Type 2 ryanodine receptor domain A contains a unique and dynamic α-helix that transitions to a ß-strand in a mutant linked with a heritable cardiomyopathy.
J Mol Biol
; 425(21): 4034-46, 2013 Nov 01.
Article
em En
| MEDLINE
| ID: mdl-23978697
Palavras-chave
ARVD2; CPVT; CSI; CSP; HS-loop; HSQC; NMR; NOE; TROSY; arrhythmogenic right ventricular dysplasia type 2; calcium channel; catecholaminergic polymorphic ventricular tachycardia; chemical shift index; chemical shift perturbation; cryo-EM; cryo-electron microscopy; crystallography; disease mutation; heteronuclear single quantum coherence; hot-spot loop; nuclear Overhauser enhancement; protein dynamics; transverse relaxation optimized spectroscopy
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Éxons
/
Canal de Liberação de Cálcio do Receptor de Rianodina
/
Mutação
/
Cardiomiopatias
Limite:
Animals
Idioma:
En
Ano de publicação:
2013
Tipo de documento:
Article