The Concerted Contribution of the S4-S5 Linker and the S6 Segment to the Modulation of a Kv Channel by 1-Alkanols-Reference-Cited by-同舟云学术

The Concerted Contribution of the S4-S5 Linker and the S6 Segment to the Modulation of a Kv Channel by 1-Alkanols

Published:2006-08-03 Issue:5 Volume:70 Page:1542-1554
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Bhattacharji Aditya,Kaplan Benjamin,Harris Thanawath,Qu Xiaoguang,Germann Markus W.,Covarrubias Manuel

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference39 articles.

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4. Covarrubias M, Bhattacharji A, Harris T, Kaplan B, and Germann MW (2005) Alcohol and anesthetic action at the gate of a voltage-dependent K+ channel, in Basic and Systemic Mechanisms of Anesthesia (Mashimo T, Ogli K, and Uchida I eds) pp 55-60, Elsevier B.V., Amsterdam.

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1. Capturing the Molecular Mechanism of Anesthetic Action by Simulation Methods;Chemical Reviews;2018-10-25

2. Gambierol and n-alkanols inhibit Shaker Kv channel via distinct binding sites outside the K+ pore;Toxicon;2016-09

3. Voltage-sensor conformation shapes the intra-membrane drug binding site that determines gambierol affinity in Kv channels;Neuropharmacology;2016-08

4. The residue I257 at S4–S5 linker in KCNQ1 determines KCNQ1/KCNE1 channel sensitivity to 1-alkanols;Acta Pharmacologica Sinica;2016-01

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