COX10: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
 
CSV import
 
(One intermediate revision by the same user not shown)
Line 29: Line 29:


{{medicine-stub}}
{{medicine-stub}}
{{No image}}
__NOINDEX__

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]

<references group="" responsive="1"></references>


Stub icon
   This article is a medical stub. You can help WikiMD by expanding it!