Improved prediction of HIV-1 protease-inhibitor binding energies by molecular dynamics simulations.

ABSTRACT:

Background

The accurate prediction of enzyme-substrate interaction energies is one of the major challenges in computational biology. This study describes the improvement of protein-ligand binding energy prediction by incorporating protein flexibility through the use of molecular dynamics (MD) simulations.

Results

Docking experiments were undertaken using the program AutoDock for twenty-five HIV-1 protease-inhibitor complexes determined by x-ray crystallography. Protein-rigid docking without any dynamics produced a low correlation of 0.38 between the experimental and calculated binding energies. Correlations improved significantly for all time scales of MD simulations of the receptor-ligand complex. The highest correlation coefficient of 0.87 between the experimental and calc

SUBMITTER: Jenwitheesuk E 

PROVIDER: S-EPMC154089 | biostudies-literature | 2003 Apr

REPOSITORIES: biostudies-literature