A cluster of negative charges at the amino terminal tail of CFTR regulates ATP-dependent channel gating

1. The cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel is activated by protein kinase A (PKA) phosphorylation of its R domain and by ATP binding at its nucleotide-binding domains (NBDs). Here we investigated the functional role of a cluster of acidic residues in the amino...

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Detalhes bibliográficos
Main Authors: Fu, Jian, Ji, Hong-Long, Naren, Anjaparavanda P, Kirk, Kevin L
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2001
Assuntos:
Research Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2278861/
https://ncbi.nlm.nih.gov/pubmed/11600681
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-7793.2001.0459c.xd
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