CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains.
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Cystic Fibrosis: Lessons from the Sweat GlandDeletion of Phe508 in the first nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator increases its affinity for the heat shock cognate 70 chaperoneTMEM16A(a)/anoctamin-1 shares a homodimeric architecture with CLC chloride channelsThe ABC protein turned chloride channel whose failure causes cystic fibrosisCFTR gating II: Effects of nucleotide binding on the stability of open statesThe Nucleotide-Binding Sites of SUR1: A Mechanistic ModelMolecular action of sulphonylureas on KATP channels: a real partnership between drugs and nucleotidesNeuroprotective role of ATP-sensitive potassium channels in cerebral ischemiaIntegrated analysis of residue coevolution and protein structure in ABC transportersStructures of a minimal human CFTR first nucleotide-binding domain as a monomer, head-to-tail homodimer, and pathogenic mutantABC ATPase signature helices in Rad50 link nucleotide state to Mre11 interface for DNA repair.Snapshots of the maltose transporter during ATP hydrolysisThe Cystic Fibrosis Transmembrane Conductance Regulator (CFTR): THREE-DIMENSIONAL STRUCTURE AND LOCALIZATION OF A CHANNEL GATEKinetics of the Association/Dissociation Cycle of an ATP-binding Cassette Nucleotide-binding DomainRequirements for Efficient Correction of ΔF508 CFTR Revealed by Analyses of Evolved SequencesEttA regulates translation by binding the ribosomal E site and restricting ribosome-tRNA dynamicsThe ABC-F protein EttA gates ribosome entry into the translation elongation cycleDomain and nucleotide dependence of the interaction between Saccharomyces cerevisiae translation elongation factors 3 and 1A.Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectivesThe proposed channel-enzyme transient receptor potential melastatin 2 does not possess ADP ribose hydrolase activityThe primary folding defect and rescue of ΔF508 CFTR emerge during translation of the mutant domainAllosteric coupling between the intracellular coupling helix 4 and regulatory sites of the first nucleotide-binding domain of CFTRRobust Stimulation of W1282X-CFTR Channel Activity by a Combination of Allosteric ModulatorsTetrameric structure of SUR2B revealed by electron microscopy of oriented single particlesThe silent codon change I507-ATC->ATT contributes to the severity of the ΔF508 CFTR channel dysfunctionObligate coupling of CFTR pore opening to tight nucleotide-binding domain dimerizationCurcumin and genistein: the combined effects on disease-associated CFTR mutants and their clinical implicationsDetermination of the quaternary structure of a bacterial ATP-binding cassette (ABC) transporter in living cellsImpact of the F508del mutation on ovine CFTR, a Cl- channel with enhanced conductance and ATP-dependent gating.The cystic fibrosis transmembrane conductance regulator (CFTR) and its stabilityStabilization of Nucleotide Binding Domain Dimers Rescues ABCC6 Mutants Associated with Pseudoxanthoma Elasticum.Development of CFTR StructureATP and AMP mutually influence their interaction with the ATP-binding cassette (ABC) adenylate kinase cystic fibrosis transmembrane conductance regulator (CFTR) at separate binding sites.Small molecule correctors of F508del-CFTR discovered by structure-based virtual screeningFolding and rescue of a cystic fibrosis transmembrane conductance regulator trafficking mutant identified using human-murine chimeric proteinsCFTR and TNR-CFTR expression and function in the kidney.Cystic fibrosis: exploiting its genetic basis in the hunt for new therapiesStrict coupling between CFTR's catalytic cycle and gating of its Cl- ion pore revealed by distributions of open channel burst durations.ATP-independent CFTR channel gating and allosteric modulation by phosphorylation.The H-loop in the second nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator is required for efficient chloride channel closing
P2860
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P2860
CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains.
@en
CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains.
@nl
type
label
CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains.
@en
CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains.
@nl
prefLabel
CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains.
@en
CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains.
@nl
P2860
P356
P1433
P1476
CFTR channel opening by ATP-driven tight dimerization of its nucleotide-binding domains.
@en
P2093
David C Gadsby
Steve W Lockless
P2860
P2888
P304
P356
10.1038/NATURE03313
P407
P577
2005-02-01T00:00:00Z
P5875
P6179
1027581213