International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and classification of adenosine receptors—an update

BB Fredholm, AP IJzerman, KA Jacobson… - Pharmacological …, 2011 - ASPET
In the 10 years since our previous International Union of Basic and Clinical Pharmacology
report on the nomenclature and classification of adenosine receptors, no developments …

International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors

BB Fredholm, AP IJzerman, KA Jacobson… - Pharmacological …, 2001 - ASPET
Four adenosine receptors have been cloned and characterized from several mammalian
species. The receptors are named adenosine A1, A2A, A2B, and A3. The A2A and A2B …

The 2.6 Angstrom Crystal Structure of a Human A2A Adenosine Receptor Bound to an Antagonist

VP Jaakola, MT Griffith, MA Hanson, V Cherezov… - Science, 2008 - science.org
The adenosine class of heterotrimeric guanine nucleotide–binding protein (G protein)–
coupled receptors (GPCRs) mediates the important role of extracellular adenosine in many …

Serotonin receptors

DE Nichols, CD Nichols - Chemical reviews, 2008 - ACS Publications
Serotonin, 5-hydroxytryptamine (5-HT), is one of the class of monoamine neurontransmitters,
all of which have a chemical template comprised of a basic amino group separated from an …

[HTML][HTML] Mechanistic insights into allosteric regulation of the A2A adenosine G protein-coupled receptor by physiological cations

L Ye, C Neale, A Sljoka, B Lyda, D Pichugin… - Nature …, 2018 - nature.com
Cations play key roles in regulating G-protein-coupled receptors (GPCRs), although their
mechanisms are poorly understood. Here, 19F NMR is used to delineate the effects of …

Molecular mechanisms of ligand binding, signaling, and regulation within the superfamily of G-protein-coupled receptors: molecular modeling and mutagenesis …

K Kristiansen - Pharmacology & therapeutics, 2004 - Elsevier
The superfamily of G-protein-coupled receptors (GPCRs) could be subclassified into 7
families (A, B, large N-terminal family B-7 transmembrane helix, C, Frizzled/Smoothened …

The binding site of aminergic G protein–coupled receptors: the transmembrane segments and second extracellular loop

L Shi, JA Javitch - Annual review of pharmacology and …, 2002 - annualreviews.org
In the current chapter, we review approaches to the identification of the residues forming the
binding sites for agonists, antagonists, and allosteric modulators in the family of aminergic G …

A candidate olfactory receptor subtype highly conserved across different insect orders

J Krieger, O Klink, C Mohl, K Raming… - Journal of Comparative …, 2003 - Springer
Candidate olfactory receptors of the moth Heliothis virescens were found to be extremely
diverse from receptors of the fruitfly Drosophila melanogaster and the mosquito Anopheles …

Community-wide assessment of GPCR structure modelling and ligand docking: GPCR Dock 2008

M Michino, E Abola… - Nature Reviews Drug …, 2009 - nature.com
Recent breakthroughs in the determination of the crystal structures of G protein-coupled
receptors (GPCRs) have provided new opportunities for structure-based drug design …

Structure-based drug discovery using GPCR homology modeling: successful virtual screening for antagonists of the alpha1A adrenergic receptor

A Evers, T Klabunde - Journal of medicinal chemistry, 2005 - ACS Publications
In this paper, we describe homology modeling of the alpha1A receptor based on the X-ray
structure of bovine rhodopsin. The protein model has been generated by applying ligand …