Lysine

CF transmembrane conductance regulator ; Homo sapiens







13 Article(s)
Download
PMID
Title
Pub. Year
#Total Relationships
1 35101441 Functionally additive fixed positive and negative charges in the CFTR channel pore control anion binding and conductance. 2022 Mar 2
2 35569794 Opposite regulation of F508del-CFTR biogenesis by four poly-lysine ubiquitin chains In vitro. 2022 Jun 1 4
3 27585394 The Cystic Fibrosis Transmembrane Conductance Regulator Potentiator Ivacaftor Augments Mucociliary Clearance Abrogating Cystic Fibrosis Transmembrane Conductance Regulator Inhibition by Cigarette Smoke. 2017 Jan 1
4 25673337 Location of a permeant anion binding site in the cystic fibrosis transmembrane conductance regulator chloride channel pore. 2015 May 1
5 24777605 Interference with ubiquitination in CFTR modifies stability of core glycosylated and cell surface pools. 2014 Jul 2
6 23083715 Tuning of CFTR chloride channel function by location of positive charges within the pore. 2012 Oct 17 1
7 22030396 FKBP38 peptidylprolyl isomerase promotes the folding of cystic fibrosis transmembrane conductance regulator in the endoplasmic reticulum. 2011 Dec 16 1
8 20551307 Folding and rescue of a cystic fibrosis transmembrane conductance regulator trafficking mutant identified using human-murine chimeric proteins. 2010 Aug 27 2
9 11882668 Mutation of Walker-A lysine 464 in cystic fibrosis transmembrane conductance regulator reveals functional interaction between its nucleotide-binding domains. 2002 Mar 1 1
10 11407896 Nuclear translocation of lactosylated poly-L-lysine/cDNA complex in cystic fibrosis airway epithelial cells. 2001 Jun 1
11 9931011 Walker mutations reveal loose relationship between catalytic and channel-gating activities of purified CFTR (cystic fibrosis transmembrane conductance regulator). 1999 Feb 2 1
12 7694154 Multi-ion pore behaviour in the CFTR chloride channel. 1993 Nov 4 2
13 1712984 Demonstration that CFTR is a chloride channel by alteration of its anion selectivity. 1991 Jul 12 1