GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000041
Gene Ontology annotation based on UniPathway vocabulary mapping
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
GO_REF:0000108
Automatic assignment of GO terms using logical inference, based on on inter-ontology links
GO_REF:0000117
Electronic Gene Ontology annotations created by ARBA machine learning models
PMID:23122588
Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease.
PMID:30030519
Structure of the intact 14-subunit human cytochrome c oxidase.
PMID:32296183
A reference map of the human binary protein interactome.
PMID:34800366
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.
PMID:8382530
Isolation of a cDNA specifying subunit VIIb of human cytochrome c oxidase.
Reactome:R-HSA-163214
Electron transfer from reduced cytochrome c to molecular oxygen
Reactome:R-HSA-9709406
CO binds to Cytochrome c oxidase
Reactome:R-HSA-9865579
MT-CO1 and MT-CO2 complexes associate, installing heme moieties
Reactome:R-HSA-9865663
MT-CO3, COX6A,B,7A and NDUFA4 bind to holo-MT-CO1,2 complex
file:human/COX7B/COX7B-uniprot.txt
UniProtKB entry P24311 (COX7B_HUMAN)