Article
Tail Length and E525K Dilated Cardiomyopathy Mutant Alter Human β-Cardiac Myosin Super-Relaxed State
2023-12-08
Abstract excerpt
Dilated cardiomyopathy (DCM) is characterized by impaired cardiac function due to myocardial hypo-contractility and is associated with point mutations in β-cardiac myosin, the molecular motor that powers cardiac contraction. Myocardial function can be modulated through sequestration of myosin motors into an auto-inhibited "super relaxed" state (SRX), which is further stabilized by a structural state known as the "...
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Identifiers and source
- Literature Corpus work
- d7c5c43b-86ab-59ee-840b-00546a261247
- DOI
- 10.1101/2023.12.07.570656
