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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.
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页码:6755 / 6762
页数:8
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