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Structural and Mechanistic Similarities of 6-phosphogluconate and 3-hydroxyisobutyrate Dehydrogenases Reveal a New Enzyme Family, the 3-hydroxyacid Dehydrogenases

Overview
Journal FEBS Lett
Specialty Biochemistry
Date 1996 Jul 8
PMID 8766712
Citations 14
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Abstract

Rat 3-hydroxyisobutyrate dehydrogenase exhibits significant amino acid sequence homology with 6-phosphogluconate dehydrogenase, D-phenylserine dehydrogenase from Pseudomonas syringae, and a number of hypothetical proteins encoded by genes of microbial origin. Key residues previously proposed to have roles in substrate binding and catalysis in sheep 6-phosphogluconate dehydrogenase are highly conserved in this entire family of enzymes. Site-directed mutagenesis, chemical modification, and substrate specificity studies were used to compare possible mechanistic similarities of 3-hydroxyisobutyrate dehydrogenase with 6-phosphogluconate dehydrogenase. The data suggest that 3-hydroxyisobutyrate and 6-phosphogluconate dehydrogenases may comprise, in part, a previously unrecognized family of 3-hydroxyacid dehydrogenases.

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