| Literature DB >> 25575590 |
Haymo Pircher1, Susanne von Grafenstein2, Thomas Diener1, Christina Metzger1, Eva Albertini1, Andrea Taferner1, Hermann Unterluggauer1, Christian Kramer2, Klaus R Liedl2, Pidder Jansen-Dürr3.
Abstract
Fumarylacetoacetate hydrolase (FAH) domain-containing proteins occur in both prokaryotes and eukaryotes, where they carry out diverse enzymatic reactions, probably related to structural differences in their respective FAH domains; however, the precise relationship between structure of the FAH domain and the associated enzyme function remains elusive. In mammals, three FAH domain-containing proteins, FAHD1, FAHD2A, and FAHD2B, are known; however, their enzymatic function, if any, remains to be demonstrated. In bacteria, oxaloacetate is subject to enzymatic decarboxylation; however, oxaloacetate decarboxylases (ODx) were so far not identified in eukaryotes. Based on molecular modeling and subsequent biochemical investigations, we identified FAHD1 as a eukaryotic ODx enzyme. The results presented here indicate that dedicated oxaloacetate decarboxylases exist in eukaryotes.Entities:
Keywords: Computer Modeling; Decarboxylase; Energy Metabolism; FAH Domain; FAHD1; Mitochondria; Oxaloacetate Decarboxylase; Pyruvate
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Year: 2015 PMID: 25575590 PMCID: PMC4358102 DOI: 10.1074/jbc.M114.609305
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157