Cargando…
Structural models of CFTR–AMPK and CFTR–PKA interactions: R-domain flexibility is a key factor in CFTR regulation
Cystic fibrosis (CF), the most common lethal genetic disease among Caucasians, is caused by mutations in cystic fibrosis transmembrane conductance regulator (CFTR). CFTR’s main role is to transport chloride ions across epithelial cell membranes. It also regulates many cell functions. However, the ex...
Autores principales: | Siwiak, Marian, Edelman, Aleksander, Zielenkiewicz, Piotr |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249538/ https://www.ncbi.nlm.nih.gov/pubmed/21455600 http://dx.doi.org/10.1007/s00894-011-1029-0 |
Ejemplares similares
-
Characterization of Nasal Potential Difference in cftr Knockout and F508del-CFTR Mice
por: Saussereau, Emilie Lyne, et al.
Publicado: (2013) -
CFTR mutations altering CFTR fragmentation
por: Tosoni, Kendra, et al.
Publicado: (2012) -
Preferential Phosphorylation of R-domain Serine 768 Dampens Activation of CFTR Channels by PKA
por: Csanády, László, et al.
Publicado: (2005) -
Mechanistic Insight into Control of CFTR by
AMPK
por: Kongsuphol, Patthara, et al.
Publicado: (2009) -
CFTR Gating I: Characterization of the ATP-dependent Gating of a Phosphorylation-independent CFTR Channel (ΔR-CFTR)
por: Bompadre, Silvia G., et al.
Publicado: (2005)