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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 4
Summary
- UniProt ID
- Q11206
- Gene Symbol
-
- ST3GAL4
- CGS23
- NANTA3
- SIAT4C
- STZ
- Organism
- Homo sapiens (human)
External Links
- GlycoProtDB
- GPDB0011826
- GlyGen
- Q11206
- PubChem
- Q11206
- SwissLipids
- The Human Metabolome Database
- HMDBP03118
- The O-GlcNAc Database
- Q11206
- O-GlcNAcAtlas
- Q11206
Annotation
- Keyword
-
- Alternative splicing
- Disulfide bond
- Glycoprotein
- Glycosyltransferase
- Golgi apparatus
- Lipid metabolism
- Reference proteome
- Secreted
- Signal-anchor
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| Golgi membrane |
| extracellular region |
| Golgi cisterna membrane |
| membrane |
Sequence
MVSKSRWKLLAMLALVLVVMVWYSISREDRYIELFYFPIPEKKEPCLQGEAESKASKLFGNYSRDQPIFLRLEDYFWVKTPSAYELPYGTKGSEDLLLRVLAITSSSIPKNIQSLRCRRCVVVGNGHRLRNSSLGDAINKYDVVIRLNNAPVAGYEGDVGSKTTMRLFYPESAHFDPKVENNPDTLLVLVAFKAMDFHWIETILSDKKRVRKGFWKQPPLIWDVNPKQIRILNPFFMEIAADKLLSLPMQQPRKIKQKPTTGLLAITLALHLCDLVHIAGFGYPDAYNKKQTIHYYEQITLKSMAGSGHNVSQEALAIKRMLEMGAIKNLTSF
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 61 | N-linked (GlcNAc...) asparagine | |||
| 131 | N-linked (GlcNAc...) asparagine | |||
| 132 |
|
|||
| 310 | N-linked (GlcNAc...) asparagine | |||
| 329 | N-linked (GlcNAc...) asparagine |
|
G83460ZZ
G80920RR
G49108TO
G46503DX
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Keratan sulfate biosynthesis | Homo sapiens |
| Lewis blood group biosynthesis | Homo sapiens |
| Maturation of protein 3a | Homo sapiens |
| Maturation of protein 3a | Homo sapiens |
| Maturation of spike protein | Homo sapiens |
| N-Glycan antennae elongation | Homo sapiens |
| Pre-NOTCH Processing in Golgi | Homo sapiens |
| Sialic acid metabolism | Homo sapiens |
| Termination of O-glycan biosynthesis | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | |
| DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | |
| DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | |
| DOID:0110281 | autosomal recessive limb-girdle muscular dystrophy type 2G | |
| DOID:0110282 | autosomal recessive limb-girdle muscular dystrophy type 2H | |
| DOID:0110283 | autosomal recessive limb-girdle muscular dystrophy type 2J | |
| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | |
| DOID:0110285 | autosomal recessive limb-girdle muscular dystrophy type 2Q | |
| DOID:0110286 | obsolete autosomal recessive limb-girdle muscular dystrophy type 2R | |
| DOID:0110287 | autosomal recessive limb-girdle muscular dystrophy type 2S |
