| Literature DB >> 22902835 |
Eduardo Balsa1, Ricardo Marco, Ester Perales-Clemente, Radek Szklarczyk, Enrique Calvo, Manuel O Landázuri, José Antonio Enríquez.
Abstract
The oxidative phosphorylation system is one of the best-characterized metabolic pathways. In mammals, the protein components and X-ray structures are defined for all complexes except complex I. Here, we show that NDUFA4, formerly considered a constituent of NADH Dehydrogenase (CI), is instead a component of the cytochrome c oxidase (CIV). Deletion of NDUFA4 does not perturb CI. Rather, proteomic, genetic, evolutionary, and biochemical analyses reveal that NDUFA4 plays a role in CIV function and biogenesis. The change in the attribution of the NDUFA4 protein requires renaming of the gene and reconsideration of the structure of CIV. Furthermore, NDUFA4 should be considered a candidate gene for CIV rather than CI deficiencies in humans.Entities:
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Year: 2012 PMID: 22902835 DOI: 10.1016/j.cmet.2012.07.015
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287