Pages that link to "Q45124216"

The following pages link to Determination of the functional unit of the cystic fibrosis transmembrane conductance regulator chloride channel. One polypeptide forms one pore (Q45124216):

Displaying 17 items.

• The ABC protein turned chloride channel whose failure causes cystic fibrosis (Q24657572) (← links)
• Three charged amino acids in extracellular loop 1 are involved in maintaining the outer pore architecture of CFTR. (Q33964059) (← links)
• The block of CFTR by scorpion venom is state-dependent (Q34352436) (← links)
• CFTR: Ligand exchange between a permeant anion ([Au(CN)2]-) and an engineered cysteine (T338C) blocks the pore (Q34984671) (← links)
• Modeling the conformational changes underlying channel opening in CFTR (Q35005061) (← links)
• Recent progress in understanding the mechanism of P-glycoprotein-mediated drug efflux. (Q36386127) (← links)
• Mutations at arginine 352 alter the pore architecture of CFTR. (Q36776120) (← links)
• Three-dimensional reconstruction of human cystic fibrosis transmembrane conductance regulator chloride channel revealed an ellipsoidal structure with orifices beneath the putative transmembrane domain (Q36949400) (← links)
• Two salt bridges differentially contribute to the maintenance of cystic fibrosis transmembrane conductance regulator (CFTR) channel function (Q37012562) (← links)
• Acute inhibition of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel by thyroid hormones involves multiple mechanisms (Q37234590) (← links)
• Cystic fibrosis transmembrane conductance regulator: using differential reactivity toward channel-permeant and channel-impermeant thiol-reactive probes to test a molecular model for the pore (Q42588798) (← links)
• Differential contribution of TM6 and TM12 to the pore of CFTR identified by three sulfonylurea-based blockers (Q42628335) (← links)
• State-dependent chemical reactivity of an engineered cysteine reveals conformational changes in the outer vestibule of the cystic fibrosis transmembrane conductance regulator (Q42670820) (← links)
• A high-field solid-state 35/37Cl NMR and quantum chemical investigation of the chlorine quadrupolar and chemical shift tensors in amino acid hydrochlorides (Q46876154) (← links)
• A possible role for intracellular GSH in spontaneous reaction of a cysteine (T338C) engineered into the Cystic Fibrosis Transmembrane Conductance Regulator (Q48783554) (← links)
• ATP hydrolysis-dependent asymmetry of the conformation of CFTR channel pore. (Q54211454) (← links)
• VX-770-mediated potentiation of numerous human CFTR disease mutants is influenced by phosphorylation level (Q90149884) (← links)