The fourth transmembrane segment of the dopamine D2 receptor: accessibility in the binding-site crevice and position in the transmembrane bundle

The fourth transmembrane segment of the dopamine D2 receptor: accessibility in the binding-site crevice and position in the transmembrane bundle

Item
http://www.wikidata.org/entity/Q28509877
Mutagenesis analysis of the serotonin 5-HT2C receptor and a Caenorhabditis elegans 5-HT2 homologue: conserved residues of helix 4 and helix 7 contribute to agonist-dependent activation of 5-HT2 receptorsEvolution-guided discovery and recoding of allosteric pathway specificity determinants in psychoactive bioamine receptors.Analysis of transmembrane domains 1 and 4 of the human angiotensin II AT1 receptor by cysteine-scanning mutagenesis.Crosstalk in G protein-coupled receptors: changes at the transmembrane homodimer interface determine activation.Homology model of the CB1 cannabinoid receptor: sites critical for nonclassical cannabinoid agonist interaction.Analysis of transmembrane segment 7 of the dipeptide transporter hPepT1 by cysteine-scanning mutagenesis.G protein-coupled receptor drug discovery: implications from the crystal structure of rhodopsin.The second extracellular loop of the dopamine D2 receptor lines the binding-site crevice.Residues accessible in the binding-site crevice of transmembrane helix 6 of the CB2 cannabinoid receptorThe predicted 3D structure of the human D2 dopamine receptor and the binding site and binding affinities for agonists and antagonists.Role of the transmembrane domain 4/extracellular loop 2 junction of the human gonadotropin-releasing hormone receptor in ligand binding and receptor conformational selection.Impact of D2 receptor internalization on binding affinity of neuroimaging radiotracers.Allosteric communication between protomers of dopamine class A GPCR dimers modulates activation.Differential helical orientations among related G protein-coupled receptors provide a novel mechanism for selectivity. Studies with salvinorin A and the kappa-opioid receptor.1-Methylpyridinium-4-(4-phenylmethanethiosulfonate) iodide, MTS-MPP+, a novel scanning cysteine accessibility method (SCAM) reagent for monoamine transporter studies.GABA(A) receptor beta 2 Tyr97 and Leu99 line the GABA-binding site. Insights into mechanisms of agonist and antagonist actions.Rigid nonproteinogenic cyclic amino acids as ligands for glutamate receptors: trans-tris(homoglutamic) acids.
P2860

The fourth transmembrane segment of the dopamine D2 receptor: accessibility in the binding-site crevice and position in the transmembrane bundle

Item
http://www.wikidata.org/entity/Q28509877
description
2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2000
@ast
im Oktober 2000 veröffentlicher wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2000/10/10)
@sk
vědecký článek publikovaný v roce 2000
@cs
wetenschappelijk artikel (gepubliceerd op 2000/10/10)
@nl
наукова стаття, опублікована в жовтні 2000
@uk
مقالة علمية (نشرت في 10-10-2000)
@ar
name
The fourth transmembrane segme ...... on in the transmembrane bundle
@ast
The fourth transmembrane segme ...... on in the transmembrane bundle
@en
The fourth transmembrane segme ...... on in the transmembrane bundle
@nl
type
label
The fourth transmembrane segme ...... on in the transmembrane bundle
@ast
The fourth transmembrane segme ...... on in the transmembrane bundle
@en
The fourth transmembrane segme ...... on in the transmembrane bundle
@nl
prefLabel
The fourth transmembrane segme ...... on in the transmembrane bundle
@ast
The fourth transmembrane segme ...... on in the transmembrane bundle
@en
The fourth transmembrane segme ...... on in the transmembrane bundle
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P356
P1433
P1476
The fourth transmembrane segme ...... on in the transmembrane bundle
@en
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921