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CONTROL OF THE CFTR CHANNEL’S GATES

Unique among ABC (ATP-binding cassette) protein family members, CFTR (cystic fibrosis transmembrane conductance regulator), encoded by the gene mutated in cystic fibrosis patients, functions as an ion channel. Opening and closing of its anion-selective pore are linked to ATP binding and hydrolysis a...

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Detalhes bibliográficos
Main Authors: Vergani, Paola, Basso, Claudia, Mense, Martin, Nairn, Angus C., Gadsby, David C.
Formato: Artigo
Idioma:Inglês
Publicado em: 2005
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2728124/
https://ncbi.nlm.nih.gov/pubmed/16246032
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BST20051003
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