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. 1993 Oct 11;332(1-2):35-6.
doi: 10.1016/0014-5793(93)80477-c.

Kinetic analysis on the substrate specificity of 3-isopropylmalate dehydrogenase

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Free article

Kinetic analysis on the substrate specificity of 3-isopropylmalate dehydrogenase

K Miyazaki et al. FEBS Lett. .
Free article

Abstract

Substrate specificity of 3-isopropylmalate dehydrogenase is analyzed using a series of synthetic (2R,3S)-3-alkylmalates. Each analog with hydrogen, methyl, ethyl, isopropyl, isobutyl, tert-butyl, and isoamyl group on C-3 functions as a substrate, implying a broad substrate specificity of the enzyme toward alkylmalates. The incremental binding energy of the isopropyl group of 3-isopropylmalate to the enzyme is estimated to be 3.55 kcal/mol, the rather small value supporting the broad specificity. Although the enzyme shows a broad specificity toward the alkylmalates, it does not show activity with isocitrate which has a negatively charged carboxymethyl group instead of the alkyl groups.

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