cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
Protohaem IX farnesyltransferase, mitochondria
UbiA prenyltransferase conserved site, protein family
protoheme IX farnesyltransferase activity
transferase activity, transferring alkyl or aryl (other than methyl) groups
Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant
Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency
Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency