Biophysical properties of human β-cardiac myosin with converter mutations that cause hypertrophic cardiomyopathy
NIH| Molecular characterization of cardiomyopathy mutations in human cardiac myosin ,
NIH| Biomechanical analysis of converter domain mutations in human beta-cardiac myosin ,
NIH| Myosin Movement in Vitro - Molecular Characterization
Authors: Masataka Kawana; Saswata S. Sarkar; Shirley Sutton; Kathleen M. Ruppel; James A. Spudich;
Biophysical properties of human β-cardiac myosin with converter mutations that cause hypertrophic cardiomyopathy
Abstract
Converter HCM mutations cause only small changes in the biophysics of myosin, suggesting an alternative mechanism for hypercontractility.
Related Organizations
- Stanford University United States
- Stanford University School of Medicine United States
- Department of Biochemistry Stanford University School of Medicine United States
Keywords
Ventricular Myosins, Amino Acid Substitution, Genetic Diseases, Inborn, Mutation, Missense, Humans, Cardiomegaly, Research Articles
Ventricular Myosins, Amino Acid Substitution, Genetic Diseases, Inborn, Mutation, Missense, Humans, Cardiomegaly, Research Articles
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