Article
Phosphorylation site independent single R-domain mutations affect CFTR channel activity.
FEBS letters - 13 Nov 1998
Wei L, Vankeerberghen A, Cuppens H, Droogmans G, Cassiman J J, Nilius B
Abstract excerpt
We investigated CFTR channel activity of mature R-domain mutants showing single alterations at sites other than the predicted phosphorylation sites. All mutations were found in cystic fibrosis (CF) patients (H620Q, E822K and E826K). The macroscopic CFTR chloride conductance induced by phosphoryla...
Topics
- Animals
- Anions
- COS Cells
- Cystic Fibrosis Transmembrane Conductance Regulator
- Humans
- Ion Transport
- Mutation
- Oocytes
- Phosphorylation
- Protein Conformation
- Xenopus
