8g4l
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Cryo-EM structure of the human cardiac myosin filament
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Structural highlights
DiseaseMYL3_HUMAN Familial isolated hypertrophic cardiomyopathy. The disease is caused by mutations affecting the gene represented in this entry. FunctionMYL3_HUMAN Regulatory light chain of myosin. Does not bind calcium. Contents | ||||||||||||||||||
This page was last modified 13:07, 1 November 2023.