Literature DB >> 3794716

Deuterium isotope effect in gamma-aminobutyric acid transamination: determination of rate-limiting step.

P H Yu, D A Durden, B A Davis, A A Boulton.   

Abstract

The rate of transamination of gamma-aminobutryic acid (GABA) catalyzed by hog brain gamma-aminobutyrate aminotransferase was substantially reduced when the hydrogen at the gamma-carbon position was replaced by deuterium. The deuterium isotope effect of this reaction has been substantiated by fluorometric, radiometric, and mass spectrometric procedures and assessed kinetically. The ratios of Vmax of the nonlabeled substrate/Vmax of the deuterated substrate obtained under different conditions ranged from 6 to 7. This indicates that the cleavage of the hydrogen from the gamma-carbon is the rate-determining step in GABA transamination. Similar isotope effects have also been shown to occur in the peripheral system in vivo.

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Year:  1987        PMID: 3794716     DOI: 10.1111/j.1471-4159.1987.tb04112.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  3 in total

1.  Active site model for gamma-aminobutyrate aminotransferase explains substrate specificity and inhibitor reactivities.

Authors:  M D Toney; S Pascarella; D De Biase
Journal:  Protein Sci       Date:  1995-11       Impact factor: 6.725

2.  Synthesis and evaluation of novel heteroaromatic substrates of GABA aminotransferase.

Authors:  Dustin D Hawker; Richard B Silverman
Journal:  Bioorg Med Chem       Date:  2012-08-16       Impact factor: 3.641

3.  Theoretical and Mechanistic Validation of Global Kinetic Parameters of the Inactivation of GABA Aminotransferase by OV329 and CPP-115.

Authors:  Pathum M Weerawarna; Matthew J Moschitto; Richard B Silverman
Journal:  ACS Chem Biol       Date:  2021-03-18       Impact factor: 5.100

  3 in total

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