177 related articles for article (PubMed ID: 21454663)
1. Rings of charge within the extracellular vestibule influence ion permeation of the 5-HT3A receptor.
Livesey MR; Cooper MA; Lambert JJ; Peters JA
J Biol Chem; 2011 May; 286(18):16008-17. PubMed ID: 21454663
[TBL] [Abstract][Full Text] [Related]
2. Structural determinants of Ca2+ permeability and conduction in the human 5-hydroxytryptamine type 3A receptor.
Livesey MR; Cooper MA; Deeb TZ; Carland JE; Kozuska J; Hales TG; Lambert JJ; Peters JA
J Biol Chem; 2008 Jul; 283(28):19301-13. PubMed ID: 18474595
[TBL] [Abstract][Full Text] [Related]
3. Role of aspartate 298 in mouse 5-HT3A receptor gating and modulation by extracellular Ca2+.
Hu XQ; Lovinger DM
J Physiol; 2005 Oct; 568(Pt 2):381-96. PubMed ID: 16096341
[TBL] [Abstract][Full Text] [Related]
4. 5-HT3 receptor ion size selectivity is a property of the transmembrane channel, not the cytoplasmic vestibule portals.
McKinnon NK; Reeves DC; Akabas MH
J Gen Physiol; 2011 Oct; 138(4):453-66. PubMed ID: 21948949
[TBL] [Abstract][Full Text] [Related]
5. Cation-selective mutations in the M2 domain of the inhibitory glycine receptor channel reveal determinants of ion-charge selectivity.
Keramidas A; Moorhouse AJ; Pierce KD; Schofield PR; Barry PH
J Gen Physiol; 2002 May; 119(5):393-410. PubMed ID: 11981020
[TBL] [Abstract][Full Text] [Related]
6. Conversion of the ion selectivity of the 5-HT(3a) receptor from cationic to anionic reveals a conserved feature of the ligand-gated ion channel superfamily.
Gunthorpe MJ; Lummis SC
J Biol Chem; 2001 Jun; 276(24):10977-83. PubMed ID: 11439930
[TBL] [Abstract][Full Text] [Related]
7. The L293 residue in transmembrane domain 2 of the 5-HT3A receptor is a molecular determinant of allosteric modulation by 5-hydroxyindole.
Hu XQ; Lovinger DM
Neuropharmacology; 2008 Jun; 54(8):1153-65. PubMed ID: 18436267
[TBL] [Abstract][Full Text] [Related]
8. The 5-hydroxytryptamine type 3 (5-HT3) receptor reveals a novel determinant of single-channel conductance.
Peters JA; Kelley SP; Dunlop JI; Kirkness EF; Hales TG; Lambert JJ
Biochem Soc Trans; 2004 Jun; 32(Pt3):547-52. PubMed ID: 15157181
[TBL] [Abstract][Full Text] [Related]
9. Impact of intracellular domain flexibility upon properties of activated human 5-HT3 receptors.
Kozuska JL; Paulsen IM; Belfield WJ; Martin IL; Cole DJ; Holt A; Dunn SM
Br J Pharmacol; 2014 Apr; 171(7):1617-28. PubMed ID: 24283776
[TBL] [Abstract][Full Text] [Related]
10. Dynamic modification of a mutant cytoplasmic cysteine residue modulates the conductance of the human 5-HT3A receptor.
Deeb TZ; Carland JE; Cooper MA; Livesey MR; Lambert JJ; Peters JA; Hales TG
J Biol Chem; 2007 Mar; 282(9):6172-82. PubMed ID: 17200121
[TBL] [Abstract][Full Text] [Related]
11. Mutagenic analysis of the intracellular portals of the human 5-HT3A receptor.
Carland JE; Cooper MA; Livesey MR; Hales TG; Peters JA; Lambert JJ
J Biol Chem; 2013 Nov; 288(44):31592-601. PubMed ID: 24030822
[TBL] [Abstract][Full Text] [Related]
12. Direct interaction of the resistance to inhibitors of cholinesterase type 3 protein with the serotonin receptor type 3A intracellular domain.
Nishtala SN; Mnatsakanyan N; Pandhare A; Leung C; Jansen M
J Neurochem; 2016 May; 137(4):528-38. PubMed ID: 26875553
[TBL] [Abstract][Full Text] [Related]
13. On the structural basis for size-selective permeation of organic cations through the voltage-gated sodium channel. Effect of alanine mutations at the DEKA locus on selectivity, inhibition by Ca2+ and H+, and molecular sieving.
Sun YM; Favre I; Schild L; Moczydlowski E
J Gen Physiol; 1997 Dec; 110(6):693-715. PubMed ID: 9382897
[TBL] [Abstract][Full Text] [Related]
14. Identification of pore residues engaged in determining divalent cationic permeation in transient receptor potential melastatin subtype channel 2.
Xia R; Mei ZZ; Mao HJ; Yang W; Dong L; Bradley H; Beech DJ; Jiang LH
J Biol Chem; 2008 Oct; 283(41):27426-27432. PubMed ID: 18687688
[TBL] [Abstract][Full Text] [Related]
15. Ethanol stabilizes the open state of single 5-hydroxytryptamine(3A)(QDA) receptors.
Feinberg-Zadek PL; Davies PA
J Pharmacol Exp Ther; 2010 Jun; 333(3):896-902. PubMed ID: 20200118
[TBL] [Abstract][Full Text] [Related]
16. Conversion of the ion selectivity of the 5-HT(3a) receptor from cationic to anionic reveals a conserved feature of the ligand-gated ion channel superfamily.
Gunthorpe MJ; Lummis SC
J Biol Chem; 2001 Apr; 276(14):10977-83. PubMed ID: 11139582
[TBL] [Abstract][Full Text] [Related]
17. Pathways and Barriers for Ion Translocation through the 5-HT3A Receptor Channel.
Di Maio D; Chandramouli B; Brancato G
PLoS One; 2015; 10(10):e0140258. PubMed ID: 26465896
[TBL] [Abstract][Full Text] [Related]
18. Conformational Changes in the 5-HT
Munro L; Ladefoged LK; Padmanathan V; Andersen S; Schiøtt B; Kristensen AS
Mol Pharmacol; 2019 Dec; 96(6):720-734. PubMed ID: 31582575
[TBL] [Abstract][Full Text] [Related]
19. Resveratrol enhances 5-hydroxytryptamine type 3A receptor-mediated ion currents: the role of arginine 222 residue in pre-transmembrane domain I.
Lee BH; Hwang SH; Choi SH; Shin TJ; Kang J; Lee SM; Nah SY
Biol Pharm Bull; 2011; 34(4):523-7. PubMed ID: 21467640
[TBL] [Abstract][Full Text] [Related]
20. The third transmembrane segment of orai1 protein modulates Ca2+ release-activated Ca2+ (CRAC) channel gating and permeation properties.
Srikanth S; Yee MK; Gwack Y; Ribalet B
J Biol Chem; 2011 Oct; 286(40):35318-28. PubMed ID: 21865174
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]