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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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| Auteurs principaux: | , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2005
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| Sujets: | |
| Accès en ligne: | 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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