Free energy calculations of A2A adenosine receptor mutation effects on agonist binding†
Abstract
A general computational scheme to evaluate the effects of single point mutations on ligand binding is reported. This scheme is applied to characterize agonist binding to the A2A adenosine receptor, and is found to accurately explain how point mutations of different nature affect the binding affinity of a potent agonist.
- This article is part of the themed collection: Identification and Optimization of GPCR Ligands in the 21st Century