Role of the active-site solvent in the thermodynamics of factor Xa ligand binding.

ABSTRACT: Understanding the underlying physics of the binding of small-molecule ligands to protein active sites is a key objective of computational chemistry and biology. It is widely believed that displacement of water molecules from the active site by the ligand is a principal (if not the dominant) source of binding free energy. Although continuum theories of hydration are routinely used to describe the contributions of the solvent to the binding affinity of the complex, it is still an unsettled question as to whether or not these continuum solvation theories describe the underlying molecular physics with sufficient accuracy to reliably rank the binding affinities of a set of ligands for a given protein. Here we develop a novel, computationally efficient descriptor of the contribution of the solve

SUBMITTER: Abel R 

PROVIDER: S-EPMC2761766 | biostudies-literature | 2008 Mar

REPOSITORIES: biostudies-literature