Journal of Biological Chemistry · 2015 · 38 citations · 18 references
Life SciencesBiochemistryMolecular BiologyEnzymologyMetabolismStructural BiologyCatalytic MechanismsEnzyme CharacterizationEnzyme FunctionEnzyme StructureProtein ChemistryProtein StructureDecarboxylase EnzymesEnzyme Function AnnotationEnzyme Function ClassificationEnzyme Structure-function RelationshipsMicrobial Enzyme FunctionMulti-domain ProteinsProtein Function RelationshipsProtein Structure-function Analysis
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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Johannes Schindelin, Ignacio Arganda‐Carreras, Erwin Frise et al. · Nature Methods · 2012 · 70.9K citations
Crystal structure and mechanism of a carbon–carbon bond hydrolase
David E. Timm, H.A. Mueller, P. Bhanumoorthy et al. · Structure · 1999 · 81 citations