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Mutant cycles at CFTR’s non-canonical ATP-binding site support little interface separation during gating
Cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel belonging to the adenosine triphosphate (ATP)-binding cassette (ABC) superfamily. ABC proteins share a common molecular mechanism that couples ATP binding and hydrolysis at two nucleotide-binding domains (NBDs) to diver...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The Rockefeller University Press
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3105517/ https://ncbi.nlm.nih.gov/pubmed/21576373 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.201110608 |
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