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In vivo phosphorylation of CFTR promotes formation of a nucleotide-binding domain heterodimer

The human ATP-binding cassette (ABC) protein CFTR (cystic fibrosis transmembrane conductance regulator) is a chloride channel, whose dysfunction causes cystic fibrosis. To gain structural insight into the dynamic interaction between CFTR's nucleotide-binding domains (NBDs) proposed to underlie...

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Main Authors: Mense, Martin, Vergani, Paola, White, Dennis M, Altberg, Gal, Nairn, Angus C, Gadsby, David C
Formato: Artigo
Idioma:Inglês
Publicado: 2006
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1618097/
https://ncbi.nlm.nih.gov/pubmed/17036051
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.emboj.7601373
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