doc_id	sent_index	relation_id	relation	trigger	trigger_offset	arg_num	arg_base_np	arg_protein	arg_domain	arg_site	arg_sugar	PSource	SiteSource	NProtein	NID	SiteName	sent_text
26553286	3	62	gly	glycoprotein	568:579	arg1	often a glycoprotein	often a glycoprotein				PUBTATOR		a glycoprotein	351		The synthesis of (neo)glycoconjugates with bi- to oligo-valency (glycoclusters) affords tools to delineate structure-activity relationships by blocking lectin binding to an artificial matrix, often a glycoprotein, or cultured cell lines.
26704999	4	58	gly	possessed	449:457	arg1	PGP AND sugar composition	PGP			sugar composition	OGER		PGP	A6NDG6		Data indicated that PGP possessed sugar composition of rhamnose (2%), arabinose (3%), mannose (3%), galactose (94%) and uronic acid (17%) confirming that PGP thus isolated is a galactan.
28514686	1	50	gly	glycoprotein	171:182	arg1	Env	Env				Cterm		Env	155971		Advances in HIV-1 envelope glycoprotein (Env) design generate native-like trimers and high-resolution clade A, B, and G structures and elicit neutralizing antibodies.
28514686	1	50	gly	glycoprotein	171:182	arg1	HIV-1 envelope glycoprotein	HIV-1 envelope glycoprotein				PUBTATOR		envelope glycoprotein	155971		Advances in HIV-1 envelope glycoprotein (Env) design generate native-like trimers and high-resolution clade A, B, and G structures and elicit neutralizing antibodies.
25726973	0	13	gly	glycoprotein	90:101	arg1	porcine reproductive and respiratory syndrome virus envelope glycoprotein 5	porcine reproductive and respiratory syndrome virus envelope glycoprotein 5				PUBTATOR		envelope glycoprotein 5	155971		N-glycosylation profiling of porcine reproductive and respiratory syndrome virus envelope glycoprotein 5.
26686161	1	56	gly	HN1	237:239	arg1	mycelial polysaccharides	HN1			mycelial polysaccharides	OGER		HN1	Q9UK76		Optimization of extraction, characterization and antioxidant activity of mycelial polysaccharides from Paecilomyces hepiali HN1 (PHMPs) were investigated.
29556562	0	64	gly	highly-glycosylated	51:69	arg1	a highly-glycosylated peroxidase	a highly-glycosylated peroxidase				PUBTATOR		peroxidase	548137		Zo-peroxidase: Crystal structure and sequence of a highly-glycosylated peroxidase resistant to high concentrations of H2O2 from Japanese radish.
29108390	1	76	gly	glycosylated	232:243	arg1	Tn-antigen	Tn-antigen				PUBTATOR		Tn-antigen, sTn	1917		Truncated O-glycans, including Tn-antigen, sTn-antigen, T-antigen, sT-antigen, are incomplete glycosylated structures and their expression occur frequently in tumor tissue.
26109728	14	0	gly	glycoprotein	2211:2222	arg1	the virus envelope glycoprotein	the virus envelope glycoprotein				PUBTATOR		envelope glycoprotein	100616444		The V3 loop is one of the few immunogenic targets on the virus envelope glycoprotein that can induce neutralizing antibodies, but in many viruses, parts of V3 are inaccessible for antibody recognition.
26483702	2	58	gly	glycosylated	270:281	arg1	Native UT-A1	Native UT-A1				PUBTATOR		Native UT-A1	27411		Native UT-A1 from kidney inner medulla (IM) is a heavily glycosylated protein with two glycosylation forms of 97 and 117 kDa.
28347786	3	55	gly	had	471:473	arg1	all GPs AND the typical saccharide absorptions	all GPs			the typical saccharide absorptions	OGER		GPs			The results revealed that all GPs had the typical saccharide absorptions, and all were heteropolysaccharides.
26791584	2	44	gly	PAL	239:241	arg1	glucose	PAL			glucose	OGER		PAL	Q9P2V4		The primary monosaccharide composition of the PAL was determined to be glucose, where HPAEC analysis showed no significant amount of any other sugars.
26791584	2	44	gly	PAL	239:241	arg1	The primary monosaccharide composition	PAL			The primary monosaccharide composition	OGER		PAL	Q9P2V4		The primary monosaccharide composition of the PAL was determined to be glucose, where HPAEC analysis showed no significant amount of any other sugars.
25211026	9	62	gly	PrP	1403:1405	arg1	de-sialylation	PrP			de-sialylation	PUBTATOR		PrP	19122		Moreover, de-sialylation of PrP(C) reduced or eliminated a species barrier of for prion amplification in PMCAb.
25211026	9	85	gly	de-sialylation	1385:1398	arg1	C	C				Cterm		C	19122		Moreover, de-sialylation of PrP(C) reduced or eliminated a species barrier of for prion amplification in PMCAb.
25211026	9	85	gly	de-sialylation	1385:1398	arg1	PrP	PrP				PUBTATOR		PrP	19122		Moreover, de-sialylation of PrP(C) reduced or eliminated a species barrier of for prion amplification in PMCAb.
25726973	2	15	gly	glycoprotein	303:314	arg1	GP5	GP5				PUBTATOR		5 (GP5	2814		Glycans of major envelope glycoprotein 5 (GP5) are proposed as important for virus assembly and entry into permissive cells.
25726973	2	27	gly	glycoprotein	303:314	arg1	Glycans	envelope glycoprotein 5			Glycans	PUBTATOR		envelope glycoprotein 5	155971		Glycans of major envelope glycoprotein 5 (GP5) are proposed as important for virus assembly and entry into permissive cells.
25124516	0	8	gly	disialylated	65:76	arg1	disialylated IgG	disialylated IgG				Cterm		IgG			Filariasis asymptomatically infected donors have lower levels of disialylated IgG compared to endemic normals.
26337523	2	78	gly	SPS-CF	1206:1211	arg1	xylose	SPS			xylose	OGER		SPS	P49903		However, the results of the present study re-performed for monosaccharide composition of this polysaccharide using, in addition to HPLC of PMP-labelled sugars, other separation methods, i.e. high-performance anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD), gas chromatography with flame ionising detection (GC-FID) and thin-layer chromatography (TLC), clearly demonstrated that the most prominent neutral monosaccharides of SPS-CF are xylose (38.6-49.4 mol %) and rhamnose (39.6-45 mol %), while mannose and galactose are present at a much lesser extent or in negligible amount.
26337523	2	78	gly	SPS-CF	1206:1211	arg1	the most prominent neutral monosaccharides	SPS			the most prominent neutral monosaccharides	OGER		SPS	P49903		However, the results of the present study re-performed for monosaccharide composition of this polysaccharide using, in addition to HPLC of PMP-labelled sugars, other separation methods, i.e. high-performance anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD), gas chromatography with flame ionising detection (GC-FID) and thin-layer chromatography (TLC), clearly demonstrated that the most prominent neutral monosaccharides of SPS-CF are xylose (38.6-49.4 mol %) and rhamnose (39.6-45 mol %), while mannose and galactose are present at a much lesser extent or in negligible amount.
28620376	3	69	gly	Fc-glycosylation	453:468	arg1	IgG effector functions	IgG effector functions				PUBTATOR		IgG	668542		The mouse is often used as experimental animal model to study the effects of Fc-glycosylation on IgG effector functions, and results are not uncommonly translated back to the human situation.
25211026	2	136	gly	sialoglycoprotein	347:363	arg1	Pr	Pr				PUBTATOR		Pr(PC	19122		Pr(PC) is a sialoglycoprotein that contains two conserved N-glycosylation sites.
28602514	4	26	gly	cell-surface/ECM	750:765	arg1	proteoglycans	ECM			proteoglycans	OGER		ECM	Q13201		Based on this observation, we have investigated here the effects of JAD on proteoglycans and glycosaminoglycan (GAG) polysaccharides, which are major cell-surface/ECM components and are involved in a multitude of biological processes.
28602514	4	26	gly	cell-surface/ECM	750:765	arg1	glycosaminoglycan (GAG) polysaccharides	ECM			glycosaminoglycan (GAG) polysaccharides	OGER		ECM	Q13201		Based on this observation, we have investigated here the effects of JAD on proteoglycans and glycosaminoglycan (GAG) polysaccharides, which are major cell-surface/ECM components and are involved in a multitude of biological processes.
26359989	3	10	gly	glycosylated	571:582	arg1	fully glycosylated Env trimer	fully glycosylated Env trimer				PUBTATOR		Env trimer	100616444		To investigate 8ANC195's gp41 epitope at higher resolution, we solved a 3.58 Å crystal structure of 8ANC195 complexed with fully glycosylated Env trimer, revealing 8ANC195 insertion into a glycan shield gap to contact gp120 and gp41 glycans and protein residues.
28433181	2	15	gly	SPS2p	418:422	arg1	the monosaccharide composition	SPS2p			the monosaccharide composition	PUBTATOR		SPS2p	22928		The molecular weight of SPS2p showed only one molecular weight distribution (2.6×104Da) and the monosaccharide composition of SPS2p showed the presence of arabinose, mannose, glucose and galactose at the ratio of 1.31:1.00:3.59:1.59.
25211026	6	81	gly	sialylated	1055:1064	arg1	Sc	Sc				Cterm		Sc	19122		As a result, PMCAb-derived PrP(Sc) was less sialylated than brain-derived PrP(Sc).
25211026	6	81	gly	sialylated	1055:1064	arg1	PMCAb-derived PrP	PMCAb-derived PrP				PUBTATOR		PrP	19122		As a result, PMCAb-derived PrP(Sc) was less sialylated than brain-derived PrP(Sc).
24721094	5	17	gly	JSP1	663:666	arg1	three polysaccharide fractions	JSP1			three polysaccharide fractions	PUBTATOR		JSP1	56940		After precipitation with ethanol at final concentration of 40%, 60% and 80% in turn, three polysaccharide fractions of JSP1, JSP2 and JSP3 were obtained from JSP, respectively.
25915761	6	53	gly	modified	824:831	arg1	Secreted HIV-1 gp140 AND mainly monosialylated core 1 O-glycans	Secreted HIV-1 gp140			mainly monosialylated core 1 O-glycans	Cterm		1 gp140			Secreted HIV-1 gp140 was modified to a lesser extent with mainly monosialylated core 1 O-glycans, suggesting that the ectodomain of the gp41 transmembrane component may limit the accessibility of Thr499 to glycosyltransferases.
25915761	8	67	gly	carbohydrates	1233:1245	arg1	Thr499			Thr499	Thr499		AminoAcid			Thr499	Our results indicate the absence of O-linked carbohydrates on Thr499 as it exists on the surface of virions and suggest caution in the interpretation of analyses of post-translational modifications that utilize recombinant forms of envelope protein.
28620376	5	32	gly	glycosylation	724:736	arg1	murine IgG-Fc	murine IgG-Fc				PUBTATOR		IgG	668542		To characterize the glycosylation profile of murine IgG-Fc and in addition evaluate the systematic glycosylation differences between mouse strains, sexes, and IgG subclasses, we used nanoliquid chromatography mass spectrometry (nanoLC-MS(/MS)) to look at the subclass-specific IgG Fc-glycopeptides of male and female mice from the strains BALB/c, C57BL/6, CD-1, and Swiss Webster.
28620376	5	86	gly	Fc-glycopeptides	985:1000	arg1	CD-1	C57BL/6, CD-1				PUBTATOR		C57BL/6, CD-1	111334		To characterize the glycosylation profile of murine IgG-Fc and in addition evaluate the systematic glycosylation differences between mouse strains, sexes, and IgG subclasses, we used nanoliquid chromatography mass spectrometry (nanoLC-MS(/MS)) to look at the subclass-specific IgG Fc-glycopeptides of male and female mice from the strains BALB/c, C57BL/6, CD-1, and Swiss Webster.
26190688	7	20	gly	chain	957:961	arg1	→6)-β-D-Glcp-(1→ side chain	chain			→6)-β-D-Glcp-(1→ side chain	OGER		chain	16193		The two-dimensional COSY, NOESY and TOCSY confirmed that these polysaccharides have a main chain of →3)-β-D-Glcp-(1→ with →6)-β-D-Glcp-(1→ side chain.
25211026	8	58	gly	de-sialylation	1215:1228	arg1	C	C				Cterm		C	19122		Nevertheless, enzymatic de-sialylation of PrP(C) using sialidase was found to increase the rate of PrP(Sc) amplification in PMCAb from 10- to 10,000-fold in a strain-dependent manner.
25211026	8	58	gly	de-sialylation	1215:1228	arg1	PrP	PrP				PUBTATOR		PrP	19122		Nevertheless, enzymatic de-sialylation of PrP(C) using sialidase was found to increase the rate of PrP(Sc) amplification in PMCAb from 10- to 10,000-fold in a strain-dependent manner.
25211026	8	132	gly	PrP	1233:1235	arg1	enzymatic de-sialylation	PrP			enzymatic de-sialylation	PUBTATOR		PrP	19122		Nevertheless, enzymatic de-sialylation of PrP(C) using sialidase was found to increase the rate of PrP(Sc) amplification in PMCAb from 10- to 10,000-fold in a strain-dependent manner.
24057866	2	78	gly	Lewis	437:441	arg1	AAL-reactive core fucose	Lewis(			AAL-reactive core fucose	PUBTATOR		Lewis(	2526		The seminal IgG and SC are decorated with AAL-reactive core fucose, and antennary UEA- and LTA-reactive fucose of Lewis(y) and Lewis(x) structures, respectively.
24057866	2	78	gly	Lewis	437:441	arg1	LTA-reactive fucose	Lewis(			LTA-reactive fucose	PUBTATOR		Lewis(	2526		The seminal IgG and SC are decorated with AAL-reactive core fucose, and antennary UEA- and LTA-reactive fucose of Lewis(y) and Lewis(x) structures, respectively.
28356486	1	23	gly	contained	440:448	arg1	decorin AND biglycan	decorin			biglycan	PUBTATOR		SLRPs) decorin	1634		In a recent publication in Bioscience Reports "Contaminants in commercial preparations of 'purified' small leucine-rich proteoglycans may distort mechanistic studies", Brown et al. identified by mass spectrometry and immunoblotting that certain commercial preparations of the small leucine-rich proteoglycans (SLRPs) decorin and biglycan, in fact, contained a mix of several proteoglycans that also included fibromodulin and aggrecan.
26454110	1	20	gly	GPS	277:279	arg1	a water-soluble polysaccharide	GPS			a water-soluble polysaccharide	OGER		GPS			To contribute toward effective exploitation and utilization of spent mushroom compost (SMC) of Ganoderma lucidum (SMC-G), a water-soluble polysaccharide of GPS was extracted, and then two fractions (GPS-1 and GPS-2) were purified from SMC-G.
25211026	0	24	gly	glycoform	117:125	arg1	PrPSc glycoform	PrPSc glycoform				PUBTATOR		PrPSc	19122		Sialylation of prion protein controls the rate of prion amplification, the cross-species barrier, the ratio of PrPSc glycoform and prion infectivity.
27259648	1	17	gly	IPS-1	188:192	arg1	the intracellular polysaccharide (IPS)	IPS-1			the intracellular polysaccharide (IPS)	OGER		IPS-1	Q9NPH2		In present study, the intracellular polysaccharide (IPS) and its two fractions of IPS-1 and IPS-2 were obtained and purified by DEAE-52 cellulose chromatography from Pleurotus eryngii SI-04 mycelia, and their hepatoprotective effects were also investigated.
27402833	1	25	gly	glycosylated	109:120	arg1	The HIV-1 envelope glycoprotein gp120	The HIV-1 envelope glycoprotein gp120				PUBTATOR		gp120	3700		The HIV-1 envelope glycoprotein gp120 is heavily glycosylated and bears numerous high mannose sugars.
27402833	1	56	gly	bears	126:130	arg1	The HIV-1 envelope glycoprotein gp120 AND numerous high mannose sugars	The HIV-1 envelope glycoprotein gp120			numerous high mannose sugars	PUBTATOR		gp120	3700		The HIV-1 envelope glycoprotein gp120 is heavily glycosylated and bears numerous high mannose sugars.
26731606	0	42	gly	Glycosylation	0:12	arg1	SOS5	SOS5				PUBTATOR		SOS5	823808		Glycosylation of a Fasciclin-Like Arabinogalactan-Protein (SOS5) Mediates Root Growth and Seed Mucilage Adherence via a Cell Wall Receptor-Like Kinase (FEI1/FEI2) Pathway in Arabidopsis.
26731606	0	42	gly	Glycosylation	0:12	arg1	a Fasciclin-Like Arabinogalactan-Protein	a Fasciclin-Like Arabinogalactan-Protein				PUBTATOR		Fasciclin-Like Arabinogalactan-Protein	829121		Glycosylation of a Fasciclin-Like Arabinogalactan-Protein (SOS5) Mediates Root Growth and Seed Mucilage Adherence via a Cell Wall Receptor-Like Kinase (FEI1/FEI2) Pathway in Arabidopsis.
25046106	10	15	gly	NSP	1920:1922	arg1	xylose	NSP			xylose	OGER		NSP	O95405		The total amount of digested NSP (r=0.57; P=0.002), xylose (r=0.53; P=0.004) and dietary fiber (r=0.60; P=0.001) in ileal digesta were positively correlated with an increased abundance of Bacteroides-Prevotella-Porphyromonas.
25421533	6	27	gly	contained	864:872	arg1	EPA AND polysaccharides	EPA			polysaccharides	OGER		EPA	P01033		EPA contained polyphenols, flavonoids and polysaccharides, with polysaccharide content at least 26 times greater than that of polyphenols and flavonoids.
28807689	3	28	gly	AVP	582:584	arg1	d-galactose	AVP			d-galactose	PUBTATOR		AVP	551		The main monosaccharide compositions of AVP were d-galactose, d-xylose, d-mannose, d-glucose and d-glucuronic acid.
28807689	3	28	gly	AVP	582:584	arg1	The main monosaccharide compositions	AVP			The main monosaccharide compositions	PUBTATOR		AVP	551		The main monosaccharide compositions of AVP were d-galactose, d-xylose, d-mannose, d-glucose and d-glucuronic acid.
24057866	0	48	gly	IgG	41:43	arg1	fucosylation	IgG			fucosylation	Cterm		IgG			Changes in fucosylation of human seminal IgG and secretory component of IgA in leukocytospermic patients.
24057866	0	95	gly	fucosylation	11:22	arg1	human seminal IgG	human seminal IgG				Cterm		IgG			Changes in fucosylation of human seminal IgG and secretory component of IgA in leukocytospermic patients.
25211026	11	0	gly	PrP	1667:1669	arg1	the sialylation status	PrP			the sialylation status	PUBTATOR		PrP	19122		Surprisingly, the sialylation status of PrP(C) was also found to control PrP(Sc) glycoform ratio.
25211026	11	20	gly	sialylation	1645:1655	arg1	PrP	PrP				PUBTATOR		PrP	19122		Surprisingly, the sialylation status of PrP(C) was also found to control PrP(Sc) glycoform ratio.
25211026	11	20	gly	sialylation	1645:1655	arg1	C	C				Cterm		C	19122		Surprisingly, the sialylation status of PrP(C) was also found to control PrP(Sc) glycoform ratio.
24559734	6	3	gly	galactose	1155:1163	arg1	the ratio 2:2:1	2:1			galactose	OGER		2:1	P35326		On the other hand, the pellicle polysaccharides of SL13E-3 and SKU1108 strains are composed of rhamnose, glucose and galactose in the ratio 2:2:1 and 1:5:2.5, respectively.
24559734	6	16	gly	rhamnose	1133:1140	arg1	the ratio 2:2:1	2:1			rhamnose	OGER		2:1	P35326		On the other hand, the pellicle polysaccharides of SL13E-3 and SKU1108 strains are composed of rhamnose, glucose and galactose in the ratio 2:2:1 and 1:5:2.5, respectively.
24559734	6	23	gly	glucose	1143:1149	arg1	the ratio 2:2:1	2:1			glucose	OGER		2:1	P35326		On the other hand, the pellicle polysaccharides of SL13E-3 and SKU1108 strains are composed of rhamnose, glucose and galactose in the ratio 2:2:1 and 1:5:2.5, respectively.
29166575	2	8	gly	presence	566:573	arg2	CGE AND polysaccharides	CGE			polysaccharides	OGER		CGE	A0A0U1RPR8		AIM OF THE STUDY In the present study, we aimed at forming a chemical characterization and investigation of the antinociceptive and anti-inflammatory activities of the aqueous extract of cashew gum without the presence of polysaccharides in its composition (CGE).
25124516	7	31	gly	disialylated	1422:1433	arg1	disialylated IgG	disialylated IgG				Cterm		IgG			Using capillary electrophoresis, we found that there was no difference in galactosylation of total IgG between the three groups; however, asymptomatically infected patients had significantly lower levels of disialylated IgG compared to endemic normals and patients with pathology.
29430281	1	51	gly	isolated	385:392	arg1	SMS AND hot-water-extractable polysaccharides	SMS			hot-water-extractable polysaccharides	OGER		SMS	P52788		In order to contribute to the exploitation and utilization of spent mushroom substrates (SMS) of Laetiporus sulphureus, hot-water-extractable polysaccharides (H-SMPS) and enzymatic-extractable polysaccharides (E-SMPS) were successfully isolated from SMS of L. sulphureus.
29430281	1	51	gly	isolated	385:392	arg1	SMS AND enzymatic-extractable polysaccharides	SMS			enzymatic-extractable polysaccharides	OGER		SMS	P52788		In order to contribute to the exploitation and utilization of spent mushroom substrates (SMS) of Laetiporus sulphureus, hot-water-extractable polysaccharides (H-SMPS) and enzymatic-extractable polysaccharides (E-SMPS) were successfully isolated from SMS of L. sulphureus.
28347786	2	39	gly	GPs	356:358	arg1	monosaccharide compositions	GPs			monosaccharide compositions	OGER		GPs			The chemical characterization and monosaccharide compositions of GPs, named as GP-1, GP-2, GP-3, and GP-4, were determined by PMP-HPLC and FT-IR.
28390831	5	38	gly	presence	552:559	arg2	ANG AND rhamnose	ANG			rhamnose	OGER		ANG	P03950		The sugar composition of the gums indicated the presence of arabinose, galactose, and rhamnose in ANG and AG.
28390831	5	38	gly	presence	552:559	arg2	ANG AND galactose	ANG			galactose	OGER		ANG	P03950		The sugar composition of the gums indicated the presence of arabinose, galactose, and rhamnose in ANG and AG.
28390831	5	38	gly	presence	552:559	arg2	ANG AND arabinose	ANG			arabinose	OGER		ANG	P03950		The sugar composition of the gums indicated the presence of arabinose, galactose, and rhamnose in ANG and AG.
26721884	11	57	gly	OS9	1584:1586	arg1	the mannose 6-phosphate receptor homology domain	OS9			the mannose 6-phosphate receptor homology domain	PUBTATOR		OS9	10956		Inactivation of the mannose 6-phosphate receptor homology domain of OS9 had no effect on its action on NKCC2.
25211026	13	53	gly	sialylation	1894:1904	arg1	C	C				Cterm		C	19122		2D analysis of charge distribution revealed that the sialylation status of brain-derived PrP(C) differed from that of spleen-derived PrP(C).
25211026	13	53	gly	sialylation	1894:1904	arg1	brain-derived PrP	brain-derived PrP				PUBTATOR		PrP	19122		2D analysis of charge distribution revealed that the sialylation status of brain-derived PrP(C) differed from that of spleen-derived PrP(C).
25211026	13	133	gly	PrP	1930:1932	arg1	the sialylation status	PrP			the sialylation status	PUBTATOR		PrP	19122		2D analysis of charge distribution revealed that the sialylation status of brain-derived PrP(C) differed from that of spleen-derived PrP(C).
27760230	7	9	gly	pssA	840:843	arg1	exopolysaccharide	pssA			exopolysaccharide	OGER		pssA	P48651		trifolii strain 24.2 and its derivatives producing various levels of exopolysaccharide (EPS), namely, pssA mutant Rt5819 deficient in EPS synthesis, rosR mutant Rt2472 producing diminished amounts of this polysaccharide, and two EPS-overproducing strains, Rt24.2(pBA1) and Rt24.2(pBR1), under different growth conditions (medium type, bacterial culture age, cell viability, and pH).
27302279	0	50	gly	Glycosylation	0:12	arg1	plasma IgG	plasma IgG				PUBTATOR		IgG	16059		Glycosylation of plasma IgG in colorectal cancer prognosis.
27474571	4	42	gly	UCP	1116:1118	arg1	monosaccharide composition	UCP (1			monosaccharide composition	OGER		UCP (1	P25874		Results showed that no considerable change was observed on the structure between the polysaccharide of Cyclocarya paliurus (CP) and the ultrasonic polysaccharide of Cyclocarya paliurus (UCP) by FT-IR, and no apparent differences were found on the content of sugar, uronic acid and protein after the ultrasonic treatment, but difference appeared in the ratio of monosaccharide composition of CP (1.0:4.6:3.5:4.5) and UCP (1.0:5.9:3.9:4.4), and the antioxidant activities of CP were promoted after ultrasonic treatment.
25211026	5	25	gly	undersialylated	857:871	arg1	C	C				Cterm		C	19122		The current study demonstrates that undersialylated PrP(C) is selected during prion amplification in Protein Misfolding Cyclic Amplification (PMCAb) at the expense of oversialylated PrP(C).
25211026	5	25	gly	undersialylated	857:871	arg1	undersialylated PrP	undersialylated PrP				PUBTATOR		PrP	19122		The current study demonstrates that undersialylated PrP(C) is selected during prion amplification in Protein Misfolding Cyclic Amplification (PMCAb) at the expense of oversialylated PrP(C).
25211026	5	93	gly	oversialylated	988:1001	arg1	C	C				Cterm		C	19122		The current study demonstrates that undersialylated PrP(C) is selected during prion amplification in Protein Misfolding Cyclic Amplification (PMCAb) at the expense of oversialylated PrP(C).
25211026	5	93	gly	oversialylated	988:1001	arg1	oversialylated PrP	oversialylated PrP				PUBTATOR		PrP	19122		The current study demonstrates that undersialylated PrP(C) is selected during prion amplification in Protein Misfolding Cyclic Amplification (PMCAb) at the expense of oversialylated PrP(C).
27449907	1	118	gly	possesses	183:191	arg1	the HIV-1 envelope protein gp120 AND a glycan-dependent epitope	the HIV-1 envelope protein gp120		two important epitopes	a glycan-dependent epitope	PUBTATOR		gp120	3700	epitopes	The V1/V2 domain of the HIV-1 envelope protein gp120 possesses two important epitopes: a glycan-dependent epitope recognized by the prototypic broadly neutralizing monoclonal antibody (bN-mAb), PG9, as well as an epitope recognized by non-neutralizing antibodies that has been associated with protection from HIV infection in the RV144 HIV vaccine trial.
25211026	14	33	gly	sialidase	2005:2013	arg1	lysosomal sialidase Neu1	lysosomal sialidase			lysosomal sialidase Neu1	OGER		lysosomal sialidase	Q99519		Knocking out lysosomal sialidase Neu1 did not change the sialylation status of brain-derived PrP(C), suggesting that Neu1 is not responsible for desialylation of PrP(C).
25211026	14	43	gly	PrP	2144:2146	arg1	desialylation	PrP			desialylation	PUBTATOR		PrP	19122		Knocking out lysosomal sialidase Neu1 did not change the sialylation status of brain-derived PrP(C), suggesting that Neu1 is not responsible for desialylation of PrP(C).
25211026	14	55	gly	sialylation	2039:2049	arg1	C	C				Cterm		C	19122		Knocking out lysosomal sialidase Neu1 did not change the sialylation status of brain-derived PrP(C), suggesting that Neu1 is not responsible for desialylation of PrP(C).
25211026	14	55	gly	sialylation	2039:2049	arg1	brain-derived PrP	brain-derived PrP				PUBTATOR		PrP	19122		Knocking out lysosomal sialidase Neu1 did not change the sialylation status of brain-derived PrP(C), suggesting that Neu1 is not responsible for desialylation of PrP(C).
25211026	14	82	gly	PrP	2075:2077	arg1	the sialylation status	PrP			the sialylation status	PUBTATOR		PrP	19122		Knocking out lysosomal sialidase Neu1 did not change the sialylation status of brain-derived PrP(C), suggesting that Neu1 is not responsible for desialylation of PrP(C).
25211026	14	91	gly	desialylation	2127:2139	arg1	PrP	PrP				PUBTATOR		PrP	19122		Knocking out lysosomal sialidase Neu1 did not change the sialylation status of brain-derived PrP(C), suggesting that Neu1 is not responsible for desialylation of PrP(C).
25211026	14	91	gly	desialylation	2127:2139	arg1	C	C				Cterm		C	19122		Knocking out lysosomal sialidase Neu1 did not change the sialylation status of brain-derived PrP(C), suggesting that Neu1 is not responsible for desialylation of PrP(C).
25211026	14	116	gly	lysosomal	1995:2003	arg1	lysosomal sialidase Neu1	lysosomal sialidase			lysosomal sialidase Neu1	OGER		lysosomal sialidase	Q99519		Knocking out lysosomal sialidase Neu1 did not change the sialylation status of brain-derived PrP(C), suggesting that Neu1 is not responsible for desialylation of PrP(C).
25104038	5	31	part_of	residues	853:860	arg1	HbCLP2	HbCLP2		residues		PUBTATOR	AminoAcid	HbCLP2	110639626	residues Glu117 and Glu147	Sequence alignments showed that in the two proteins the catalytic residues Glu117 and Glu147 in HbCLP1 and HbCLP2, respectively, were mutated to Ala, accounting for the lack of activity.
25104038	5	31	part_of	residues	853:860	arg1	HbCLP1	HbCLP1		residues		PUBTATOR	AminoAcid	HbCLP1	110639626	residues Glu117 and Glu147	Sequence alignments showed that in the two proteins the catalytic residues Glu117 and Glu147 in HbCLP1 and HbCLP2, respectively, were mutated to Ala, accounting for the lack of activity.
28620376	0	35	gly	N-Glycosylation	4:18	arg1	Mouse Immunoglobulin G	Mouse Immunoglobulin G				PUBTATOR		Mouse Immunoglobulin G	668542		The N-Glycosylation of Mouse Immunoglobulin G (IgG)-Fragment Crystallizable Differs Between IgG Subclasses and Strains.
28620376	0	35	gly	N-Glycosylation	4:18	arg1	IgG	IgG				PUBTATOR		IgG	668542		The N-Glycosylation of Mouse Immunoglobulin G (IgG)-Fragment Crystallizable Differs Between IgG Subclasses and Strains.