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The arrhythmogenic N53I variant subtly changes the structure and dynamics in the calmodulin N-terminal domain, altering its interaction with the cardiac ryanodine receptor

Mutations in the genes encoding the highly conserved Ca(2+)-sensing protein calmodulin (CaM) cause severe cardiac arrhythmias, including catecholaminergic polymorphic ventricular tachycardia or long QT syndrome and sudden cardiac death. Most of the identified arrhythmogenic mutations reside in the C...

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Bibliografske podrobnosti
izdano v:J Biol Chem
Main Authors: Holt, Christian, Hamborg, Louise, Lau, Kelvin, Brohus, Malene, Sørensen, Anders Bundgaard, Larsen, Kamilla Taunsig, Sommer, Cordula, Van Petegem, Filip, Overgaard, Michael Toft, Wimmer, Reinhard
Format: Artigo
Jezik:Inglês
Izdano: American Society for Biochemistry and Molecular Biology 2020
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7261784/
https://ncbi.nlm.nih.gov/pubmed/32317284
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA120.013430
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