| Literature DB >> 28965398 |
Haohao Fu1, Wensheng Cai1,2, Jérôme Hénin3, Benoît Roux4,5, Christophe Chipot6,7,8.
Abstract
To improve sampling of the configurational entropy change upon protein-ligand binding, we have introduced a new set of coarse variables describing the relative orientation and position of the ligand via a global macromolecular orientational procedure, onto which geometrical restraints are applied. Evaluating the potential of mean force for the different coarse variables, the experimental standard binding free energy for three decapeptides associated with the SH3 domain of the Abl kinase is reproduced quantitatively.Mesh:
Substances:
Year: 2017 PMID: 28965398 DOI: 10.1021/acs.jctc.7b00791
Source DB: PubMed Journal: J Chem Theory Comput ISSN: 1549-9618 Impact factor: 6.006