An Intersubunit Zinc Binding Site in Rat P2X2 Receptors
Open Access
- 1 July 2005
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 280 (28) , 25982-25993
- https://doi.org/10.1074/jbc.m504545200
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Molecular Determinants of the Agonist Binding Domain of a P2X Receptor ChannelMolecular Pharmacology, 2005
- Molecular properties of ATP-gated P2X receptor ion channelsTrends in Pharmacological Sciences, 2004
- ATP Binding at Human P2X1 ReceptorsJournal of Biological Chemistry, 2004
- Insights into the Structural Basis for Zinc Inhibition of the Glycine ReceptorJournal of Biological Chemistry, 2003
- Monomeric and Dimeric Byproducts are the Principal Functional Elements of Higher Order P2X1 ConcatamersMolecular Pharmacology, 2003
- The role of histidine residues in modulation of the rat P2X2 purinoceptor by zinc and pHThe Journal of Physiology, 2002
- Identification of Amino Acid Residues Contributing to the ATP-binding Site of a Purinergic P2X ReceptorJournal of Biological Chemistry, 2000
- The Role of Positively Charged Amino Acids in ATP Recognition by Human P2X1 ReceptorsJournal of Biological Chemistry, 2000
- Zn2+ modulation of ATP‐responses at recombinant P2X2 receptors and its dependence on extracellular pHBritish Journal of Pharmacology, 1998
- Two mechanisms for inward rectification of current flow through the purinoceptor P2X2 class of ATP‐gated channelsThe Journal of Physiology, 1998