Chloride channels of glycine and GABA receptors with blockers: Monte Carlo minimization and structure-activity relationships.
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Comparison of crystal structures of human androgen receptor ligand-binding domain complexed with various agonists reveals molecular determinants responsible for binding affinityThe dual modulatory effects of efavirenz on GABAA receptors are mediated via two distinct sites.Monte Carlo-energy minimization of correolide in the Kv1.3 channel: possible role of potassium ion in ligand-receptor interactions.Docking flexible ligands in proteins with a solvent exposure- and distance-dependent dielectric function.KvAP-based model of the pore region of shaker potassium channel is consistent with cadmium- and ligand-binding experimentsStructural model for gamma-aminobutyric acid receptor noncompetitive antagonist binding: widely diverse structures fit the same siteMapping convulsants' binding to the GABA-A receptor chloride ionophore: a proposed model for channel binding sites.Mixed antagonistic effects of the ginkgolides at recombinant human ρ1 GABAC receptorsDifferential distribution of glycine receptor subtypes at the rat calyx of Held synapse.Stoichiometric pore mutations of the GABAAR reveal a pattern of hydrogen bonding with picrotoxin.Discriminating between 5-HT₃A and 5-HT₃AB receptorsGlycine receptors in a population of adult mammalian cones.Electrophysiological Signature of Homomeric and Heteromeric Glycine Receptor Channels.Modeling noncompetitive antagonism of a nicotinic acetylcholine receptor.Modeling P-loops domain of sodium channel: homology with potassium channels and interaction with ligands.Isolation of an Escherichia coli K4 kfoC mutant over-producing capsular chondroitin.Molecular determinants of the regioselectivity of toluene/o-xylene monooxygenase from Pseudomonas sp. strain OX1Acidic residues on the voltage-sensor domain determine the activation of the NaChBac sodium channel.Mechanisms for picrotoxinin and picrotin blocks of alpha2 homomeric glycine receptors.Y1767C, a novel SCN5A mutation, induces a persistent Na+ current and potentiates ranolazine inhibition of Nav1.5 channels.Identification of a novel residue within the second transmembrane domain that confers use-facilitated block by picrotoxin in glycine alpha 1 receptors.Cloning and functional characterization of two glycine receptor alpha-subunits from the perch retina.Terpene trilactones from Ginkgo biloba are antagonists of cortical glycine and GABA(A) receptors.Sodium channel activators: model of binding inside the pore and a possible mechanism of action.A picrotoxin-specific conformational change in the glycine receptor M2-M3 loop.Side chain flexibility and the pore dimensions in the GABAA receptor.Stoichiometry of a pore mutation that abolishes picrotoxin-mediated antagonism of the GABAA receptor.
P2860
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P2860
Chloride channels of glycine and GABA receptors with blockers: Monte Carlo minimization and structure-activity relationships.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
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2000年學術文章
@zh-hant
name
Chloride channels of glycine a ...... ucture-activity relationships.
@en
type
label
Chloride channels of glycine a ...... ucture-activity relationships.
@en
prefLabel
Chloride channels of glycine a ...... ucture-activity relationships.
@en
P2860
P1433
P1476
Chloride channels of glycine a ...... ucture-activity relationships.
@en
P2093
Bregestovski PD
P2860
P304
P356
10.1016/S0006-3495(00)76729-4
P407
P577
2000-04-01T00:00:00Z