Cystic Fibrosis Transmembrane Conductance Regulator Interacts with Multiple Immunoglobulin Domains of Filamin A

Mutations of the chloride channel cystic fibrosis transmembrane conductance regulator (CFTR) that impair its apical localization and function cause cystic fibrosis. A previous report has shown that filamin A (FLNa), an actin-cross-linking and -scaffolding protein, interacts directly with the cytopla...

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Detalhes bibliográficos
Main Authors: Playford, Martin P., Nurminen, Elisa, Pentikäinen, Olli T., Milgram, Sharon L., Hartwig, John H., Stossel, Thomas P., Nakamura, Fumihiko
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2010
Assuntos:
Protein Structure and Folding
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2878090/
https://ncbi.nlm.nih.gov/pubmed/20351098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M109.080523
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