically, we showed that STT3A transferred N-linked glycans to PD-L1, and TGF-beta1 could positively regulate STT3A expression through activating c-Jun to bind to STT3A promoter.	n-linked glycans	50-66	STT3 oligosaccharyltransferase complex catalytic subunit A	Homo sapiens	32-37
35311117-5	2022	Mechanistically, we showed that STT3A transferred N-linked glycans to PD-L1, and TGF-beta1 could positively regulate STT3A expression through activating c-Jun to bind to STT3A promoter.	n-linked glycans	50-66	Jun proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	153-158
35509261-2	2022	A single alpha-(1,6)-fucosyltransferase (FUT8) is responsible for catalyzing the addition of an alpha-1,6-linked fucose residue to the first GlcNAc residue of the N-linked glycans.	n-linked glycans	163-179	alpha-(1,6)-fucosyltransferase	Cricetulus griseus	9-39
35509261-2	2022	A single alpha-(1,6)-fucosyltransferase (FUT8) is responsible for catalyzing the addition of an alpha-1,6-linked fucose residue to the first GlcNAc residue of the N-linked glycans.	n-linked glycans	163-179	alpha-(1,6)-fucosyltransferase	Cricetulus griseus	41-45
35406718-1	2022	N-Glycanase 1 (NGLY1) is a cytosolic enzyme involved in removing N-linked glycans of misfolded N-glycoproteins and is considered to be a component of endoplasmic reticulum-associated degradation (ERAD).	n-linked glycans	65-81	N-glycanase 1	Homo sapiens	0-13
35406718-1	2022	N-Glycanase 1 (NGLY1) is a cytosolic enzyme involved in removing N-linked glycans of misfolded N-glycoproteins and is considered to be a component of endoplasmic reticulum-associated degradation (ERAD).	n-linked glycans	65-81	N-glycanase 1	Homo sapiens	15-20
35178035-4	2021	We show that YadA from Y. enterocolitica serotype O:9 does not interact with the vitronectin protein itself but exclusively with its N-linked glycans.	n-linked glycans	133-149	Adhesin	Yersinia enterocolitica	13-17