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4. Localization of the ATP/phosphatidylinositol 4,5 diphosphate-binding site to a 39-amino acid region of the carboxyl terminus of the ATP-regulated K+ channel Kir1.1. Dong K; Tang L; MacGregor GG; Hebert SC J Biol Chem; 2002 Dec; 277(51):49366-73. PubMed ID: 12381730 [TBL] [Abstract][Full Text] [Related]
5. Conformational dynamics of the ligand-binding domain of inward rectifier K channels as revealed by molecular dynamics simulations: toward an understanding of Kir channel gating. Haider S; Grottesi A; Hall BA; Ashcroft FM; Sansom MS Biophys J; 2005 May; 88(5):3310-20. PubMed ID: 15749783 [TBL] [Abstract][Full Text] [Related]
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7. Phosphoinositides decrease ATP sensitivity of the cardiac ATP-sensitive K(+) channel. A molecular probe for the mechanism of ATP-sensitive inhibition. Fan Z; Makielski JC J Gen Physiol; 1999 Aug; 114(2):251-69. PubMed ID: 10436001 [TBL] [Abstract][Full Text] [Related]
9. The kinetic and physical basis of K(ATP) channel gating: toward a unified molecular understanding. Enkvetchakul D; Loussouarn G; Makhina E; Shyng SL; Nichols CG Biophys J; 2000 May; 78(5):2334-48. PubMed ID: 10777731 [TBL] [Abstract][Full Text] [Related]
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11. Proximal C-terminal domain of sulphonylurea receptor 2A interacts with pore-forming Kir6 subunits in KATP channels. Rainbow RD; James M; Hudman D; Al Johi M; Singh H; Watson PJ; Ashmole I; Davies NW; Lodwick D; Norman RI Biochem J; 2004 Apr; 379(Pt 1):173-81. PubMed ID: 14672537 [TBL] [Abstract][Full Text] [Related]
12. Synergistic activation of G protein-gated inwardly rectifying potassium channels by the betagamma subunits of G proteins and Na(+) and Mg(2+) ions. Petit-Jacques J; Sui JL; Logothetis DE J Gen Physiol; 1999 Nov; 114(5):673-84. PubMed ID: 10532964 [TBL] [Abstract][Full Text] [Related]
13. Homology modeling and molecular dynamics simulation studies of an inward rectifier potassium channel. Capener CE; Shrivastava IH; Ranatunga KM; Forrest LR; Smith GR; Sansom MS Biophys J; 2000 Jun; 78(6):2929-42. PubMed ID: 10827973 [TBL] [Abstract][Full Text] [Related]
14. Two critical cysteine residues implicated in disulfide bond formation and proper folding of Kir2.1. Cho HC; Tsushima RG; Nguyen TT; Guy HR; Backx PH Biochemistry; 2000 Apr; 39(16):4649-57. PubMed ID: 10769120 [TBL] [Abstract][Full Text] [Related]
15. Cytoplasmic terminus domains of Kir6.x confer different nucleotide-dependent gating on the ATP-sensitive K+ channel. Takano M; Xie LH; Otani H; Horie M J Physiol; 1998 Oct; 512 ( Pt 2)(Pt 2):395-406. PubMed ID: 9763630 [TBL] [Abstract][Full Text] [Related]
16. The pore helix is involved in stabilizing the open state of inwardly rectifying K+ channels. Alagem N; Yesylevskyy S; Reuveny E Biophys J; 2003 Jul; 85(1):300-12. PubMed ID: 12829485 [TBL] [Abstract][Full Text] [Related]
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19. Residues beyond the selectivity filter of the K+ channel kir2.1 regulate permeation and block by external Rb+ and Cs+. Thompson GA; Leyland ML; Ashmole I; Sutcliffe MJ; Stanfield PR J Physiol; 2000 Jul; 526 Pt 2(Pt 2):231-40. PubMed ID: 10896714 [TBL] [Abstract][Full Text] [Related]
20. Coupling Gbetagamma-dependent activation to channel opening via pore elements in inwardly rectifying potassium channels. Sadja R; Smadja K; Alagem N; Reuveny E Neuron; 2001 Mar; 29(3):669-80. PubMed ID: 11301026 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]