Identification of FAH Domain-containing Protein 1 (FAHD1) as Oxaloacetate Decarboxylase

被引:30
|
作者
Pircher, Haymo [1 ,2 ]
von Grafenstein, Susanne [2 ,3 ]
Diener, Thomas [1 ,2 ]
Metzger, Christina [1 ,2 ]
Albertini, Eva [1 ,2 ]
Taferner, Andrea [1 ,2 ]
Unterluggauer, Hermann [1 ,2 ]
Kramer, Christian [2 ,3 ]
Liedl, Klaus R. [2 ,3 ]
Janesn-Duerr, Pidder [1 ,2 ]
机构
[1] Univ Innsbruck, Inst Biomed Aging Res, A-6020 Innsbruck, Austria
[2] Univ Innsbruck, Ctr Mol Biosci Innsbruck, A-6020 Innsbruck, Austria
[3] Univ Innsbruck, Inst Gen Inorgan & Theoret Chem, A-6020 Innsbruck, Austria
关键词
HUMAN FUMARYLACETOACETATE HYDROLASE; CRYSTAL-STRUCTURE; MECHANISM; PURIFICATION; ENZYMES;
D O I
10.1074/jbc.M114.609305
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:6755 / 6762
页数:8
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