9TPJ image
Deposition Date 2025-12-18
Release Date 2026-06-17
Last Version Date 2026-06-17
Entry Detail
PDB ID:
9TPJ
Keywords:
Title:
Human Cardiac Interacting Heads Motif, E525K mutant
Biological Source:
Source Organism(s):
Homo sapiens (Taxon ID: 9606)
Expression System(s):
Method Details:
Experimental Method:
Resolution:
3.02 Å
Aggregation State:
PARTICLE
Reconstruction Method:
SINGLE PARTICLE
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Myosin-7
Gene (Uniprot):MYH7
Mutagens:E525K
Chain IDs:A, B
Chain Length:1935
Number of Molecules:2
Biological Source:Homo sapiens
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Myosin light chain 3
Gene (Uniprot):MYL3
Chain IDs:C, D
Chain Length:195
Number of Molecules:2
Biological Source:Homo sapiens
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Myosin regulatory light chain
Gene (Uniprot):MYL2
Chain IDs:E, F
Chain Length:166
Number of Molecules:2
Biological Source:Homo sapiens
Modified Residue
Compound ID Chain ID Parent Comp ID Details 2D Image
M3L A LYS modified residue
Primary Citation
Dynamics of the beta-cardiac myosin auto-inhibited state explain cardiomyopathy pathogenesis.
Nat Commun ? ? ? (2026)
PMID: 42243087 DOI: 10.1038/s41467-026-73572-5

Abstact

Cardiac contractility requires precise regulation. A recently discovered form of regulation of cardiac contractility involves a beta-cardiac myosin off-state, the Interacting-Heads Motif ((Car)IHM). Despite its central role in cardiac physiology and disease, (Car)IHM structural dynamics remain poorly understood. Here, we integrate near-atomic resolution cryo-EM with all-atom molecular dynamics to characterize (Car)IHM in solution and in the context of the filament. We describe its conformational ensembles maintained by dynamic interfaces, and the stabilizing effect of the dilated cardiomyopathy mutation E525K, which limits S2 coiled-coil flexibility and impairs myosin activation. Intrinsically disordered regions of (Car)IHM and MyBP-C further modulate these dynamics. Our findings provide evidence for how (Car)IHM ensembles balance off/on states and anchor myosin heads in distinct thick filament environments. This integrated structural and dynamic approach enhances the understanding of thick filament regulation and facilitates predictions of the effects of genetic variants in inherited cardiomyopathies.

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Protein

Chemical

Disease

Primary Citation of related structures
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