Literature DB >> 7648206

Time-dependent inhibition of gamma-aminobutyric acid aminotransferase, by 3-hydroxybenzylhydrazine.

E S Lightcap1, M H Hopkins, G T Olson, R B Silverman.   

Abstract

gamma-Aminobutyric acid (GABA) aminotransferase is a pyridoxal 5'-phosphate (PLP)-dependent enzyme that catalyzes the conversion of GABA into succinic semialdehyde. Hydrazine analogues have long been known to act as inactivators of PLP-dependent enzymes, including GABA aminotransferase, however, no studies of the molecular mechanism of inactivation of PLP-dependent enzymes by hydrazines have been reported. 3-Hydroxybenzylhydrazine is shown to be a potent in vitro time-dependent inhibitor of pig brain GABA aminotransferase. UV-visible and 1H NMR studies, both with GABA aminotransferase and with PLP as a chemical model for the enzyme-catalyzed reaction, indicate that 3-hydroxybenzylhydrazine reacts both enzymatically and nonenzymatically to form the 3-hydroxybenzylhydrazone of PLP without tautomerization.

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Year:  1995        PMID: 7648206     DOI: 10.1016/0968-0896(95)00070-w

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  1 in total

1.  Inhibition of Mycobacterium tuberculosis transaminase BioA by aryl hydrazines and hydrazides.

Authors:  Ran Dai; Daniel J Wilson; Todd W Geders; Courtney C Aldrich; Barry C Finzel
Journal:  Chembiochem       Date:  2014-01-31       Impact factor: 3.164

  1 in total

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