Phosphoinositide-mediated gating of inwardly rectifying K(+) channels. - Wikidata - awgldk - TriplyDB

Phosphoinositide-mediated gating of inwardly rectifying K(+) channels.

Phosphoinositide-mediated gating of inwardly rectifying K(+) channels.

http://www.wikidata.org/entity/Q36829579

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Structural basis of PIP2 activation of the classical inward rectifier K+ channel Kir2.2 Neural KCNQ (Kv7) channels How highly charged anionic lipids bind and regulate ion channels A Structural Determinant for the Control of PIP2 Sensitivity in G Protein-gated Inward Rectifier K+ Channels Identification of yeast proteins necessary for cell-surface function of a potassium channel.Phosphoinositides: lipid regulators of membrane proteins A dual polybasic motif determines phosphoinositide binding and regulation in the P2X channel family Cholesterol binding to ion channels Lipids driving protein structure? Evolutionary adaptations in Kir channels Regulation of ion channel function by the host lipid bilayer examined by a stopped-flow spectrofluorometric assay.A novel mitochondrial K(ATP) channel assay.State-dependent network connectivity determines gating in a K+ channel Phosphatidylinositol 4,5-bisphosphate activates Slo3 currents and its hydrolysis underlies the epidermal growth factor-induced current inhibition Flecainide increases Kir2.1 currents by interacting with cysteine 311, decreasing the polyamine-induced rectification Specific residues of the cytoplasmic domains of cardiac inward rectifier potassium channels are effective antifibrillatory targets.Gating of transient receptor potential melastatin 8 (TRPM8) channels activated by cold and chemical agonists in planar lipid bilayers.Gating of a G protein-sensitive mammalian Kir3.1 prokaryotic Kir channel chimera in planar lipid bilayers Structural dynamics of potassium-channel gating revealed by single-molecule FRET.Interplay Between Lipid Modulators of Kir2 Channels: Cholesterol and PIP2.Structural bases for the different anti-fibrillatory effects of chloroquine and quinidine.N-terminal transmembrane domain of SUR1 controls gating of Kir6.2 by modulating channel sensitivity to PIP2 Snowflake vitreoretinal degeneration (SVD) mutation R162W provides new insights into Kir7.1 ion channel structure and function Genetic defects in the hotspot of inwardly rectifying K(+) (Kir) channels and their metabolic consequences: a review Identification of the Conformational transition pathway in PIP2 Opening Kir Channels.Phosphatidylinositol-4,5-bisphosphate regulates epidermal growth factor receptor activation Phosphoinositide control of membrane protein function: a frontier led by studies on ion channels.Mutations in Nature Conferred a High Affinity Phosphatidylinositol 4,5-Bisphosphate-binding Site in Vertebrate Inwardly Rectifying Potassium Channels The molecular mechanism by which PIP(2) opens the intracellular G-loop gate of a Kir3.1 channel.Metabolic and thermal stimuli control K(2P)2.1 (TREK-1) through modular sensory and gating domains.A Quantitative Model of the GIRK1/2 Channel Reveals That Its Basal and Evoked Activities Are Controlled by Unequal Stoichiometry of Gα and Gβγ.Inhibition of inwardly rectifying Kir2.x channels by the novel anti-cancer agent gambogic acid depends on both pore block and PIP2 interference.Distant cytosolic residues mediate a two-way molecular switch that controls the modulation of inwardly rectifying potassium (Kir) channels by cholesterol and phosphatidylinositol 4,5-bisphosphate (PI(4,5)P(2)).The cytosolic GH loop regulates the phosphatidylinositol 4,5-bisphosphate-induced gating kinetics of Kir2 channels.Regulation of Ca(V)2 calcium channels by G protein coupled receptors.Diverse Kir modulators act in close proximity to residues implicated in phosphoinositide binding.A carboxy-terminal inter-helix linker as the site of phosphatidylinositol 4,5-bisphosphate action on Kv7 (M-type) K+ channels.Plasticity of postsynaptic, but not presynaptic, GABAB receptors in SSADH deficient mice.Kv7.1 (KCNQ1) properties and channelopathies.Regulation of neural KCNQ channels: signalling pathways, structural motifs and functional implications.The Molecular Mechanism of Opening the Helix Bundle Crossing (HBC) Gate of a Kir Channel.

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P2860

Phosphoinositide-mediated gating of inwardly rectifying K(+) channels.

http://www.wikidata.org/entity/Q36829579

description

2007 nî lūn-bûn

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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2007年论文

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2007年论文

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name

Phosphoinositide-mediated gating of inwardly rectifying K(+) channels.

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Phosphoinositide-mediated gating of inwardly rectifying K(+) channels.

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Phosphoinositide-mediated gating of inwardly rectifying K(+) channels.

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Pfluegers Archiv

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Phosphoinositide-mediated gating of inwardly rectifying K(+) channels.

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P2093

Avia Rosenhouse-Dantsker

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Diomedes E Logothetis

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Dmitry Lupyan

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Taihao Jin

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P2860

Cloning and functional expression of an inwardly rectifying K+ channel from human atrium

The intrinsic gating of inward rectifier K+ channels expressed from the murine IRK1 gene depends on voltage, K+ and Mg2+

A potential- and time-dependent blockade of inward rectification in frog skeletal muscle fibres by barium and strontium ions.

Gating mechanism of the cloned inward rectifier potassium channel from mouse heart.

Slow changes in potassium permeability in skeletal muscle.

Voltage-dependent activation of the inward-rectifier potassium channel in the ventricular cell membrane of guinea-pig heart.

Structural determinants and specificities for ROMK1-phosphoinositide interaction.

Targeted disruption of Kir2.1 and Kir2.2 genes reveals the essential role of the inwardly rectifying K(+) current in K(+)-mediated vasodilation.

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s00424-007-0276-5

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83-95

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10.1007/S00424-007-0276-5

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1

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