Early-Onset Hypertrophic Cardiomyopathy Mutations Significantly Increase the Velocity, Force, and Actin-Activated ATPase Activity of Human β-Cardiac Myosin
Early-onset HCM mutations increase myosin biomechanical functions D239N shows a large increase in velocity as compared to wild-type myosin H251N lowers S1-S2 binding affinity, which may increase available active myosin heads