Structural and functional similarities between the nucleotide-binding domains of CFTR and GTP-binding proteins
about
Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations.Role of Interaction and Nucleoside Diphosphate Kinase B in Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Function by cAMP-Dependent Protein Kinase A.Gating of cystic fibrosis transmembrane conductance regulator chloride channels by adenosine triphosphate hydrolysis. Quantitative analysis of a cyclic gating schemeOn the mechanism of MgATP-dependent gating of CFTR Cl- channelsRegulation of KATP channel activity by diazoxide and MgADP. Distinct functions of the two nucleotide binding folds of the sulfonylurea receptorDistinct Mg(2+)-dependent steps rate limit opening and closing of a single CFTR Cl(-) channel.Cystic fibrosis transmembrane conductance regulator activation stimulates endosome fusion in vivoReview. ATP hydrolysis-driven gating in cystic fibrosis transmembrane conductance regulator.Alternative splicing of sur2 Exon 17 regulates nucleotide sensitivity of the ATP-sensitive potassium channel.Cytoplasmic loop three of cystic fibrosis transmembrane conductance regulator contributes to regulation of chloride channel activity.Covalent modification of the nucleotide binding domains of cystic fibrosis transmembrane conductance regulator.Mutation of Walker-A lysine 464 in cystic fibrosis transmembrane conductance regulator reveals functional interaction between its nucleotide-binding domains.Inhibition of ATPase, GTPase and adenylate kinase activities of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator by genistein.Mutations that change the position of the putative gamma-phosphate linker in the nucleotide binding domains of CFTR alter channel gating.Dynasore inhibits removal of wild-type and DeltaF508 cystic fibrosis transmembrane conductance regulator (CFTR) from the plasma membrane.Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator.Control of CFTR channel gating by phosphorylation and nucleotide hydrolysis.Dibasic protein kinase A sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator chloride channel.
P2860
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P2860
Structural and functional similarities between the nucleotide-binding domains of CFTR and GTP-binding proteins
description
1995 nî lūn-bûn
@nan
1995 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Structural and functional simi ...... CFTR and GTP-binding proteins
@ast
Structural and functional simi ...... CFTR and GTP-binding proteins
@en
Structural and functional simi ...... CFTR and GTP-binding proteins
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type
label
Structural and functional simi ...... CFTR and GTP-binding proteins
@ast
Structural and functional simi ...... CFTR and GTP-binding proteins
@en
Structural and functional simi ...... CFTR and GTP-binding proteins
@nl
prefLabel
Structural and functional simi ...... CFTR and GTP-binding proteins
@ast
Structural and functional simi ...... CFTR and GTP-binding proteins
@en
Structural and functional simi ...... CFTR and GTP-binding proteins
@nl
P2860
P1433
P1476
Structural and functional simi ...... CFTR and GTP-binding proteins
@en
P2093
P2860
P304
P356
10.1016/S0006-3495(95)80113-X
P407
P577
1995-12-01T00:00:00Z