Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kevin D. McCarty"'
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 16, p 9020 (2024)
Cytochrome P450 (P450) enzymes dominate steroid metabolism. In general, the simple C-hydroxylation reactions are mechanistically straightforward and are generally agreed to involve a perferryl oxygen species (formally FeO3+). Several of the steroid t
Externí odkaz:
https://doaj.org/article/360b5c5b8f9b41ccb18e32215ad5370d
Publikováno v:
Medicinal Chemistry Research.
Autor:
Jeffrey Y Jian, Kevin D McCarty, Jo Ann W Byl, F Peter Guengerich, Keir C Neuman, Neil Osheroff
Publikováno v:
Nucleic Acids Res
To perform double-stranded DNA passage, type II topoisomerases generate a covalent enzyme-cleaved DNA complex (i.e. cleavage complex). Although this complex is a requisite enzyme intermediate, it is also intrinsically dangerous to genomic stability.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a00dba8a24a38260445f90e51df0603
https://europepmc.org/articles/PMC10164583/
https://europepmc.org/articles/PMC10164583/
Autor:
Kevin D. McCarty, Molly E. Sullivan, Yasuhiro Tateishi, Tatiana Y. Hargrove, Galina I. Lepesheva, F. Peter Guengerich
Publikováno v:
Journal of Biological Chemistry. :104841
Publikováno v:
Drug Metab Dispos
Cytochrome P450 2D6 (CYP2D6) is a major drug metabolizing enzyme with a buried active site. Channels leading to the active site from various enzyme surfaces are believed to facilitate ligand egress and access to the active site. The present study use
Publikováno v:
The Journal of Biological Chemistry
It has been recognized for >50 years that cytochrome b5 (b5) stimulates some cytochrome P450 (P450)–catalyzed oxidations, but the basis of this function is still not understood well. The strongest stimulation of catalytic activity by b5 is in the P
Publikováno v:
The Journal of Biological Chemistry
Cytochrome P450 (P450) 3A4 is the enzyme most involved in the metabolism of drugs and can also oxidize numerous steroids. This enzyme is also involved in one-half of pharmacokinetic drug–drug interactions, but details of the exact mechanisms of P45
Publikováno v:
The Journal of Biological Chemistry
Cytochrome P450 (P450) 17A1 catalyzes the 17α-hydroxylation of progesterone and pregnenolone as well as the subsequent lyase cleavage of both products to generate androgens. However, the selective inhibition of the lyase reactions, particularly with
Publikováno v:
The FASEB Journal. 34:1-1