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V-type proton ATPase subunit S1
Summary
- UniProt ID
- Q15904
- Gene Symbol
-
- ATP6AP1
- ATP6IP1
- ATP6S1
- VATPS1
- XAP3
- Organism
- Homo sapiens (human)
External Links
- GlycoProtDB
- GPDB0011941
- GlyConnect
- GlyGen
- Q15904
- PubChem
- Q15904
- The Human Metabolome Database
- HMDBP09536
- The O-GlcNAc Database
- Q15904
- RaftProt
- Q15904
- O-GlcNAcAtlas
- Q15904
Annotation
- Keyword
-
- 3D-structure
- Congenital disorder of glycosylation
- Cytoplasmic vesicle
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Glycoprotein
- Hydrogen ion transport
- Phosphoprotein
- Reference proteome
- Signal
- Synapse
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| clathrin-coated vesicle membrane |
| endoplasmic reticulum-Golgi intermediate compartment membrane |
| GO Term |
|---|
| transporter activator activity |
| ATPase activator activity |
| small GTPase binding |
Sequence
MMAAMATARVRMGPRCAQALWRMPWLPVFLSLAAAAAAAAAEQQVPLVLWSSDRDLWAPAADTHEGHITSDLQLSTYLDPALELGPRNVLLFLQDKLSIEDFTAYGGVFGNKQDSAFSNLENALDLAPSSLVLPAVDWYAVSTLTTYLQEKLGASPLHVDLATLRELKLNASLPALLLIRLPYTASSGLMAPREVLTGNDEVIGQVLSTLKSEDVPYTAALTAVRPSRVARDVAVVAGGLGRQLLQKQPVSPVIHPPVSYNDTAPRILFWAQNFSVAYKDQWEDLTPLTFGVQELNLTGSFWNDSFARLSLTYERLFGTTVTFKFILANRLYPVSARHWFTMERLEVHSNGSVAYFNASQVTGPSIYSFHCEYVSSLSKKGSLLVARTQPSPWQMMLQDFQIQAFNVMGEQFSYASDCASFFSPGIWMGLLTSLFMLFIFTYGLHMILSLKTMDRFDDHKGPTISLTQIV
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Insulin receptor recycling | Homo sapiens |
| Ion channel transport | Homo sapiens |
| RHOA GTPase cycle | Homo sapiens |
| Transferrin endocytosis and recycling | 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:0050429 | Hailey-Hailey disease | |
| DOID:0050873 | follicular lymphoma | |
| DOID:0060262 | gallbladder disease | |
| DOID:0060762 | restrictive dermopathy | |
| DOID:0060862 | mal de Meleda | |
| DOID:0070129 | autosomal recessive cutis laxa type IID | |
| DOID:0070130 | autosomal dominant cutis laxa 1 | |
| DOID:0070131 | autosomal dominant cutis laxa 3 | |
| DOID:0070132 | autosomal recessive cutis laxa type IIIA | |
| DOID:0070133 | autosomal recessive cutis laxa type IB |
