Crystal structures of the GluR5 and GluR6 ligand binding cores: molecular mechanisms underlying kainate receptor selectivity.
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Allosteric control of an ionotropic glutamate receptor with an optical switch.Kainate receptors coming of age: milestones of two decades of researchPiracetam defines a new binding site for allosteric modulators of alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) receptorsAmino acid substitutions in the pore helix of GluR6 control inhibition by membrane fatty acidsPartial agonism and antagonism of the ionotropic glutamate receptor iGLuR5: structures of the ligand-binding core in complex with domoic acid and 2-amino-3-[5-tert-butyl-3-(phosphonomethoxy)-4-isoxazolyl]propionic acidMolecular Basis of Kainate Receptor Modulation by SodiumMolecular mechanism of ligand recognition by NR3 subtype glutamate receptorsACET is a highly potent and specific kainate receptor antagonist: Characterisation and effects on hippocampal mossy fibre functionStructure of the S1S2 glutamate binding domain of GLuR3Correlating AMPA Receptor Activation and Cleft Closure across Subunits: Crystal Structures of the GluR4 Ligand-Binding Domain in Complex with Full and Partial Agonists †Full Domain Closure of the Ligand-binding Core of the Ionotropic Glutamate Receptor iGluR5 Induced by the High Affinity Agonist Dysiherbaine and the Functional Antagonist 8,9-DideoxyneodysiherbaineStability of ligand-binding domain dimer assembly controls kainate receptor desensitizationThe N-terminal domain of GluR6-subtype glutamate receptor ion channelsStructure of the zinc-bound amino-terminal domain of the NMDA receptor NR2B subunitX-ray structure, symmetry and mechanism of an AMPA-subtype glutamate receptorMolecular Mechanism of Flop Selectivity and Subsite Recognition for an AMPA Receptor Allosteric Modulator: Structures of GluA2 and GluA3 in Complexes with PEPABinding site and ligand flexibility revealed by high resolution crystal structures of GluK1 competitive antagonistsCrystal Structures of the Glutamate Receptor Ion Channel GluK3 and GluK5 Amino-Terminal DomainsMechanisms of Modal Activation of GluA3 ReceptorsMechanism of AMPA Receptor Activation by Partial Agonists: DISULFIDE TRAPPING OF CLOSED LOBE CONFORMATIONSThe Structure of (-)-Kaitocephalin Bound to the Ligand Binding Domain of the (S)- -Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid (AMPA)/Glutamate Receptor, GluA2Zinc Potentiates GluK3 Glutamate Receptor Function by Stabilizing the Ligand Binding Domain Dimer InterfaceAnions Mediate Ligand Binding in Adineta vaga Glutamate Receptor Ion ChannelsStructural Determinants of Agonist Efficacy at the Glutamate Binding Site of N-Methyl-D-Aspartate ReceptorsStructural and pharmacological characterization of phenylalanine-based AMPA receptor antagonists at kainate receptorsCorrelating efficacy and desensitization with GluK2 ligand-binding domain movementsThe Loss of an Electrostatic Contact Unique to AMPA Receptor Ligand Binding Domain 2 Slows Channel ActivationStructural Insights into Competitive Antagonism in NMDA ReceptorsMolecular recognition of two 2,4-syn-functionalized (S)-glutamate analogues by the kainate receptor GluK3 ligand binding domainActivation of NMDA receptors and the mechanism of inhibition by ifenprodil.Structural basis of kainate subtype glutamate receptor desensitization.Glutamate binding and conformational flexibility of ligand-binding domains are critical early determinants of efficient kainate receptor biogenesis.Glutamate receptor ion channels: structure, regulation, and functionOptical control of endogenous receptors and cellular excitability using targeted covalent photoswitchesVariant ionotropic glutamate receptors as chemosensory receptors in DrosophilaGlutamate receptor desensitization is mediated by changes in quaternary structure of the ligand binding domain.Structural mechanism of glutamate receptor activation and desensitization.The neurobiologist's guide to structural biology: a primer on why macromolecular structure matters and how to evaluate structural data.Novel analogs and stereoisomers of the marine toxin neodysiherbaine with specificity for kainate receptorsType II and III Taste Bud Cells Preferentially Expressed Kainate Glutamate Receptors in Rats.
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P2860
Crystal structures of the GluR5 and GluR6 ligand binding cores: molecular mechanisms underlying kainate receptor selectivity.
description
2005 nî lūn-bûn
@nan
2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Crystal structures of the GluR ...... kainate receptor selectivity.
@ast
Crystal structures of the GluR ...... kainate receptor selectivity.
@en
Crystal structures of the GluR ...... kainate receptor selectivity.
@nl
type
label
Crystal structures of the GluR ...... kainate receptor selectivity.
@ast
Crystal structures of the GluR ...... kainate receptor selectivity.
@en
Crystal structures of the GluR ...... kainate receptor selectivity.
@nl
prefLabel
Crystal structures of the GluR ...... kainate receptor selectivity.
@ast
Crystal structures of the GluR ...... kainate receptor selectivity.
@en
Crystal structures of the GluR ...... kainate receptor selectivity.
@nl
P1433
P1476
Crystal structures of the GluR ...... kainate receptor selectivity.
@en
P2093
Mark L Mayer
P304
P356
10.1016/J.NEURON.2005.01.031
P407
P577
2005-02-01T00:00:00Z