Structural and functional determinants of conserved lipid interaction domains of inward rectifying Kir6.2 channels - Wikidata - awgldk - TriplyDB

Structural and functional determinants of conserved lipid interaction domains of inward rectifying Kir6.2 channels

Structural and functional determinants of conserved lipid interaction domains of inward rectifying Kir6.2 channels

http://www.wikidata.org/entity/Q36445287

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Direct and specific activation of human inward rectifier K+ channels by membrane phosphatidylinositol 4,5-bisphosphate Molecular determinants of PI(4,5)P2 and PI(3,4,5)P3 regulation of the epithelial Na+ channel Tamm-Horsfall glycoprotein interacts with renal outer medullary potassium channel ROMK2 and regulates its function Molecular basis for Kir6.2 channel inhibition by adenine nucleotides.Cholesterol sensitivity and lipid raft targeting of Kir2.1 channels.Dual-mode phospholipid regulation of human inward rectifying potassium channels N-terminal transmembrane domain of SUR1 controls gating of Kir6.2 by modulating channel sensitivity to PIP2 Muscle KATP channels: recent insights to energy sensing and myoprotection Interplay between PIP3 and calmodulin regulation of olfactory cyclic nucleotide-gated channels.Gating mechanism of KATP channels: function fits form.Phosphoinositide control of membrane protein function: a frontier led by studies on ion channels.Fourier transform coupled to tryptophan-scanning mutagenesis: lessons from its application to the prediction of secondary structure in the acetylcholine receptor lipid-exposed transmembrane domains.Phosphatidylinositol-4,5-bisphosphate, PIP2, controls KCNQ1/KCNE1 voltage-gated potassium channels: a functional homology between voltage-gated and inward rectifier K+ channels.Secondary structure and gating rearrangements of transmembrane segments in rat P2X4 receptor channels.KATP Channels in the Cardiovascular System.The role of NH2-terminal positive charges in the activity of inward rectifier KATP channels Stabilization of the activity of ATP-sensitive potassium channels by ion pairs formed between adjacent Kir6.2 subunits.Ligand-dependent linkage of the ATP site to inhibition gate closure in the KATP channel DEND mutation in Kir6.2 (KCNJ11) reveals a flexible N-terminal region critical for ATP-sensing of the KATP channel.KirBac1.1: it's an inward rectifying potassium channel.Pharmacological rescue of trafficking-impaired ATP-sensitive potassium channels.Channelopathies linked to plasma membrane phosphoinositides.Fourier transform coupled tryptophan scanning mutagenesis identifies a bending point on the lipid-exposed δM3 transmembrane domain of the Torpedo californica nicotinic acetylcholine receptor.Protein kinase-independent activation of CFTR by phosphatidylinositol phosphates.An andersen-Tawil syndrome mutation in Kir2.1 (V302M) alters the G-loop cytoplasmic K+ conduction pathway.Contribution of cytosolic cysteine residues to the gating properties of the Kir2.1 inward rectifier.Molecular determinants of cardiac K(ATP) channel activation by epoxyeicosatrienoic acids.PIP(2)-binding site in Kir channels: definition by multiscale biomolecular simulations.Tryptophan scanning mutagenesis reveals distortions in the helical structure of the δM4 transmembrane domain of the Torpedo californica nicotinic acetylcholine receptor.Identification of the PIP2-binding site on Kir6.2 by molecular modelling and functional analysis.Tryptophan-scanning mutagenesis in the alphaM3 transmembrane domain of the muscle-type acetylcholine receptor. A spring model revealed.A role for the middle C terminus of G-protein-activated inward rectifier potassium channels in regulating gating.Inward rectification by polyamines in mouse Kir2.1 channels: synergy between blocking components.Modeling transmural heterogeneity of K(ATP) current in rabbit ventricular myocytes.Functional mapping of the N-terminal arginine cluster and C-terminal acidic residues of Kir6.2 channel fused to a G protein-coupled receptor.Lipid signaling to membrane proteins: From second messengers to membrane domains and adapter-free endocytosis.Identification of a functional phosphatidylinositol 3,4,5-trisphosphate binding site in the epithelial Na+ channel.

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P2860

Structural and functional determinants of conserved lipid interaction domains of inward rectifying Kir6.2 channels

http://www.wikidata.org/entity/Q36445287

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2002 nî lūn-bûn

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2002年學術文章

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Structural and functional dete ...... ard rectifying Kir6.2 channels

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The Journal of General Physiology

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Structural and functional dete ...... ard rectifying Kir6.2 channels

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Catherine A Cukras

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Colin G Nichols

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Iana Jeliazkova

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P2860

Crystal structure of the Dbl and pleckstrin homology domains from the human Son of sevenless protein

The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

The PH domain and the polybasic c domain of cytohesin-1 cooperate specifically in plasma membrane association and cellular function

Expression of a functional Kir4 family inward rectifier K+ channel from a gene cloned from mouse liver

The solution structure and dynamics of the pleckstrin homology domain of G protein-coupled receptor kinase 2 (beta-adrenergic receptor kinase 1). A binding partner of Gbetagamma subunits

SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

Mapping of the physical interaction between the intracellular domains of an inwardly rectifying potassium channel, Kir6.2

Mutational analysis of Gbetagamma and phospholipid interaction with G protein-coupled receptor kinase 2

Phosphatidylinositol 3-kinase-dependent membrane association of the Bruton's tyrosine kinase pleckstrin homology domain visualized in single living cells

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10.1085/JGP.20028562

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