Characterisation of ATP analogues to cross-link and label P2X receptors
about
Exploring the ATP-binding site of P2X receptorsEvidence for shear-mediated Ca2+ entry through mechanosensitive cation channels in human platelets and a megakaryocytic cell line.Allosteric nature of P2X receptor activation probed by photoaffinity labelling.Ligand-gated purinergic receptors regulate HIV-1 Tat and morphine related neurotoxicity in primary mouse striatal neuron-glia co-cultures.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.Conformational flexibility of the agonist binding jaw of the human P2X3 receptor is a prerequisite for channel opening.Mass spectrometry analysis of human P2X1 receptors; insight into phosphorylation, modelling and conformational changes.P2X receptor intermediate activation states have altered nucleotide selectivity.
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P2860
Characterisation of ATP analogues to cross-link and label P2X receptors
description
2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年學術文章
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2008年學術文章
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2008年學術文章
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name
Characterisation of ATP analogues to cross-link and label P2X receptors
@en
Characterisation of ATP analogues to cross-link and label P2X receptors.
@nl
type
label
Characterisation of ATP analogues to cross-link and label P2X receptors
@en
Characterisation of ATP analogues to cross-link and label P2X receptors.
@nl
prefLabel
Characterisation of ATP analogues to cross-link and label P2X receptors
@en
Characterisation of ATP analogues to cross-link and label P2X receptors.
@nl
P2093
P2860
P1433
P1476
Characterisation of ATP analogues to cross-link and label P2X receptors
@en
P2093
Andrew J Powell
Kelvin C Agboh
Richard J Evans
P2860
P304
P356
10.1016/J.NEUROPHARM.2008.05.018
P577
2008-07-02T00:00:00Z