Literature DB >> 8405445

Kinetic analysis on the substrate specificity of 3-isopropylmalate dehydrogenase.

K Miyazaki1, K Kakinuma, H Terasawa, T Oshima.   

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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Year:  1993        PMID: 8405445     DOI: 10.1016/0014-5793(93)80477-c

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  6 in total

1.  Molecular and phylogenetic characterization of isopropylmalate dehydrogenase of a thermoacidophilic archaeon, Sulfolobus sp. strain 7.

Authors:  T Suzuki; Y Inoki; A Yamagishi; T Iwasaki; T Wakagi; T Oshima
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

2.  Evolution of a transition state: role of Lys100 in the active site of isocitrate dehydrogenase.

Authors:  Stephen P Miller; Susana Gonçalves; Pedro M Matias; Antony M Dean
Journal:  Chembiochem       Date:  2014-05-02       Impact factor: 3.164

3.  A synthetic recursive "+1" pathway for carbon chain elongation.

Authors:  Ryan J Marcheschi; Han Li; Kechun Zhang; Elizabeth L Noey; Seonah Kim; Asha Chaubey; K N Houk; James C Liao
Journal:  ACS Chem Biol       Date:  2012-02-03       Impact factor: 5.100

4.  Modeling substrate binding in Thermus thermophilus isopropylmalate dehydrogenase.

Authors:  T Zhang; D E Koshland
Journal:  Protein Sci       Date:  1995-01       Impact factor: 6.725

5.  Escherichia coli D-malate dehydrogenase, a generalist enzyme active in the leucine biosynthesis pathway.

Authors:  Anastassia A Vorobieva; Mohammad Shahneawz Khan; Patrice Soumillion
Journal:  J Biol Chem       Date:  2014-08-26       Impact factor: 5.157

6.  The role of glutamate 87 in the kinetic mechanism of Thermus thermophilus isopropylmalate dehydrogenase.

Authors:  A M Dean; L Dvorak
Journal:  Protein Sci       Date:  1995-10       Impact factor: 6.725

  6 in total

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