| Literature DB >> 31655790 |
Pradeepraj Durairaj1, Linbing Fan1, Sangeeta Shrestha Sharma1, Zhao Jie1, Matthias Bureik1.
Abstract
CYP20A1 is a well-conserved member of the human cytochrome P450 enzyme family for which no endogenous or xenobiotic substrate is known. We have recently shown that this enzyme has moderate activity towards two proluciferin probe substrates. In order to facilitate the search for physiological substrates we have tested nine additional proluciferins in this study and identified three such probe substrates that give much higher product yields. Using one of these probes, we demonstrate inhibition of CYP20A1 activity by 1-benzylimidazole, ketoconazole and letrozole. Finally, we show that the combination of two common single nucleotide polymorphisms (SNPs) of CYP20A1 leads to an enzyme (CYP20A1Leu97Phe346) with reduced activity.Entities:
Keywords: S. pombe; cytochrome P450; enzyme inhibition; fission yeast; single nucleotide polymorphism
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Year: 2020 PMID: 31655790 DOI: 10.1515/hsz-2019-0307
Source DB: PubMed Journal: Biol Chem ISSN: 1431-6730 Impact factor: 3.915