Mutations in myosin S2 alter cardiac myosin-binding protein-C interaction in hypertrophic cardiomyopathy in a phosphorylation-dependent manner

Hypertrophic cardiomyopathy (HCM) is an inherited cardiovascular disorder primarily caused by mutations in the β-myosin heavy-chain gene. The proximal subfragment 2 region (S2), 126 amino acids of myosin, binds with the C0-C2 region of cardiac myosin-binding protein-C to regulate cardiac muscle cont...

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Detalles Bibliográficos
Autores principales: Singh, Rohit R., McNamara, James W., Sadayappan, Sakthivel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8239744/
https://www.ncbi.nlm.nih.gov/pubmed/34051236
http://dx.doi.org/10.1016/j.jbc.2021.100836

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8239744/
https://www.ncbi.nlm.nih.gov/pubmed/34051236
http://dx.doi.org/10.1016/j.jbc.2021.100836

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