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PMID: 6375677 Published · ppublish English Journal Article

Stereochemistry of the inactivation of 4-aminobutyrate: 2-oxoglutarate aminotransferase and L-glutamate 1-carboxylase by 4-aminohex-5-ynoic acid enantiomers.

Biochemical pharmacology ·Vol. 33 ·No. 11 ·1984-06-01 ·Pages 1741-6

Danzin C, Claverie N, Jung MJ

Abstract

Incubation of rat brain or bacterial 4-aminobutyrate aminotransferase (EC 2.6.1.19) with both (S)-(+)- and (R)-(-)-enantiomers of 4- aminohex -5- ynoic acid results in a time-dependent irreversible loss of enzymatic activity. Rat brain glutamate decarboxylase (EC 4.1.1.15) is inactivated by the (S)-(+)-enantiomer while the bacterial glutamate decarboxylase is inactivated by the (R)-(-)-enantiomer. In addition, we demonstrate that (R)-(-)-4- aminohex -5- ynoic acid is a selective and effective inhibitor of rat brain 4-aminobutyrate aminotransferase in vivo.

MeSH Terms
4-Aminobutyrate Transaminase/antagonists & inhibitors Alkynes Aminocaproates/pharmacology Animals Brain/enzymology Escherichia coli/enzymology Glutamate Decarboxylase/antagonists & inhibitors Rats Stereoisomerism Time Factors
Chemicals
Alkynes Aminocaproates 4-amino-5-hexynoic acid 4-Aminobutyrate Transaminase Glutamate Decarboxylase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Danzin C
Claverie N
Jung M J
Article Info
Journal
Biochemical pharmacology
Abbr.
Biochem Pharmacol
ISSN
0006-2952
Published
1984-06-01
Pages
1741-6
Language
English
Region
England
NLM ID
0101032
Subset
IM
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