Orthosteric and allosteric binding sites of P2X receptors
about
Molecular and functional properties of P2X receptors--recent progress and persisting challengesExploring the ATP-binding site of P2X receptorsInsights into the Molecular Mechanisms Underlying Mammalian P2X7 Receptor Functions and Contributions in Diseases, Revealed by Structural Modeling and Single Nucleotide PolymorphismsA P2X receptor from the tardigrade species Hypsibius dujardini with fast kinetics and sensitivity to zinc and copper.P2X receptors: dawn of the post-structure era.Gated access to the pore of a P2X receptor: structural implications for closed-open transitions.A putative extracellular salt bridge at the subunit interface contributes to the ion channel function of the ATP-gated P2X2 receptorCovalent modification of mutant rat P2X2 receptors with a thiol-reactive fluorophore allows channel activation by zinc or acidic pH without ATP.Structural insights into the function of P2X4: an ATP-gated cation channel of neuroendocrine cells.Activation and regulation of purinergic P2X receptor channelsInherent dynamics of head domain correlates with ATP-recognition of P2X4 receptors: insights gained from molecular simulations.Allosteric modulation of purine and pyrimidine receptors.Allosteric nature of P2X receptor activation probed by photoaffinity labelling.Allosteric modulation of ATP-gated P2X receptor channelsGating the pore of P2X receptor channelsProteomics to identify proteins interacting with P2X2 ligand-gated cation channels.Structural interpretation of P2X receptor mutagenesis studies on drug actionHeteromeric assembly of P2X subunits.Key sites for P2X receptor function and multimerization: overview of mutagenesis studies on a structural basis.Carbon monoxide is a rapid modulator of recombinant and native P2X(2) ligand-gated ion channels.Characterisation of ATP analogues to cross-link and label P2X receptorsRegulation of Pannexin 1 Surface Expression by Extracellular ATP: Potential Implications for Nervous System Function in Health and Disease.Contribution of the region Glu181 to Val200 of the extracellular loop of the human P2X1 receptor to agonist binding and gating revealed using cysteine scanning mutagenesis.Characterisation of the R276A gain-of-function mutation in the ectodomain of murine P2X7Amino acid residues constituting the agonist binding site of the human P2X3 receptorActivation of the P2X7 ion channel by soluble and covalently bound ligands.A conformation and charge co-modulated ultrasensitive biomimetic ion channel.
P2860
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P2860
Orthosteric and allosteric binding sites of P2X receptors
description
2009 nî lūn-bûn
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2009 թուականի Մարտին հրատարակուած գիտական յօդուած
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2009 թվականի մարտին հրատարակված գիտական հոդված
@hy
2009年の論文
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2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Orthosteric and allosteric binding sites of P2X receptors
@ast
Orthosteric and allosteric binding sites of P2X receptors
@en
Orthosteric and allosteric binding sites of P2X receptors
@nl
type
label
Orthosteric and allosteric binding sites of P2X receptors
@ast
Orthosteric and allosteric binding sites of P2X receptors
@en
Orthosteric and allosteric binding sites of P2X receptors
@nl
prefLabel
Orthosteric and allosteric binding sites of P2X receptors
@ast
Orthosteric and allosteric binding sites of P2X receptors
@en
Orthosteric and allosteric binding sites of P2X receptors
@nl
P2860
P1476
Orthosteric and allosteric binding sites of P2X receptors
@en
P2093
P2860
P2888
P304
P356
10.1007/S00249-008-0275-2
P407
P577
2009-03-01T00:00:00Z