Literature DB >> 22474332

SdhE is a conserved protein required for flavinylation of succinate dehydrogenase in bacteria.

Matthew B McNeil1, James S Clulow, Nabil M Wilf, George P C Salmond, Peter C Fineran.   

Abstract

Conserved uncharacterized genes account for ~30% of genes in both eukaryotic and bacterial genomes and are predicted to encode what are often termed "conserved hypothetical proteins." Many of these proteins have a wide phylogenetic distribution and might play important roles in conserved cellular pathways. Using the bacterium Serratia as a model system, we have investigated two conserved uncharacterized proteins, YgfY (a DUF339 protein, renamed SdhE; succinate dehydrogenase protein E) and YgfX (a DUF1434 protein). SdhE was required for growth on succinate as a sole carbon source and for the function, but not stability, of succinate dehydrogenase, an important component of the electron transport chain and the tricarboxylic acid cycle. SdhE interacted with the flavoprotein SdhA, directly bound the flavin adenine dinucleotide co-factor, and was required for the flavinylation of SdhA. This is the first demonstration of a protein required for FAD incorporation in bacteria. Furthermore, the loss of SdhE was highly pleiotropic, suggesting that SdhE might flavinylate other flavoproteins. Our findings are of wide importance to central metabolism because SdhE homologues are present in α-, β-, and γ-proteobacteria and multiple eukaryotes, including humans and yeast.

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Year:  2012        PMID: 22474332      PMCID: PMC3365757          DOI: 10.1074/jbc.M111.293803

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  45 in total

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  30 in total

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Review 5.  Catalytic mechanisms of complex II enzymes: a structural perspective.

Authors:  T M Iverson
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Review 6.  Structural basis for malfunction in complex II.

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