COX17
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Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). Cytochrome c oxidase copper chaperone is a protein that in humans is encoded by the COX17 gene.[1][2]
Function
Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be involved in the recruitment of copper to mitochondria for incorporation into the COX apoenzyme. This protein shares 92% amino acid sequence identity with mouse and rat Cox17 proteins. This gene is no longer considered to be a candidate gene for COX deficiency. A pseudogene COX17P has been found on chromosome 13.[2]
References
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External links
- COX17 human gene location in the UCSC Genome Browser.
- COX17 human gene details in the UCSC Genome Browser.
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