Size of side-chain at channel pore mouth affects Ca(2+) block of P2X(2) receptor

scientific article published in August 2002

Size of side-chain at channel pore mouth affects Ca(2+) block of P2X(2) receptor is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/S0014-2999(02)02001-0
P698PubMed publication ID12167461

P2093author name stringKen Nakazawa
Yasuo Ohno
Reiko Ishii-Nozawa
Koichi Takeuchi
Hideaki Sawa
Hiloe Ojima
P2860cites workPolar residues of the second transmembrane domain influence cation permeability of the ATP-gated P2X(2) receptorQ28201447
Pharmacology of cloned P2X receptorsQ33932194
Molecular physiology of P2X receptors and ATP signalling at synapsesQ34188163
New structural motif for ligand-gated ion channels defined by an ionotropic ATP receptorQ34292603
Block by calcium of ATP-activated channels in pheochromocytoma cellsQ36411351
On the contribution of the first transmembrane domain to whole-cell current through an ATP-gated ionotropic P2X receptor.Q40788207
Amino acid residues involved in gating identified in the first membrane-spanning domain of the rat P2X(2) receptorQ40816581
The past, present and future of purine nucleotides as signalling moleculesQ40878144
Inactivation of P2X2 purinoceptors by divalent cationsQ40905705
Ion permeation and block of P2X(2) purinoceptors: single channel recordingsQ40916730
Pore dilation of neuronal P2X receptor channelsQ40960421
Identification of amino acid residues contributing to the pore of a P2X receptorQ41106961
A monovalent cationic conductance that is blocked by extracellular divalent cations in Xenopus oocytesQ46868292
An asparagine residue regulating conductance through P2X2 receptor/channelsQ47894113
The ion selectivity of a membrane conductance inactivated by extracellular calcium in Xenopus oocytesQ48938763
An aspartic acid residue near the second transmembrane segment of ATP receptor/channel regulates agonist sensitivityQ48944134
Potent inhibition by trivalent cations of ATP-gated channelsQ48958734
Dopamine and 5-hydroxytryptamine selectively potentiate neuronal type ATP receptor channelsQ49021782
Structural invariants in protein foldingQ59064399
Block by extracellular Mg2+ of single human purinergic P2X4 receptor channels expressed in human embryonic kidney cellsQ73477424
A domain contributing to the ion channel of ATP-gated P2X2 receptors identified by the substituted cysteine accessibility methodQ74315052
P433issue3
P407language of work or nameEnglishQ1860
P304page(s)207-211
P577publication date2002-08-01
P1433published inEuropean Journal of PharmacologyQ1376712
P1476titleSize of side-chain at channel pore mouth affects Ca(2+) block of P2X(2) receptor
P478volume449

Reverse relations

cites work (P2860)
Q34313783Pore-opening mechanism in trimeric P2X receptor channels
Q35587851Roles of the lateral fenestration residues of the P2X₄ receptor that contribute to the channel function and the deactivation effect of ivermectin

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