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Glycosylation sites
Urine glycopeptide (Homo sapiens)
All glycosylation sites
SNFG
,
Text
,
Oxford
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Site
Core / Type
Cartoon
Composition
Biological associations
Undefined site
O-Linked / Core 1
Hex:1 HexNAc:1 NeuAc:2
taxonomy (1)
protein (1)
source (1)
structure (1)
composition (1)
disease (1)
reference (1)
site (1)
peptide (0)
Taxonomy
Homo sapiens (Human)
Protein
Urine glycopeptide / Homo sapiens
# Export GlyConnect protein list related to glycosylation_site_structure with id 17900000002641 null # id : 179 Urine glycopeptide Homo sapiens
Source
Urine
(UBERON_0001088)
Reported structure
O-Linked / Core 1 / NeuAc(a2-3)Gal(b1-3)[NeuAc(a2-6)]GalNAc
Composition
Hex:1 HexNAc:1 NeuAc:2 (avg mass : 965.8685 )
# Export GlyConnect composition list related to glycosylation_site_structure with id 17900000002641 Hex:1 HexNAc:1 NeuAc:2 # id : 461 / avg mass :965.8685
Disease
Lysosomal storage disease
(DOID:3211)
Reference
Isolation and structural characterization of sialic-acid-containing glycopeptides of the O-glycosidic type from the urine of two patients with an hereditary deficiency in alpha-N-acetylgalactosaminidase activity. (1989 - Linden H, Klein R, Egge H, Peter-Katalinic J, Dabrowski J, Schindler D)
/ Status : Reviewed
Reported glycosite
Urine glycopeptide / Homo sapiens
Undefined site
Mass spectrometry observed peptide
Undefined site
O-Linked / Core 2
Hex:2 HexNAc:2 NeuAc:2
taxonomy (1)
protein (1)
source (1)
structure (1)
composition (1)
disease (1)
reference (1)
site (1)
peptide (0)
Taxonomy
Homo sapiens (Human)
Protein
Urine glycopeptide / Homo sapiens
# Export GlyConnect protein list related to glycosylation_site_structure with id 17900000003423 null # id : 179 Urine glycopeptide Homo sapiens
Source
Urine
(UBERON_0001088)
Reported structure
O-Linked / Core 2 / NeuAc(a2-3)Gal(b1-4)GlcNAc(b1-6)[NeuAc(a2-3)Gal(b1-3)]GalNAc
Composition
Hex:2 HexNAc:2 NeuAc:2 (avg mass : 1331.2059 )
# Export GlyConnect composition list related to glycosylation_site_structure with id 17900000003423 Hex:2 HexNAc:2 NeuAc:2 # id : 172 / avg mass :1331.2059
Disease
Lysosomal storage disease
(DOID:3211)
Reference
Isolation and structural characterization of sialic-acid-containing glycopeptides of the O-glycosidic type from the urine of two patients with an hereditary deficiency in alpha-N-acetylgalactosaminidase activity. (1989 - Linden H, Klein R, Egge H, Peter-Katalinic J, Dabrowski J, Schindler D)
/ Status : Reviewed
Reported glycosite
Urine glycopeptide / Homo sapiens
Undefined site
Mass spectrometry observed peptide
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