255 related articles for article (PubMed ID: 32102849)
1. Protein kinase A phosphorylation potentiates cystic fibrosis transmembrane conductance regulator gating by relieving autoinhibition on the stimulatory C terminus of the regulatory domain.
Chen JH
J Biol Chem; 2020 Apr; 295(14):4577-4590. PubMed ID: 32102849
[TBL] [Abstract][Full Text] [Related]
2. Severed channels probe regulation of gating of cystic fibrosis transmembrane conductance regulator by its cytoplasmic domains.
Csanády L; Chan KW; Seto-Young D; Kopsco DC; Nairn AC; Gadsby DC
J Gen Physiol; 2000 Sep; 116(3):477-500. PubMed ID: 10962022
[TBL] [Abstract][Full Text] [Related]
3. A cluster of negative charges at the amino terminal tail of CFTR regulates ATP-dependent channel gating.
Fu J; Ji HL; Naren AP; Kirk KL
J Physiol; 2001 Oct; 536(Pt 2):459-70. PubMed ID: 11600681
[TBL] [Abstract][Full Text] [Related]
4. Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels.
Wang F; Zeltwanger S; Hu S; Hwang TC
J Physiol; 2000 May; 524 Pt 3(Pt 3):637-48. PubMed ID: 10790148
[TBL] [Abstract][Full Text] [Related]
5. An electrostatic interaction at the tetrahelix bundle promotes phosphorylation-dependent cystic fibrosis transmembrane conductance regulator (CFTR) channel opening.
Wang W; Roessler BC; Kirk KL
J Biol Chem; 2014 Oct; 289(44):30364-30378. PubMed ID: 25190805
[TBL] [Abstract][Full Text] [Related]
6. Regulation of recombinant cardiac cystic fibrosis transmembrane conductance regulator chloride channels by protein kinase C.
Yamazaki J; Britton F; Collier ML; Horowitz B; Hume JR
Biophys J; 1999 Apr; 76(4):1972-87. PubMed ID: 10096895
[TBL] [Abstract][Full Text] [Related]
7. Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain.
Howell LD; Borchardt R; Kole J; Kaz AM; Randak C; Cohn JA
Biochem J; 2004 Feb; 378(Pt 1):151-9. PubMed ID: 14602047
[TBL] [Abstract][Full Text] [Related]
8. Simple binding of protein kinase A prior to phosphorylation allows CFTR anion channels to be opened by nucleotides.
Mihályi C; Iordanov I; Töröcsik B; Csanády L
Proc Natl Acad Sci U S A; 2020 Sep; 117(35):21740-21746. PubMed ID: 32817533
[TBL] [Abstract][Full Text] [Related]
9. Preferential phosphorylation of R-domain Serine 768 dampens activation of CFTR channels by PKA.
Csanády L; Seto-Young D; Chan KW; Cenciarelli C; Angel BB; Qin J; McLachlin DT; Krutchinsky AN; Chait BT; Nairn AC; Gadsby DC
J Gen Physiol; 2005 Feb; 125(2):171-86. PubMed ID: 15657296
[TBL] [Abstract][Full Text] [Related]
10. Stimulation of CFTR activity by its phosphorylated R domain.
Winter MC; Welsh MJ
Nature; 1997 Sep; 389(6648):294-6. PubMed ID: 9305845
[TBL] [Abstract][Full Text] [Related]
11. Differential sensitivity of the cystic fibrosis (CF)-associated mutants G551D and G1349D to potentiators of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel.
Cai Z; Taddei A; Sheppard DN
J Biol Chem; 2006 Jan; 281(4):1970-7. PubMed ID: 16311240
[TBL] [Abstract][Full Text] [Related]
12. G551D mutation impairs PKA-dependent activation of CFTR channel that can be restored by novel GOF mutations.
Wang W; Fu L; Liu Z; Wen H; Rab A; Hong JS; Kirk KL; Rowe SM
Am J Physiol Lung Cell Mol Physiol; 2020 Nov; 319(5):L770-L785. PubMed ID: 32877225
[TBL] [Abstract][Full Text] [Related]
13. Curcumin opens cystic fibrosis transmembrane conductance regulator channels by a novel mechanism that requires neither ATP binding nor dimerization of the nucleotide-binding domains.
Wang W; Bernard K; Li G; Kirk KL
J Biol Chem; 2007 Feb; 282(7):4533-4544. PubMed ID: 17178710
[TBL] [Abstract][Full Text] [Related]
14. Removal of the Fe(iii) site promotes activation of the human cystic fibrosis transmembrane conductance regulator by high-affinity Zn(ii) binding.
Wang G
Metallomics; 2018 Feb; 10(2):240-247. PubMed ID: 29372915
[TBL] [Abstract][Full Text] [Related]
15. Molecular Basis for Fe(III)-Independent Curcumin Potentiation of Cystic Fibrosis Transmembrane Conductance Regulator Activity.
Wang G
Biochemistry; 2015 May; 54(18):2828-40. PubMed ID: 25867080
[TBL] [Abstract][Full Text] [Related]
16. Functional roles of nonconserved structural segments in CFTR's NH2-terminal nucleotide binding domain.
Csanády L; Chan KW; Nairn AC; Gadsby DC
J Gen Physiol; 2005 Jan; 125(1):43-55. PubMed ID: 15596536
[TBL] [Abstract][Full Text] [Related]
17. The inhibition mechanism of non-phosphorylated Ser768 in the regulatory domain of cystic fibrosis transmembrane conductance regulator.
Wang G
J Biol Chem; 2011 Jan; 286(3):2171-82. PubMed ID: 21059651
[TBL] [Abstract][Full Text] [Related]
18. cAMP-dependent protein kinase-mediated phosphorylation of cystic fibrosis transmembrane conductance regulator residue Ser-753 and its role in channel activation.
Seibert FS; Tabcharani JA; Chang XB; Dulhanty AM; Mathews C; Hanrahan JW; Riordan JR
J Biol Chem; 1995 Feb; 270(5):2158-62. PubMed ID: 7530719
[TBL] [Abstract][Full Text] [Related]
19. Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by negative charge in the R domain.
Rich DP; Berger HA; Cheng SH; Travis SM; Saxena M; Smith AE; Welsh MJ
J Biol Chem; 1993 Sep; 268(27):20259-67. PubMed ID: 7690753
[TBL] [Abstract][Full Text] [Related]
20. Mutating the Conserved Q-loop Glutamine 1291 Selectively Disrupts Adenylate Kinase-dependent Channel Gating of the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Reduces Channel Function in Primary Human Airway Epithelia.
Dong Q; Ernst SE; Ostedgaard LS; Shah VS; Ver Heul AR; Welsh MJ; Randak CO
J Biol Chem; 2015 May; 290(22):14140-53. PubMed ID: 25887396
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]