Ligand Selectivity of D2 Dopamine Receptors Is Modulated by Changes in Local Dynamics Produced by Sodium Binding (original) (raw)

Modeling and Mutational Analysis of a Putative Sodium-Binding Pocket on the Dopamine D2Receptor

Val Watts

Molecular Pharmacology, 2001

View PDFchevron_right

Induced Effects of Sodium Ions on Dopaminergic G-Protein Coupled Receptors

Jana Selent

PLoS Computational Biology, 2010

View PDFchevron_right

Serine mutations in transmembrane V of the dopamine D1 receptor affect ligand interactions and receptor activation

Robert MacKenzie

Journal of Biological Chemistry, 1992

View PDFchevron_right

Receptor Conformations Involved in Dopamine D2L Receptor Functional Selectivity Induced by Selected Transmembrane-5 Serine Mutations

Richard Mailman

Molecular Pharmacology, 2012

View PDFchevron_right

A theoretical study to investigate D2DAR/D4DAR selectivity: receptor modeling and molecular docking of dopaminergic ligands

Tiziano Tuccinardi

Journal of medicinal …, 2006

View PDFchevron_right

Universality of the Sodium Ion Binding Mechanism in Class A G-Protein-Coupled Receptors

Zahra Shamsi

Angewandte Chemie, 2018

View PDFchevron_right

Three amino acids in the D 2 dopamine receptor regulate selective ligand function and affinity

Spencer S Ericksen

Journal of Neurochemistry, 2009

View PDFchevron_right

Sodium Ion Binding Pocket Mutations and Adenosine A2AReceptor Function

Lizi Xia

Molecular Pharmacology, 2014

View PDFchevron_right

An aspartate conserved among G-protein receptors confers allosteric regulation of alpha 2-adrenergic receptors by sodium

Debra Horstman

Journal of Biological Chemistry, 1990

View PDFchevron_right

Investigation of D2Receptor-Agonist Interactions Using a Combination of Pharmacophore and Receptor Homology Modeling

Marcus Malo

ChemMedChem, 2012

View PDFchevron_right

Homology Modeling of the Dopamine D2 Receptor and Its Testing by Docking of Agonists and Tricyclic Antagonists

Curtiss Durand, Mark Froimowitz

Journal of Medicinal Chemistry, 1994

View PDFchevron_right

Molecular dynamics of dopamine at the D2 receptor

Ingebrigt Sylte

Proceedings of the National Academy of Sciences, 1991

View PDFchevron_right

The Role of a Sodium Ion Binding Site in the Allosteric Modulation of the A2A Adenosine G Protein-Coupled Receptor

David Rodríguez

Structure, 2013

View PDFchevron_right

Ligand with Two Modes of Interaction with the Dopamine D2 Receptor–An Induced-Fit Mechanism of Insurmountable Antagonism

Kristoffer Sahlholm

ACS Chemical Neuroscience

View PDFchevron_right

Hydrophobic Residues of the D2 Dopamine Receptor Are Important for Binding and Signal Transduction

Huda Akil

Journal of Neurochemistry, 2002

View PDFchevron_right

A Single Glycine in Extracellular Loop 1 Is the Critical Determinant for Pharmacological Specificity of Dopamine D2 and D3 Receptors

Thijs Beuming

Molecular Pharmacology, 2013

View PDFchevron_right

Complete Conversion of Brain D 2 Dopamine Receptors from the High to the Low-Affinity State for Dopamine Agonists, Using Sodium Ions and Guanine Nucleotide

Dimitri Grigoriadis

Journal of Neurochemistry, 1985

View PDFchevron_right

D2/D3 Dopamine Receptor Heterodimers Exhibit Unique Functional Properties

ridwan nm

Journal of Biological Chemistry, 2001

View PDFchevron_right

Dopamine D2 Receptor Agonist Binding Kinetics—Role of a Conserved Serine Residue

Kristoffer Sahlholm

2021

View PDFchevron_right

Electrostatic and Aromatic Microdomains within the Binding-Site Crevice of the D2 Receptor: Contributions of the Second Membrane-Spanning Segment

Juan C Sierra Ballesteros

Biochemistry, 1999

View PDFchevron_right

Selectivity and activation of dopamine D3R from molecular dynamics

Zohreh Fallah

View PDFchevron_right

Agonist-specific voltage sensitivity at the dopamine D 2S receptor – Molecular determinants and relevance to therapeutic ligands

Maricel Gomez

Neuropharmacology, 2011

View PDFchevron_right

Ceresa, B.P. & Limbird, L.E. Mutation of an aspartate residue highly conserved among G-protein-coupled receptors results in nonreciprocal disruption of 2-adrenergic receptor−G-protein interactions. A negative charge at amino acid residue 79 forecasts 2A-adrenergic receptor sensitivity to alloster...

Lee Limbird

Journal of Biological Chemistry

View PDFchevron_right

Modulation of agonist binding to recombinant human α2-adrenoceptors by sodium ions

Mika Scheinin

Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1998

View PDFchevron_right

Energetics of glutamate receptor ligand binding domain dimer assembly are modulated by allosteric ions

Charu Chaudhry

Proceedings of the National Academy of Sciences, 2009

View PDFchevron_right

Delineation of the Structural Basis for the Activation Properties of the Dopamine D1 Receptor Subtypes

Mario Tiberi

Journal of Biological Chemistry, 1999

View PDFchevron_right

The 2.1 Å Resolution Structure of Cyanopindolol-Bound β1-Adrenoceptor Identifies an Intramembrane Na+ Ion that Stabilises the Ligand-Free Receptor

Gebhard F X Schertler, Christopher Tate

PLoS ONE, 2014

View PDFchevron_right

Investigation of key interactions between the second extracellular loop of dopamine D2 receptor and several hydroxy-N-{[2-(4-phenyl-piperaziny-1-yl)ethyl]phenyl}-nicotinamides

Đurđica Ignjatović

Journal of the Serbian Chemical Society, 2014

View PDFchevron_right

Functional Role of the “Ionic Lock”—An Interhelical Hydrogen-Bond Network in Family A Heptahelical Receptors

Friedrich Siebert

Journal of Molecular Biology, 2008

View PDFchevron_right

Interaction of permanently charged analogs of dopamine with the D-2 dopaminergic receptor

Tahira Farooqui

Biochemical Pharmacology, 1987

View PDFchevron_right

Structural Determinants of Pharmacological Specificity Between D1 and D2 Dopamine Receptors

Curtiss Durand

Molecular Pharmacology, 2005

View PDFchevron_right

The influence of dispersive interactions on the binding affinities of ligands with an arylpiperazine moiety to the dopamine D2 receptor

Goran Roglic

Journal of the Serbian Chemical Society, 2009

View PDFchevron_right

Silencing of the Constitutive Activity of the Dopamine D1B Receptor. RECIPROCAL MUTATIONS BETWEEN D1 RECEPTOR SUBTYPES DELINEATE RESIDUES UNDERLYING ACTIVATION PROPERTIES

Mario Tiberi

Journal of Biological Chemistry, 1996

View PDFchevron_right