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Hypertrophic cardiomyopathy mutations Y115H and E497D disrupt the folded-back state of human beta-cardiac myosin allosterically

2024-03-03

Abstract excerpt

At the molecular level, clinical hypercontractility associated with many hypertrophic cardiomyopathy (HCM)-causing mutations in beta-cardiac myosin appears to be driven by their disruptive effect on the energy-conserving, folded-back, super relaxed (SRX) OFF-state of myosin. A pathological increase in force production results from release of heads from this OFF-state, which results in an increase in the number of...

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Literature Corpus work
3dc86063-0fad-5690-82de-dc149f51f4a7
DOI
10.1101/2024.02.29.582851
Open publication

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Hypertrophic cardiomyopathy mutations Y115H and E497D disrupt the folded-back state of human beta-cardiac myosin allostericallyDOI 10.1101/2024.02.29.582851
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