RNA editing modulates the binding of drugs and highly unsaturated fatty acids to the open pore of Kv potassium channels. - Wikidata - wikimedia - TriplyDB

RNA editing modulates the binding of drugs and highly unsaturated fatty acids to the open pore of Kv potassium channels.

RNA editing modulates the binding of drugs and highly unsaturated fatty acids to the open pore of Kv potassium channels.

http://www.wikidata.org/entity/Q42165768

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Regulation of Ion Channel and Transporter Function Through RNA Editing Identification of putative potassium channel homologues in pathogenic protozoa K(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy.Transcript diversification in the nervous system: a to I RNA editing in CNS function and disease development Mutations underlying Episodic Ataxia type-1 antagonize Kv1.1 RNA editing Editing of neurotransmitter receptor and ion channel RNAs in the nervous system RNA editing in the central cavity as a mechanism to regulate surface expression of the voltage-gated potassium channel Kv1.1.Editing of human K(V)1.1 channel mRNAs disrupts binding of the N-terminus tip at the intracellular cavity.The Molecular Basis of Polyunsaturated Fatty Acid Interactions with the Shaker Voltage-Gated Potassium Channel Homology model and targeted mutagenesis identify critical residues for arachidonic acid inhibition of Kv4 channels A-to-I RNA editing: effects on proteins key to neural excitability Q/R site interactions with the M3 helix in GluK2 kainate receptor channels revealed by thermodynamic mutant cycles.The ADAR RNA editing enzyme controls neuronal excitability in Drosophila melanogaster.Actions and Mechanisms of Polyunsaturated Fatty Acids on Voltage-Gated Ion Channels.Polyunsaturated Fatty acids modify the gating of kv channels Mechanism of electromechanical coupling in voltage-gated potassium channels.Putative impact of RNA editing on drug discovery.An electrostatic potassium channel opener targeting the final voltage sensor transition.Characterizing the fatty acid binding site in the cavity of potassium channel KcsA Multiple binding sites for fatty acids on the potassium channel KcsA Channels get in an HUFA: RNA editing gets them out of a jam.RNA editing of Kv1.1 channels may account for reduced ictogenic potential of 4-aminopyridine in chronic epileptic rats.Modulation of thalamocortical oscillations by TRIP8b, an auxiliary subunit for HCN channels.Kv1.5 blockers preferentially inhibit TASK-1 channels: TASK-1 as a target against atrial fibrillation and obstructive sleep apnea?Visualizing adenosine-to-inosine RNA editing in the Drosophila nervous system.

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RNA editing modulates the binding of drugs and highly unsaturated fatty acids to the open pore of Kv potassium channels.

http://www.wikidata.org/entity/Q42165768

description

2010 nî lūn-bûn

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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2010年论文

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2010年论文

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name

RNA editing modulates the bind ...... pore of Kv potassium channels.

@en

RNA editing modulates the bind ...... pore of Kv potassium channels.

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type

label

RNA editing modulates the bind ...... pore of Kv potassium channels.

@en

RNA editing modulates the bind ...... pore of Kv potassium channels.

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prefLabel

RNA editing modulates the bind ...... pore of Kv potassium channels.

@en

RNA editing modulates the bind ...... pore of Kv potassium channels.

@nl

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The EMBO Journal

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RNA editing modulates the bind ...... pore of Kv potassium channels

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Anne K Streit

http://www.w3.org/2001/XMLSchema#string

Annemarie Köhler

http://www.w3.org/2001/XMLSchema#string

Gerhard Klebe

http://www.w3.org/2001/XMLSchema#string

Günter Schlichthörl

http://www.w3.org/2001/XMLSchema#string

Jürgen Daut

http://www.w3.org/2001/XMLSchema#string

Markus Rapedius

http://www.w3.org/2001/XMLSchema#string

Michael F Netter

http://www.w3.org/2001/XMLSchema#string

Petra Ehling

http://www.w3.org/2001/XMLSchema#string

Regina Preisig-Müller

http://www.w3.org/2001/XMLSchema#string

Ricardo A Navarro-Polanco

http://www.w3.org/2001/XMLSchema#string

P2860

External blockade of the major cardiac delayed-rectifier K+ channel (Kv1.5) by polyunsaturated fatty acids

Potassium channel receptor site for the inactivation gate and quaternary amine inhibitors

Nervous system targets of RNA editing identified by comparative genomics

Novel docosanoids inhibit brain ischemia-reperfusion-mediated leukocyte infiltration and pro-inflammatory gene expression

Control of human potassium channel inactivation by editing of a small mRNA hairpin

Arachidonic acid as a bioactive molecule

Inactivation properties of voltage-gated K+ channels altered by presence of beta-subunit

The moving parts of voltage-gated ion channels.

Overlap between the ligand recognition properties of the anandamide transporter and the VR1 vanilloid receptor: inhibitors of anandamide uptake with negligible capsaicin-like activity.

Kv1.3-blocking 5-phenylalkoxypsoralens: a new class of immunomodulators.

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2101-2113

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10.1038/EMBOJ.2010.88

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13

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29

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44590768

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20461057

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