Regulation of cystic fibrosis transmembrane conductance regulator single-channel gating by bivalent PDZ-domain-mediated interaction

The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-dependent protein kinase- and ATP-regulated chloride channel, the activity of which determines the rate of electrolyte and fluid transport in a variety of epithelial tissues. Here we describe a mechanism that regulates CFTR cha...

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Cyhoeddwyd yn:	Proc Natl Acad Sci U S A
Prif Awduron:	Raghuram, Viswanathan, Mak, Don-On Daniel, Foskett, J. Kevin
Fformat:	Artigo
Iaith:	Inglês
Cyhoeddwyd:	National Academy of Sciences 2001
Pynciau:	Biological Sciences
Mynediad Ar-lein:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC14749/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11158634/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.031538898
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