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A chemical model for the enzymatic mono de-alkylation of (methyl and ethyl) parathion by glutathione-S-transferase

✍ Scribed by Marie Dolores Maturano; Véronique Bongibault; Michèle Willson; Alain Klaébé; Didier Fournier


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
341 KB
Volume
53
Category
Article
ISSN
0040-4020

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✦ Synopsis


The NMR study of the reaction of methylparathion with thiol (glutathione) and a tertiary amine shows nnambiguously a sequential transfer of the methyl group firstly to the amine and secondly to the thiol. The reaction stops after a single demethylation. This observation may account for regiospecificity of some glutathione-S-transferases.