کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1925811 | 1536418 | 2011 | 10 صفحه PDF | دانلود رایگان |

Cytochrome P450s (CYPs) are heme-containing monooxygenases that contribute to an enormous range of enzymatic function including biosynthetic and detoxification roles. This review summarizes recent studies concerning interactions of CYPs with ligands including substrates, inhibitors, and diatomic heme-ligating molecules. These studies highlight the complexity in the relationship between the heme spin state and active site occupancy, the roles of water in directing protein–ligand and ligand–heme interactions, and the details of interactions between heme and gaseous diatomic CYP ligands. Both kinetic and thermodynamic aspects of ligand binding are considered.
Research highlights
► Review of recent methods and results for CYP–ligand interactions.
► New methods.
► Summarizes the complex relationship between spin state and ligand binding.
Journal: Archives of Biochemistry and Biophysics - Volume 507, Issue 1, 1 March 2011, Pages 56–65