human CFTR NBD1 deltaRI F508del mutant chemical shift assignments

Deletion of Phenylalanine 508 in the First Nucleotide-binding Domain of the Cystic Fibrosis Transmembrane Conductance Regulator Increases Conformational Exchange and Inhibits Dimerization.

Conformational changes relevant to channel activity and folding within the first nucleotide binding domain of the cystic fibrosis transmembrane conductance regulator.

chemical shift assignments for a protein construct comprising residues 387-404 and 437-646 of human CFTR with F508del mutation