Application of molecular modeling for prediction of substrate specificity in cytochrome P450 1A2 mutants.

ABSTRACT: Molecular dynamics (MD) simulations of 7-ethoxy- and 7-methoxyresorufin bound in the active site of cytochrome P450 (P450) 1A2 wild-type and various mutants were used to predict changes in substrate specificity of the mutants. A total of 26 multiple mutants representing all possible combinations of five key amino acid residues, which are different between P450 1A1 and 1A2, were examined. The resorufin substrates were docked in the active site of each enzyme in the productive binding orientation, and MD simulations were performed on the enzyme-substrate complex. Ensembles collected from MD trajectories were then scored on the basis of geometric parameters relating substrate position with respect to the activated oxoheme cofactor. The results showed a high correlation between the previous ex

SUBMITTER: Tu Y 

PROVIDER: S-EPMC2574645 | biostudies-literature | 2008 Nov

REPOSITORIES: biostudies-literature