内向整流钾通道的“内核” - Suppr

Suppr

超能文献

The 'inner core' of inwardly rectifying K+ channels.

作者信息

Nichols C G

机构信息

Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, MO 63110.

出版信息

Trends Pharmacol Sci. 1993 Sep;14(9):320-3. doi: 10.1016/0165-6147(93)90003-3.

DOI:10.1016/0165-6147(93)90003-3

PMID:8249152

Abstract

摘要

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The 'inner core' of inwardly rectifying K+ channels.内向整流钾通道的“内核”

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引用本文的文献

Ammonium ions induce inactivation of Kir2.1 potassium channels expressed in Xenopus oocytes.铵离子可诱导非洲爪蟾卵母细胞中表达的Kir2.1钾通道失活。

J Physiol. 2001 Sep 1;535(Pt 2):359-70. doi: 10.1111/j.1469-7793.2001.00359.x.

[K+] dependence of open-channel conductance in cloned inward rectifier potassium channels (IRK1, Kir2.1).克隆的内向整流钾通道（IRK1、Kir2.1）中开放通道电导对[K⁺]的依赖性

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A unique P-region residue is required for slow voltage-dependent gating of a G protein-activated inward rectifier K+ channel expressed in Xenopus oocytes.非洲爪蟾卵母细胞中表达的一种G蛋白激活内向整流钾通道的缓慢电压依赖性门控需要一个独特的P区残基。

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A single aspartate residue is involved in both intrinsic gating and blockage by Mg2+ of the inward rectifier, IRK1.单个天冬氨酸残基参与内向整流钾通道IRK1的内在门控和Mg2+介导的阻断过程。

J Physiol. 1994 Jul 1;478 ( Pt 1)(Pt 1):1-6. doi: 10.1113/jphysiol.1994.sp020225.

Reversal of rectification and alteration of selectivity and pharmacology in a mammalian Kv1.1 potassium channel by deletion of domains S1 to S4.通过缺失S1至S4结构域逆转哺乳动物Kv1.1钾通道的整流、选择性改变及药理学特性

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