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Summary Anatomy Item Literature (4897) Expression Attributions Wiki
XB-ANAT-3713

Papers associated with left (and p2rx1)

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Mapping the binding site of the P2X receptor antagonist PPADS reveals the importance of orthosteric site charge and the cysteine-rich head region., Huo H., J Biol Chem. August 17, 2018; 293 (33): 12820-12831.                

Cysteine scanning mutagenesis (residues Glu52-Gly96) of the human P2X1 receptor for ATP: mapping agonist binding and channel gating., Allsopp RC., J Biol Chem. August 19, 2011; 286 (33): 29207-17.              

Contribution of the intracellular C terminal domain to regulation of human P2X1 receptors for ATP by phorbol ester and Gq coupled mGlu(1α) receptors., Wen H., Eur J Pharmacol. March 5, 2011; 654 (2): 155-9.        

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., Roberts JA., J Neurochem. May 1, 2009; 109 (4): 1042-52.              

Regions of the amino terminus of the P2X receptor required for modification by phorbol ester and mGluR1alpha receptors., Wen H., J Neurochem. January 1, 2009; 108 (2): 331-40.            

Lack of evidence for direct phosphorylation of recombinantly expressed P2X(2) and P2X (3) receptors by protein kinase C., Franklin C., Purinergic Signal. September 1, 2007; 3 (4): 377-88.              

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