Cytochrome c oxidase subunit I: Difference between revisions

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[[Category:Genes on human chromosome 17]]
[[Category:Genes on human chromosome 17]]
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== Cytochrome c oxidase subunit I ==
<gallery>
File:PDB_1occ_EBI.jpg|PDB 1occ EBI
File:Map_of_the_human_mitochondrial_genome.svg|Map of the human mitochondrial genome
File:Colonic_crypts_within_four_tissue_sections.jpg|Colonic crypts within four tissue sections
</gallery>

Latest revision as of 00:55, 27 February 2025

Cytochrome c oxidase subunit I (COI or COX1) is a protein that in humans is encoded by the MT-CO1 gene. It is a subunit of the enzyme cytochrome c oxidase (complex IV), which is the last enzyme in the mitochondrial electron transport chain of mitochondria.

Function[edit]

COX1 is one of the three mitochondrial DNA (mtDNA)-encoded subunits of cytochrome c oxidase. Cytochrome c oxidase is the terminal enzyme of the mitochondrial respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1-3 form the functional core of the enzyme complex. COX1, the largest subunit, forms the mitochondrial proton channel, and its polypeptide folds into a transmembrane helix that forms the core of the proton pump.

Clinical significance[edit]

Mutations in the MT-CO1 gene are associated with a variety of human diseases, including Leber's hereditary optic neuropathy, mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), and myoclonic epilepsy with ragged-red fibers (MERRF).

See also[edit]

References[edit]

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External links[edit]

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Cytochrome c oxidase subunit I[edit]