A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
about
Zinc as Allosteric Ion Channel Modulator: Ionotropic Receptors as MetalloproteinsTwo gamma2L subunit domains confer low Zn2+ sensitivity to ternary GABA(A) receptorsFunctional role of polar amino acid residues in Na+/H+ exchangersConditionally and transiently disordered proteins: awakening cryptic disorder to regulate protein function.Carbonic anhydrase I, II, and VI, blood plasma, erythrocyte and saliva zinc and copper increase after repetitive transcranial magnetic stimulation.Electrophysiological evidence of GABAA and GABAC receptors on zebrafish retinal bipolar cellsGABArho 1/GABAAalpha 1 receptor chimeras to study receptor desensitization.Allosteric modulation of retinal GABA receptors by ascorbic acid.Zinc-permeable ion channels: effects on intracellular zinc dynamics and potential physiological/pathophysiological significance.Identification of a specific region in the e1 fusion protein involved in zinc inhibition of semliki forest virus fusion.pH-responsive titratable inotropic performance of histidine-modified cardiac troponin I.Dopamine and serotonin modulate human GABAρ1 receptors expressed in Xenopus laevis oocytes.Effects of Zn2+ on wild and mutant neuronal alpha7 nicotinic receptors.GABA-ρ receptors: distinctive functions and molecular pharmacology.Histidines are responsible for zinc potentiation of the current in KDC1 carrot channels.An N-terminal histidine regulates Zn(2+) inhibition on the murine GABA(A) receptor beta3 subunitKinetic and mutational analysis of Zn2+ modulation of recombinant human inhibitory glycine receptors.Identification of an inhibitory Zn2+ binding site on the human glycine receptor alpha1 subunit.Evidence for phosphorylation-dependent internalization of recombinant human rho1 GABAC receptors.Zn2+ inhibition of recombinant GABAA receptors: an allosteric, state-dependent mechanism determined by the gamma-subunit.Delineation of an endogenous zinc-binding site in the human dopamine transporter.Zinc inactivates melastatin transient receptor potential 2 channels via the outer pore.The role of histidine residues in modulation of the rat P2X(2) purinoceptor by zinc and pH.
P2860
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P2860
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
description
1995 nî lūn-bûn
@nan
1995 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@ast
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@en
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@nl
type
label
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@ast
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@en
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@nl
prefLabel
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@ast
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@en
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@nl
P2093
P3181
P1476
A single histidine residue is essential for zinc inhibition of GABA rho 1 receptors
@en
P2093
P304
P3181
P356
10.1523/JNEUROSCI.15-11-07684.1995
P407
P577
1995-11-01T00:00:00Z