Calculating protein-ligand binding affinities with MMPBSA: Method and error analysis.

ABSTRACT: Molecular Mechanics Poisson-Boltzmann Surface Area (MMPBSA) methods have become widely adopted in estimating protein-ligand binding affinities due to their efficiency and high correlation with experiment. Here different computational alternatives were investigated to assess their impact to the agreement of MMPBSA calculations with experiment. Seven receptor families with both high-quality crystal structures and binding affinities were selected. First the performance of nonpolar solvation models was studied and it was found that the modern approach that separately models hydrophobic and dispersion interactions dramatically reduces RMSD's of computed relative binding affinities. The numerical setup of the Poisson-Boltzmann methods was analyzed next. The data shows that the impact of grid spa

SUBMITTER: Wang C 

PROVIDER: S-EPMC5018451 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature