Differential Catalytic Efficiency and Enantioselectivity of Murine GlutathioneS-Transferase Isoenzymes in the Glutathione Conjugation of CarcinogenicAnti-Diol Epoxides of Chrysene and Benzo(g)chrysene
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics
Reference31 articles.
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1. Specificity of Glutathione S-Transferases in the Glutathione Conjugation of Carcinogenic Diol Epoxides;Toxicology of Glutathione Transferases;2006-07-27
2. Role of arginine 216 in catalytic activity of murine Alpha class glutathione transferases mGSTAl-1 and mGSTA2-2 toward carcinogenic diol epoxides of polycyclic aromatic hydrocarbons;Carcinogenesis;2001-08-01
3. Specificity of murine glutathione S- transferase isozymes in the glutathione conjugation of (–)- anti- and (+)-syn-stereoisomers of benzo[g]chrysene 11,12-diol 13,14-epoxide;Carcinogenesis;1999-10
4. Detoxification of optically active bay- and fjord-region polycyclic aromatic hydrocarbon dihydrodiol epoxides by human glutathione transferase P1-1 expressed in Chinese hamster V79 cells;Carcinogenesis;1998-11-01
5. Cloning, Expression, and Biochemical Characterization of a Functionally Novel Alpha Class GlutathioneS-Transferase with Exceptional Activity in the Glutathione Conjugation of (+)-Anti-7,8-dihydroxy-9,10-oxy-7,8,9,10-tetrahydrobenzo(a)pyrene;Archives of Biochemistry and Biophysics;1998-05
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