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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Lactosylceramide alpha-2,3-sialyltransferase
Summary
- UniProt ID
- Q9UNP4
- Gene Symbol
-
- ST3GAL5
- SIAT9
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q9UNP4
- PubChem
- Q9UNP4
- SwissLipids
- The Human Metabolome Database
- HMDBP00772
Annotation
- Keyword
-
- Alternative splicing
- Disulfide bond
- Epilepsy
- Glycoprotein
- Glycosyltransferase
- Golgi apparatus
- Intellectual disability
- Lipid metabolism
- Reference proteome
- Signal-anchor
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| glycosphingolipid biosynthetic process |
| protein glycosylation |
| ganglioside biosynthetic process |
| GO Term |
|---|
| Golgi membrane |
| membrane |
| GO Term |
|---|
| sialyltransferase activity |
| lactosylceramide alpha-2,3-sialyltransferase activity |
| beta-galactoside (CMP) alpha-2,3-sialyltransferase activity |
Sequence
MRTKAAGCAERRPLQPRTEAAAAPAGRAMPSEYTYVKLRSDCSRPSLQWYTRAQSKMRRPSLLLKDILKCTLLVFGVWILYILKLNYTTEECDMKKMHYVDPDHVKRAQKYAQQVLQKECRPKFAKTSMALLFEHRYSVDLLPFVQKAPKDSEAESKYDPPFGFRKFSSKVQTLLELLPEHDLPEHLKAKTCRRCVVIGSGGILHGLELGHTLNQFDVVIRLNSAPVEGYSEHVGNKTTIRMTYPEGAPLSDLEYYSNDLFVAVLFKSVDFNWLQAMVKKETLPFWVRLFFWKQVAEKIPLQPKHFRILNPVIIKETAFDILQYSEPQSRFWGRDKNVPTIGVIAVVLATHLCDEVSLAGFGYDLNQPRTPLHYFDSQCMAAMNFQTMHNVTTETKFLLKLVKEGVVKDLSGGIDREF
Glycosylation Sites
G83460ZZ
G62765YT
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Glycosphingolipid biosynthesis | Homo sapiens |
| Sialic acid metabolism | 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:0050841 | focal hand dystonia | |
| DOID:0050886 | Troyer syndrome | |
| DOID:0060245 | Mast syndrome | |
| DOID:0060246 | MASA syndrome | |
| DOID:0060470 | salt and pepper syndrome | |
| DOID:0060491 | SPOAN syndrome | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0070113 | Niemann-Pick disease type C1 | |
| DOID:0080067 | Charcot-Marie-Tooth disease type 5 | |
| DOID:0080470 | developmental and epileptic encephalopathy 36 |
