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MIRAGE
Cytochrome c oxidase assembly protein COX11, mitochondrial
Summary
- UniProt ID
- Q9Y6N1
- Gene Symbol
-
- COX11
- Gene ID
- 1353
- Organism
- Homo sapiens (human)
External Links
- The Human Metabolome Database
- HMDBP08242
- The O-GlcNAc Database
- Q9Y6N1
- Re-Glyco
- Q9Y6N1
Annotation
- Keyword
-
- Alternative splicing
- Copper
- Disease variant
- Mitochondrion inner membrane
- Primary mitochondrial disease
- Reference proteome
- Transit peptide
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| mitochondrion |
| mitochondrial inner membrane |
| protein-containing complex |
| GO Term |
|---|
| ATP biosynthetic process |
| intracellular monoatomic cation homeostasis |
| GO Term |
|---|
| copper ion binding |
| electron transfer activity |
Sequence
MGGLWRPGWRCVPFCGWRWIHPGSPTRAAERVEPFLRPEWSGTGGAERGLRWLGTWKRCSLRARHPALQPPRRPKSSNPFTRAQEEERRRQNKTTLTYVAAVAVGMLGASYAAVPLYRLYCQTTGLGGSAVAGHASDKIENMVPVKDRIIKISFNADVHASLQWNFRPQQTEIYVVPGETALAFYRAKNPTDKPVIGISTYNIVPFEAGQYFNKIQCFCFEEQRLNPQEEVDMPVFFYIDPEFAEDPRMIKVDLITLSYTFFEAKEGHKLPVPGYN
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 81 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Complex IV assembly | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070485 | mitochondrial complex IV deficiency nuclear type 23 |
