113 related articles for article (PubMed ID: 11451963)
1. Requirement of multiple protein domains and residues for gating K(ATP) channels by intracellular pH.
Piao H; Cui N; Xu H; Mao J; Rojas A; Wang R; Abdulkadir L; Li L; Wu J; Jiang C
J Biol Chem; 2001 Sep; 276(39):36673-80. PubMed ID: 11451963
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Direct activation of cloned K(atp) channels by intracellular acidosis.
Xu H; Cui N; Yang Z; Wu J; Giwa LR; Abdulkadir L; Sharma P; Jiang C
J Biol Chem; 2001 Apr; 276(16):12898-902. PubMed ID: 11278532
[TBL] [Abstract][Full Text] [Related]
4. A threonine residue (Thr71) at the intracellular end of the M1 helix plays a critical role in the gating of Kir6.2 channels by intracellular ATP and protons.
Cui N; Wu J; Xu H; Wang R; Rojas A; Piao H; Mao J; Abdulkadir L; Li L; Jiang C
J Membr Biol; 2003 Mar; 192(2):111-22. PubMed ID: 12682799
[TBL] [Abstract][Full Text] [Related]
5. Critical protein domains and amino acid residues for gating the KIR6.2 channel by intracellular ATP.
Wu J; Piao H; Rojas A; Wang R; Wang Y; Cui N; Shi Y; Chen F; Jiang C
J Cell Physiol; 2004 Jan; 198(1):73-81. PubMed ID: 14584046
[TBL] [Abstract][Full Text] [Related]
6. Distinct histidine residues control the acid-induced activation and inhibition of the cloned K(ATP) channel.
Xu H; Wu J; Cui N; Abdulkadir L; Wang R; Mao J; Giwa LR; Chanchevalap S; Jiang C
J Biol Chem; 2001 Oct; 276(42):38690-6. PubMed ID: 11514573
[TBL] [Abstract][Full Text] [Related]
7. pH-dependent modulation of the cloned renal K+ channel, ROMK.
McNicholas CM; MacGregor GG; Islas LD; Yang Y; Hebert SC; Giebisch G
Am J Physiol; 1998 Dec; 275(6):F972-81. PubMed ID: 9843915
[TBL] [Abstract][Full Text] [Related]
8. Protons activate homomeric Kir6.2 channels by selective suppression of the long and intermediate closures.
Wu J; Xu H; Yang Z; Wang Y; Mao J; Jiang C
J Membr Biol; 2002 Nov; 190(2):105-16. PubMed ID: 12474075
[TBL] [Abstract][Full Text] [Related]
9. Inhibition of G-protein-coupled inward rectifying K+ channels by intracellular acidosis.
Mao J; Wu J; Chen F; Wang X; Jiang C
J Biol Chem; 2003 Feb; 278(9):7091-8. PubMed ID: 12501240
[TBL] [Abstract][Full Text] [Related]
10. Gating of inward rectifier K+ channels by proton-mediated interactions of N- and C-terminal domains.
Qu Z; Yang Z; Cui N; Zhu G; Liu C; Xu H; Chanchevalap S; Shen W; Wu J; Li Y; Jiang C
J Biol Chem; 2000 Oct; 275(41):31573-80. PubMed ID: 10896660
[TBL] [Abstract][Full Text] [Related]
11. Tandem function of nucleotide binding domains confers competence to sulfonylurea receptor in gating ATP-sensitive K+ channels.
Zingman LV; Hodgson DM; Bienengraeber M; Karger AB; Kathmann EC; Alekseev AE; Terzic A
J Biol Chem; 2002 Apr; 277(16):14206-10. PubMed ID: 11825892
[TBL] [Abstract][Full Text] [Related]
12. Involvement of the N-terminus of Kir6.2 in the inhibition of the KATP channel by ATP.
Proks P; Gribble FM; Adhikari R; Tucker SJ; Ashcroft FM
J Physiol; 1999 Jan; 514 ( Pt 1)(Pt 1):19-25. PubMed ID: 9831713
[TBL] [Abstract][Full Text] [Related]
13. Remodelling of the SUR-Kir6.2 interface of the KATP channel upon ATP binding revealed by the conformational blocker rhodamine 123.
Hosy E; Dérand R; Revilloud J; Vivaudou M
J Physiol; 2007 Jul; 582(Pt 1):27-39. PubMed ID: 17510180
[TBL] [Abstract][Full Text] [Related]
14. Allosteric modulation of the mouse Kir6.2 channel by intracellular H+ and ATP.
Wu J; Cui N; Piao H; Wang Y; Xu H; Mao J; Jiang C
J Physiol; 2002 Sep; 543(Pt 2):495-504. PubMed ID: 12205184
[TBL] [Abstract][Full Text] [Related]
15. A region of the sulfonylurea receptor critical for a modulation of ATP-sensitive K(+) channels by G-protein betagamma-subunits.
Wada Y; Yamashita T; Imai K; Miura R; Takao K; Nishi M; Takeshima H; Asano T; Morishita R; Nishizawa K; Kokubun S; Nukada T
EMBO J; 2000 Sep; 19(18):4915-25. PubMed ID: 10990455
[TBL] [Abstract][Full Text] [Related]
16. pH-dependent gating of ROMK (Kir1.1) channels involves conformational changes in both N and C termini.
Schulte U; Hahn H; Wiesinger H; Ruppersberg JP; Fakler B
J Biol Chem; 1998 Dec; 273(51):34575-9. PubMed ID: 9852128
[TBL] [Abstract][Full Text] [Related]
17. Identification of a titratable lysine residue that determines sensitivity of kidney potassium channels (ROMK) to intracellular pH.
Fakler B; Schultz JH; Yang J; Schulte U; Brandle U; Zenner HP; Jan LY; Ruppersberg JP
EMBO J; 1996 Aug; 15(16):4093-9. PubMed ID: 8861938
[TBL] [Abstract][Full Text] [Related]
18. A single residue contributes to the difference between Kir4.1 and Kir1.1 channels in pH sensitivity, rectification and single channel conductance.
Xu H; Yang Z; Cui N; Chanchevalap S; Valesky WW; Jiang C
J Physiol; 2000 Oct; 528 Pt 2(Pt 2):267-77. PubMed ID: 11034617
[TBL] [Abstract][Full Text] [Related]
19. Molecular determinants for the distinct pH sensitivity of Kir1.1 and Kir4.1 channels.
Xu H; Yang Z; Cui N; Giwa LR; Abdulkadir L; Patel M; Sharma P; Shan G; Shen W; Jiang C
Am J Physiol Cell Physiol; 2000 Nov; 279(5):C1464-71. PubMed ID: 11029294
[TBL] [Abstract][Full Text] [Related]
20. Role of conserved glycines in pH gating of Kir1.1 (ROMK).
Sackin H; Nanazashvili M; Palmer LG; Li H
Biophys J; 2006 May; 90(10):3582-9. PubMed ID: 16533837
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
