A monomer is the minimum functional unit required for channel and ATPase activity of the cystic fibrosis transmembrane conductance regulator
about
Expression of human electron transfer flavoprotein-ubiquinone oxidoreductase from a baculovirus vector: kinetic and spectral characterization of the human proteinOptimized purification of a heterodimeric ABC transporter in a highly stable form amenable to 2-D crystallizationMonomeric CFTR in plasma membranes in live cells revealed by single molecule fluorescence imaging.Chemical crosslinking studies with the mouse Kcc1 K-Cl cotransporterCystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner.Distinct Mg(2+)-dependent steps rate limit opening and closing of a single CFTR Cl(-) channel.Mutations at arginine 352 alter the pore architecture of CFTR.Three-dimensional reconstruction of human cystic fibrosis transmembrane conductance regulator chloride channel revealed an ellipsoidal structure with orifices beneath the putative transmembrane domainRegulation of function by dimerization through the amino-terminal membrane-spanning domain of human ABCC1/MRP1.Characterization of oligomeric human half-ABC transporter ATP-binding cassette G2.Molecular assembly of cystic fibrosis transmembrane conductance regulator in plasma membrane.Expression and purification of the cystic fibrosis transmembrane conductance regulator protein in Saccharomyces cerevisiaeStable dimeric assembly of the second membrane-spanning domain of CFTR (cystic fibrosis transmembrane conductance regulator) reconstitutes a chloride-selective pore.Dimeric cystic fibrosis transmembrane conductance regulator exists in the plasma membraneProtein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain.Intermolecular interaction between R domains of cystic fibrosis transmembrane conductance regulator.Determination of the functional unit of the cystic fibrosis transmembrane conductance regulator chloride channel. One polypeptide forms one pore.Stoichiometry and novel gating mechanism within the cystic fibrosis transmembrane conductance regulator channel.Genome Sequence of the Freshwater Yangtze Finless Porpoise.
P2860
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P2860
A monomer is the minimum functional unit required for channel and ATPase activity of the cystic fibrosis transmembrane conductance regulator
description
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2001
@ast
im September 2001 veröffentlicher wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel (gepubliceerd op 2001/09/04)
@nl
наукова стаття, опублікована у вересні 2001
@uk
مقالة علمية (نشرت في 4-9-2001)
@ar
name
A monomer is the minimum funct ...... membrane conductance regulator
@ast
A monomer is the minimum funct ...... membrane conductance regulator
@en
type
label
A monomer is the minimum funct ...... membrane conductance regulator
@ast
A monomer is the minimum funct ...... membrane conductance regulator
@en
prefLabel
A monomer is the minimum funct ...... membrane conductance regulator
@ast
A monomer is the minimum funct ...... membrane conductance regulator
@en
P2093
P921
P356
P1433
P1476
A monomer is the minimum funct ...... membrane conductance regulator
@en
P2093
P304
10700–10706
P356
10.1021/BI0108195
P407
P577
2001-09-04T00:00:00Z