Silver as a probe of pore-forming residues in a potassium channel

Q Lü, C Miller - Science, 1995 - science.org
In voltage-dependent potassium channels, the molecular determinants of ion selectivity are
found in the P (pore) region, a stretch of 21 contiguous residues. Cysteine was introduced at …

A cysteine residue in the third membrane-spanning segment of the human D2 dopamine receptor is exposed in the binding-site crevice.

JA Javitch, X Li, J Kaback… - Proceedings of the …, 1994 - National Acad Sciences
The binding site in G-protein-linked neurotransmitter receptors is formed among their
membrane-spanning segments. Because the binding site is in the plane of the bilayer and is …

[HTML][HTML] Cystic fibrosis-associated mutations at arginine 347 alter the pore architecture of CFTR: evidence for disruption of a salt bridge

JF Cotten, MJ Welsh - Journal of Biological Chemistry, 1999 - ASBMB
Arginine 347 in the sixth transmembrane domain of cystic fibrosis transmembrane
conductance regulator (CFTR) is a site of four cystic fibrosis-associated mutations. To better …

[HTML][HTML] Molecular determinants of anion selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel pore

P Linsdell, A Evagelidis, JW Hanrahan - Biophysical Journal, 2000 - cell.com
Ionic selectivity in many cation channels is achieved over a short region of the pore known
as the selectivity filter, the molecular determinants of which have been identified in Ca 2+ …

Permeation through the CFTR chloride channel

NA Mccarty - Journal of Experimental Biology, 2000 - journals.biologists.com
The cystic fibrosis transmembrane conductance regulator (CFTR) protein forms a Cl−
channel found in the plasma membranes of many epithelial cells, including those of the …

Transmembrane segment 1 of human P-glycoprotein contributes to the drug-binding pocket

TW Loo, MC Bartlett, DM Clarke - Biochemical Journal, 2006 - portlandpress.com
P-glycoprotein (P-gp; ABCB1) actively transports a broad range of structurally unrelated
compounds out of the cell. An important step in the transport cycle is coupling of drug …

Molecular modelling and molecular dynamics of CFTR

I Callebaut, B Hoffmann, P Lehn, JP Mornon - Cellular and Molecular Life …, 2017 - Springer
The cystic fibrosis transmembrane conductance regulator (CFTR) protein is a member of the
ATP-binding cassette (ABC) transporter superfamily that functions as an ATP-gated channel …

[HTML][HTML] Serotonin and cocaine-sensitive inactivation of human serotonin transporters by methanethiosulfonates targeted to transmembrane domain I

LK Henry, EM Adkins, Q Han, RD Blakely - Journal of Biological Chemistry, 2003 - ASBMB
To explore aqueous accessibility and functional contributions of transmembrane domain
(TM) 1 in human serotonin transporter (hSERT) proteins, we utilized the largely …

CFTR: covalent and noncovalent modification suggests a role for fixed charges in anion conduction

SS Smith, X Liu, ZR Zhang, F Sun, TE Kriewall… - The Journal of General …, 2001 - rupress.org
The goal of the experiments described here was to explore the possible role of fixed charges
in determining the conduction properties of CFTR. We focused on transmembrane segment …

Functional architecture of the CFTR chloride channel

P Linsdell - Molecular membrane biology, 2014 - Taylor & Francis
Cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance
regulator (CFTR), a member of the ATP-binding cassette (ABC) family of membrane …