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Science, ISSN 0036-8075, 2/2012, Volume 335, Issue 6070, pp. 851 - 855
Journal Article
Journal Article
Science, ISSN 0036-8075, 11/2008, Volume 322, Issue 5905, pp. 1211 - 1217
Journal Article
Science, ISSN 0036-8075, 11/2007, Volume 318, Issue 5854, pp. 1258 - 1265
Heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptors constitute the largest family of eukaryotic signal transduction proteins that... 
Proteins | Molecules | Receptors | Crystals | Data collection | Ligands | Lipids | Cell membranes | Research Articles | Cholesterols | Crystal structure
Journal Article
Science, ISSN 0036-8075, 11/2007, Volume 318, Issue 5854, pp. 1266 - 1273
The β₂-adrenergic receptor (β₂AR) is a well-studied prototype for heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptors (GPCRs) that... 
Proteins | Molecules | Receptors | Drug interactions | Crystallization | Crystals | Agonists | Ligands | Amino acids | Research Articles | Crystal structure
Journal Article
Journal Article
Nature Communications, ISSN 2041-1723, 05/2017, Volume 8, Issue 1, pp. 15383 - 15383
Journal Article
Nature, ISSN 0028-0836, 06/2017, Volume 546, Issue 7657, pp. 259 - 264
The human glucagon receptor, GCGR, belongs to the class B G-protein-coupled receptor family and plays a key role in glucose homeostasis and the pathophysiology... 
REFINEMENT | EXTRACELLULAR DOMAINS | LIPIDIC CUBIC PHASE | CORTICOTROPIN-RELEASING-FACTOR | MULTIDISCIPLINARY SCIENCES | DRUG DISCOVERY | VALIDATION | BINDING-SITE | SERIAL FEMTOSECOND CRYSTALLOGRAPHY | LIGAND | SOFTWARE | Receptors, Glucagon - agonists | Cross-Linking Reagents - chemistry | Allosteric Site - drug effects | Humans | Benzamides - metabolism | Models, Molecular | Receptors, Glucagon - metabolism | Crystallography, X-Ray | Receptors, Glucagon - classification | Molecular Dynamics Simulation | Deuterium Exchange Measurement | Disulfides - chemistry | Phenylurea Compounds - chemistry | Receptors, Glucagon - chemistry | Protein Domains | Ligands | Benzamides - pharmacology | Cell Membrane - metabolism | Phenylurea Compounds - metabolism | Phenylurea Compounds - pharmacology | Protein Stability | Benzamides - chemistry | Protein structure prediction | G proteins | Glucagon | Structure | Health aspects | Methods | Deuterium | Dynamic structural analysis | Exchanging | G protein-coupled receptors | Molecular structure | Hydrogen | Hydrogen-deuterium exchange | Diabetes mellitus | Homeostasis | Molecular dynamics | Crosslinking | Forming | Activation | Glucose | Guanine nucleotide-binding protein | Coupling (molecular) | Proteins | Signaling | Receptors | Receptor mechanisms | Diabetes | Protein structure | Crystal structure | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 06/2017, Volume 546, Issue 7657, pp. 312 - 315
The glucagon-like peptide-1 receptor (GLP-1R) and the glucagon receptor (GCGR) are members of the secretin-like class B family of G-protein-coupled receptors... 
MOLECULAR SIMULATION | ANTAGONIST | GLUCAGON-LIKE PEPTIDE-1 | DETERMINANTS | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | PROTEIN-COUPLED RECEPTORS | FORCE-FIELD | LIGAND | BINDING | AGONIST | Allosteric Regulation - drug effects | Amino Acid Sequence | Allosteric Site - drug effects | Humans | Benzamides - metabolism | Glucagon-Like Peptide-1 Receptor - chemistry | Models, Molecular | Crystallography, X-Ray | Aminopyridines - metabolism | Aminopyridines - chemistry | Glucagon-Like Peptide-1 Receptor - metabolism | Phenylurea Compounds - chemistry | Aminopyridines - pharmacology | Protein Domains | Benzamides - pharmacology | Phenylurea Compounds - metabolism | Phenylurea Compounds - pharmacology | Glucagon-Like Peptide-1 Receptor - agonists | Benzamides - chemistry | Type 2 diabetes | Physiological aspects | Glucagon | Health aspects | Protein-protein interactions | Membrane proteins | G protein-coupled receptors | Molecular structure | Peptides | Secretin | Activation | Helices | Glucose | Guanine nucleotide-binding protein | Modulators | Coupling (molecular) | Receptors | Allosteric properties | Modulation | Modelling | Physiology | Glucagon-like peptide 1 | Activation analysis | Crystal structure | Movement | Secretion | Diabetes mellitus | Insulin | Molecular modelling | Mutagenesis | Diabetes | Intracellular | Binding sites | Index Medicus
Journal Article