AbstractKidney cysteine conjugate β-lyase (glutamine transaminase K, kyneurenine aminotransferase, EC 2.6.1.64) metabolises the cysteine conjugates of certain halogenated alkenes and alkanes to form reactive metabolites which can produce nephrotoxicicity and neurotoxicicity in experimental animals and man. Using a combination of hybridisation screening and PCR techniques we have isolated a full-length cDNA for human kidney cysteine conjugate β-lyase. Comparison of the deduced amino acid sequence with that of the rat enzyme indicated an 82% overall similarity, with 90% similarity around the pyridoxal phosphate binding site, many of the changes being conservative in nature. Expression of the cDNA in Cos-1 cells resulted in the production of a...
To better understand species differences in cisplatin nephrotoxicity, we focused on renal cysteine-S...
AbstractThe enzyme kynurenine aminotransferase (KAT) catalyses the conversion of l-kynurenine to kyn...
SIGLEAvailable from British Library Document Supply Centre- DSC:DX180468 / BLDSC - British Library D...
AbstractKidney cysteine conjugate β-lyase (glutamine transaminase K, kyneurenine aminotransferase, E...
A major route of detoxification for many halogenated xenobiotics is by conjugation to the tripeptide...
Many halogenated xenobiotics such as the environmental contaminant trichloroethylene are detoxified ...
The mercapturic acid pathway is an important detoxication mechanism in mammalian cells/tissues. Howe...
The role of rat kidney cysteine conjugate $-Iyase in the produc-tion of nephrotoic thiols from S-cys...
Rat kidney glutamine transaminase K (GTK) exhibits broad specificity both as an aminotransferase and...
Rat kidney glutamine transaminase K (GTK) exhibits broad specificity both as an aminotransferase and...
Cysteine conjugate β-lyase (β-lyase) was purified to electrophoretic homogeneity from the kidney cyt...
AbstractBackgroundKynurenine aminotransferase 3 (KAT3) catalyzes the transamination of Kynurenine to...
We have recently cloned, sequenced, and characterized a rat kidney cDNA (D2) that stimulates cystine...
Cysteine S-conjugate β-lyases are pyridoxal 5\u27-phosphate-containing enzymes that catalyze β-elimi...
SIGLEAvailable from British Library Document Supply Centre- DSC:DX185597 / BLDSC - British Library D...
To better understand species differences in cisplatin nephrotoxicity, we focused on renal cysteine-S...
AbstractThe enzyme kynurenine aminotransferase (KAT) catalyses the conversion of l-kynurenine to kyn...
SIGLEAvailable from British Library Document Supply Centre- DSC:DX180468 / BLDSC - British Library D...
AbstractKidney cysteine conjugate β-lyase (glutamine transaminase K, kyneurenine aminotransferase, E...
A major route of detoxification for many halogenated xenobiotics is by conjugation to the tripeptide...
Many halogenated xenobiotics such as the environmental contaminant trichloroethylene are detoxified ...
The mercapturic acid pathway is an important detoxication mechanism in mammalian cells/tissues. Howe...
The role of rat kidney cysteine conjugate $-Iyase in the produc-tion of nephrotoic thiols from S-cys...
Rat kidney glutamine transaminase K (GTK) exhibits broad specificity both as an aminotransferase and...
Rat kidney glutamine transaminase K (GTK) exhibits broad specificity both as an aminotransferase and...
Cysteine conjugate β-lyase (β-lyase) was purified to electrophoretic homogeneity from the kidney cyt...
AbstractBackgroundKynurenine aminotransferase 3 (KAT3) catalyzes the transamination of Kynurenine to...
We have recently cloned, sequenced, and characterized a rat kidney cDNA (D2) that stimulates cystine...
Cysteine S-conjugate β-lyases are pyridoxal 5\u27-phosphate-containing enzymes that catalyze β-elimi...
SIGLEAvailable from British Library Document Supply Centre- DSC:DX185597 / BLDSC - British Library D...
To better understand species differences in cisplatin nephrotoxicity, we focused on renal cysteine-S...
AbstractThe enzyme kynurenine aminotransferase (KAT) catalyses the conversion of l-kynurenine to kyn...
SIGLEAvailable from British Library Document Supply Centre- DSC:DX180468 / BLDSC - British Library D...