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Modeling the Conformational Changes Underlying Channel Opening in CFTR

Mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator protein (CFTR) cause cystic fibrosis (CF), the most common life-shortening genetic disease among Caucasians. Although general features of the structure of CFTR have been predicted from homology models, the conform...

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Detalhes bibliográficos
Main Authors: Rahman, Kazi S., Cui, Guiying, Harvey, Stephen C., McCarty, Nael A.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3785483/
https://ncbi.nlm.nih.gov/pubmed/24086355
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0074574
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