COX10: Difference between revisions
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Latest revision as of 05:54, 17 March 2025
COX10 also known as Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 is a protein that in humans is encoded by the COX10 gene. It is involved in the final stages of the mitochondrial electron transport chain, specifically in the synthesis of heme A, a component of cytochrome c oxidase (COX).
Function[edit]
COX10 is a mitochondrial protein involved in the biosynthesis of heme A, a prosthetic group of cytochrome c oxidase (COX). COX is the terminal enzyme of the mitochondrial respiratory chain and is responsible for the transfer of electrons from cytochrome c to oxygen. COX10 catalyzes the conversion of protoheme IX (heme B) to heme O, the penultimate step in the biosynthesis of heme A.
Clinical significance[edit]
Mutations in the COX10 gene have been associated with mitochondrial complex IV deficiency, a disorder of the mitochondrial respiratory chain with heterogeneous clinical manifestations, ranging from isolated myopathy to severe multisystem disease affecting several tissues and organs.
Structure[edit]
The COX10 protein is a member of the heme A:farnesyltransferase family. It is a multi-pass membrane protein that is located in the inner mitochondrial membrane. The protein is predicted to have 8 transmembrane domains.
See also[edit]
References[edit]
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