Cytochrome c oxidase subunit I: Difference between revisions
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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]
<references />
External links[edit]
Cytochrome c oxidase subunit I[edit]
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PDB 1occ EBI
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Map of the human mitochondrial genome
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Colonic crypts within four tissue sections
