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
Biol Chem Hoppe Seyler, 1989 vol.370:661-672
SNFG,
Text,
Oxford
taxonomy (1)
protein (1)
source (1)
structure (2)
composition (2)
disease (1)
reference (1)
site (1)
peptide (0)
- Homo sapiens (Human)
Taxonomy
- Urine (UBERON_0001088)
Source
- O-Linked / Core 1 / NeuAc(a2-3)Gal(b1-3)[NeuAc(a2-6)]GalNAc
- O-Linked / Core 2 / NeuAc(a2-3)Gal(b1-4)GlcNAc(b1-6)[NeuAc(a2-3)Gal(b1-3)]GalNAc
Reported structure
- Hex:1 HexNAc:1 NeuAc:2 (avg mass : 965.8685 )
- Hex:2 HexNAc:2 NeuAc:2 (avg mass : 1331.2059 )
Composition
- Lysosomal storage disease (DOID:3211)
Disease
-
Urine glycopeptide / Homo sapiens
- Undefined site
Reported glycosite
Mass spectrometry observed peptide
-
- O-Linked / Core 1 (avg mass : 965.8685)
- Urine (UBERON_0001088)
- Lysosomal storage disease (DOID:3211)
-
Urine glycopeptide / Homo sapiens
- Undefined site
-
- O-Linked / Core 2 (avg mass : 1331.2059)
- Urine (UBERON_0001088)
- Lysosomal storage disease (DOID:3211)
-
Urine glycopeptide / Homo sapiens
- Undefined site
Source
Disease
Reported glycosite
Source
Disease
Reported glycosite
