The molecular basis of hypercontractility caused by the hypertrophic cardiomyopathy mutations R403Q and R663H
S. S. Sarkar, D. V. Trivedi, M. M. Morck, A. S. Adhikari, S. N. Pasha, K. M. Ruppel, J. A. Spudich
This study investigates how HCM mutations R403Q and R663H in myosin cause hypercontractility by increasing functionally-accessible myosin heads and affecting MyBP-C binding.
bioRxiv · Feb 7, 2019 · PreprintBiochemistry