214 related articles for article (PubMed ID: 23078514)
1. NMR and fluorescence studies of drug binding to the first nucleotide binding domain of SUR2A.
López-Alonso JP; de Araujo ED; Kanelis V
Biochemistry; 2012 Nov; 51(45):9211-22. PubMed ID: 23078514
[TBL] [Abstract][Full Text] [Related]
2. A functional role of the C-terminal 42 amino acids of SUR2A and SUR2B in the physiology and pharmacology of cardiovascular ATP-sensitive K(+) channels.
Yamada M; Kurachi Y
J Mol Cell Cardiol; 2005 Jul; 39(1):1-6. PubMed ID: 15978900
[TBL] [Abstract][Full Text] [Related]
3. Potassium channel openers require ATP to bind to and act through sulfonylurea receptors.
Schwanstecher M; Sieverding C; Dörschner H; Gross I; Aguilar-Bryan L; Schwanstecher C; Bryan J
EMBO J; 1998 Oct; 17(19):5529-35. PubMed ID: 9755153
[TBL] [Abstract][Full Text] [Related]
4. Successful development and use of a thermodynamic stability screen for optimizing the yield of nucleotide binding domains.
de Araujo ED; Kanelis V
Protein Expr Purif; 2014 Nov; 103():38-47. PubMed ID: 25153533
[TBL] [Abstract][Full Text] [Related]
5. Characterization of K(ATP)-channels in rat basilar and middle cerebral arteries: studies of vasomotor responses and mRNA expression.
Jansen-Olesen I; Mortensen CH; El-Bariaki N; Ploug KB
Eur J Pharmacol; 2005 Oct; 523(1-3):109-18. PubMed ID: 16226739
[TBL] [Abstract][Full Text] [Related]
6. Mutation in nucleotide-binding domains of sulfonylurea receptor 2 evokes Na-ATP-dependent activation of ATP-sensitive K+ channels: implication for dimerization of nucleotide-binding domains to induce channel opening.
Yamada M; Ishii M; Hibino H; Kurachi Y
Mol Pharmacol; 2004 Oct; 66(4):807-16. PubMed ID: 15258252
[TBL] [Abstract][Full Text] [Related]
7. Coassembly of different sulfonylurea receptor subtypes extends the phenotypic diversity of ATP-sensitive potassium (KATP) channels.
Wheeler A; Wang C; Yang K; Fang K; Davis K; Styer AM; Mirshahi U; Moreau C; Revilloud J; Vivaudou M; Liu S; Mirshahi T; Chan KW
Mol Pharmacol; 2008 Nov; 74(5):1333-44. PubMed ID: 18723823
[TBL] [Abstract][Full Text] [Related]
8. Differential response of K(ATP) channels containing SUR2A or SUR2B subunits to nucleotides and pinacidil.
Reimann F; Gribble FM; Ashcroft FM
Mol Pharmacol; 2000 Dec; 58(6):1318-25. PubMed ID: 11093769
[TBL] [Abstract][Full Text] [Related]
9. The Kir6.2-F333I mutation differentially modulates KATP channels composed of SUR1 or SUR2 subunits.
Tammaro P; Ashcroft F
J Physiol; 2007 Jun; 581(Pt 3):1259-69. PubMed ID: 17395632
[TBL] [Abstract][Full Text] [Related]
10. The ATPase activities of sulfonylurea receptor 2A and sulfonylurea receptor 2B are influenced by the C-terminal 42 amino acids.
de Wet H; Fotinou C; Amad N; Dreger M; Ashcroft FM
FEBS J; 2010 Jun; 277(12):2654-62. PubMed ID: 20553499
[TBL] [Abstract][Full Text] [Related]
11. C-terminal tails of sulfonylurea receptors control ADP-induced activation and diazoxide modulation of ATP-sensitive K(+) channels.
Matsuoka T; Matsushita K; Katayama Y; Fujita A; Inageda K; Tanemoto M; Inanobe A; Yamashita S; Matsuzawa Y; Kurachi Y
Circ Res; 2000 Nov; 87(10):873-80. PubMed ID: 11073882
[TBL] [Abstract][Full Text] [Related]
12. Interaction of asymmetric ABCC9-encoded nucleotide binding domains determines KATP channel SUR2A catalytic activity.
Park S; Lim BB; Perez-Terzic C; Mer G; Terzic A
J Proteome Res; 2008 Apr; 7(4):1721-8. PubMed ID: 18311911
[TBL] [Abstract][Full Text] [Related]
13. Differential nucleotide regulation of KATP channels by SUR1 and SUR2A.
Masia R; Enkvetchakul D; Nichols CG
J Mol Cell Cardiol; 2005 Sep; 39(3):491-501. PubMed ID: 15893323
[TBL] [Abstract][Full Text] [Related]
14. SUR2 subtype (A and B)-dependent differential activation of the cloned ATP-sensitive K+ channels by pinacidil and nicorandil.
Shindo T; Yamada M; Isomoto S; Horio Y; Kurachi Y
Br J Pharmacol; 1998 Jul; 124(5):985-91. PubMed ID: 9692785
[TBL] [Abstract][Full Text] [Related]
15. A transmembrane domain of the sulfonylurea receptor mediates activation of ATP-sensitive K(+) channels by K(+) channel openers.
D'hahan N; Jacquet H; Moreau C; Catty P; Vivaudou M
Mol Pharmacol; 1999 Aug; 56(2):308-15. PubMed ID: 10419549
[TBL] [Abstract][Full Text] [Related]
16. Electrophysiological and pharmacological characterization of the K(ATP) channel involved in the K+-current responses to FSH and adenosine in the follicular cells of Xenopus oocyte.
Fujita R; Kimura S; Kawasaki S; Watanabe S; Watanabe N; Hirano H; Matsumoto M; Sasaki K
J Physiol Sci; 2007 Feb; 57(1):51-61. PubMed ID: 17239259
[TBL] [Abstract][Full Text] [Related]
17. The first nucleotide binding domain of the sulfonylurea receptor 2A contains regulatory elements and is folded and functions as an independent module.
de Araujo ED; Ikeda LK; Tzvetkova S; Kanelis V
Biochemistry; 2011 Aug; 50(31):6655-66. PubMed ID: 21714514
[TBL] [Abstract][Full Text] [Related]
18. The N-terminal transmembrane domain (TMD0) and a cytosolic linker (L0) of sulphonylurea receptor define the unique intrinsic gating of KATP channels.
Fang K; Csanády L; Chan KW
J Physiol; 2006 Oct; 576(Pt 2):379-89. PubMed ID: 16887879
[TBL] [Abstract][Full Text] [Related]
19. Analysis of the differential modulation of sulphonylurea block of beta-cell and cardiac ATP-sensitive K+ (K(ATP)) channels by Mg-nucleotides.
Reimann F; Dabrowski M; Jones P; Gribble FM; Ashcroft FM
J Physiol; 2003 Feb; 547(Pt 1):159-68. PubMed ID: 12562963
[TBL] [Abstract][Full Text] [Related]
20. Pharmaco-topology of sulfonylurea receptors. Separate domains of the regulatory subunits of K(ATP) channel isoforms are required for selective interaction with K(+) channel openers.
Babenko AP; Gonzalez G; Bryan J
J Biol Chem; 2000 Jan; 275(2):717-20. PubMed ID: 10625598
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]