6vlt
Crystal Structure of Human P450 2C9*2 Genetic Variant in Complex with Losartan
Structural highlights
Publication Abstract from PubMedThe human cytochrome P450 2C9 (CYP2C9) plays a crucial role in the metabolic clearance of a wide range of clinical therapeutics. The *2 allele is a prevalent genetic variation in CYP2C9 that is found in various populations. A marked reduction of catalytic activity towards many important drug substrates has been demonstrated by CYP2C9*2, which represents an amino acid variation at position 144 from arginine to cysteine. The crystal structure of CYP2C9*2 in complex with an anti-hypertensive drug losartan was solved using X-ray crystallography at 3.1 A resolution. The Arg144Cys variation in the *2 complex disrupts the hydrogen bonding interactions that were observed between the side chain of arginine and neighboring residues in the losartan complex of CYP2C9 and the wild-type (WT) ligand-free structure. The conformation of several secondary structural elements is affected, thereby altering the binding and orientation of drug and important amino acid side chains in the distal active site cavity. The new structure revealed distinct interactions of losartan in the compact active site of CYP2C9*2 and differed in occupancy at the other binding sites previously identified in the WT-losartan complex. Furthermore, the binding studies in solution using losartan illustrated lower activity of the CYP2C9*2 compared to the WT. Together, the findings yield valuable insights into the decreased hydroxylation activity of losartan in patients carrying CYP2C9*2 allele, and provide a useful framework to investigate the effect of a single nucleotide polymorphism that leads to altered metabolism of diverse drug substrates. Significance Statement The *2 allele of the human drug metabolizing enzyme CYP2C9 is found in different populations and results in significantly reduced activity towards various drug substrates. How the CYP2C9*2 variant induces altered drug metabolism is poorly understood given that the Arg144Cys variation is located far away from the active site. This work yield insight into the effect of distal variation using multitude of techniques that include X-ray crystallography, isothermal titration calorimetry, enzymatic characterization and computational studies. Structure of cytochrome P450 2C9*2 in complex with an anti-hypertensive drug losartan: Insights into the effect of genetic polymorphism.,Parikh SJ, Evans CM, Obi JO, Zhang Q, Maekawa K, Glass KC, Shah MB Mol Pharmacol. 2020 Sep 16. pii: molpharm.120.000042. doi:, 10.1124/molpharm.120.000042. PMID:32938720[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
| ||||||||||||||||||||
