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ATPase H+ transporting V1 subunit E1
Summary
- Gene Symbol
-
- ATP6V1E1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Cell membrane
- Cytoplasmic vesicle
- Direct protein sequencing
- Disease variant
- Hydrogen ion transport
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Synapse
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| regulation of macroautophagy | ||
| synaptic vesicle lumen acidification | ||
| proton transmembrane transport |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| proton-transporting ATPase activity, rotational mechanism | ||
| ATPase binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- transporter
- Functional Category
-
- C: Energy production and conversion
- D: Cell cycle control, cell division, chromosome partitioning
- P: Inorganic ion transport and metabolism
| Gene Ontology |
|---|
| monoatomic ion transport |
| proton-transporting ATPase activity, rotational mechanism |
| InterPro |
|---|
| V-type ATPase subunit E, C-terminal domain superfamily |
| V-type ATPase subunit E |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070140 | autosomal recessive cutis laxa type IIC |
