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Nature, ISSN 0028-0836, 05/2017, Volume 545, Issue 7652, pp. 112 - 115
Protease-activated receptors ( PARs) are a family of G-proteincoupled receptors ( GPCRs) that are irreversibly activated by proteolytic cleavage of the N... 
PHENIX | THROMBIN | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | Allosteric Regulation - drug effects | Benzyl Alcohols - chemistry | Allosteric Site - drug effects | Humans | Receptor, PAR-2 - metabolism | Imidazoles - chemistry | Models, Molecular | Crystallography, X-Ray | Antibodies, Blocking - pharmacology | Imidazoles - pharmacology | Benzimidazoles - chemistry | Receptor, PAR-2 - chemistry | Immunoglobulin Fab Fragments - pharmacology | Receptor, PAR-2 - antagonists & inhibitors | Signal Transduction - drug effects | Antibodies, Blocking - chemistry | Immunoglobulin Fab Fragments - chemistry | Benzyl Alcohols - pharmacology | Benzimidazoles - pharmacology | Ligands | Benzodioxoles - chemistry | Kinetics | Benzodioxoles - pharmacology | Physiological aspects | Cell receptors | Allosteric proteins | Cytochrome | Residues | G protein-coupled receptors | Peptides | Molecular structure | Hydrogen | Homology | Antagonists | Hydrophobicity | Hydrogen bonding | Optimization | Proteins | Lipophilic | Allosteric properties | Imidazole | Cleavage | Inhibition | Thromboembolism | Lysozyme | Hydrogen ion concentration | Deoxyribonucleic acid--DNA | Cultivation | Architecture | Fab | Crystals | Crystallization | Pharmacology | Inflammation | Glycosylation | Computer programs | Chemistry | Diffraction | Antagonist drugs | Lysine | Isoforms | Computer applications | Mutation | Internet | Receptor mechanisms | Binding sites | Glutamine | Cancer
Journal Article
Cell and Tissue Research, ISSN 0302-766X, 3/2015, Volume 359, Issue 3, pp. 817 - 827
Journal Article
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 311 - 16
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2011, Volume 6, Issue 11, p. e28018
Protease-activated receptor-2 (PAR2) is a G protein coupled receptor (GPCR) activated by proteolytic cleavage of its amino terminal domain by trypsin-like... 
VASOPRESSIN RECEPTOR | 4TH CYTOPLASMIC LOOP | PHOSPHORYLATION | HELIX 8 | COUPLED RECEPTOR | BIOLOGY | ERK1/2 ACTIVATION | MOLECULAR-CLONING | FLUORESCENT PROTEIN | BETA-ADRENERGIC RECEPTOR | ARRESTIN-DEPENDENT ENDOCYTOSIS | Cricetulus | Humans | Receptor, PAR-2 - metabolism | Secretory Pathway | Molecular Sequence Data | Arrestins - metabolism | Endocytosis | Proteolysis | Cell Membrane - metabolism | Cysteine - metabolism | CHO Cells | rab GTP-Binding Proteins - metabolism | Amino Acid Sequence | Cricetinae | Lipoylation | Signal Transduction | Mutation - genetics | Receptor, PAR-2 - chemistry | Protein Transport | Animals | Models, Biological | beta-Arrestins | Receptor, PAR-2 - agonists | Golgi Apparatus - metabolism | Palmitates - metabolism | Cysteine | Trypsin | Proteases | Prostate cancer | Cystine | Plasma | Flow cytometry | Phosphorylation | G protein-coupled receptors | Peptides | Palmitoylation | Serine | Confocal microscopy | Labelling | Arrestin | Confocal | Kinases | Palmitic acid | Cell surface | Recruitment | Degradation | Proteins | Calcium signalling | Signal transduction | Par-2 protein | Protease | Life cycle engineering | Post-translation | Localization | Medical research | Biotinylation | Desensitization | Inflammation | Tumor cell lines | Golgi apparatus | Cytometry | Microscopy | Cell lines | Ligands | Membrane trafficking | Prostate | Chemokines | Cancer | Life cycles
Journal Article
Journal of Computer-Aided Molecular Design, ISSN 0920-654X, 08/2016, Volume 30, Issue 8, pp. 625 - 637
Journal Article
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 03/2006, Volume 281, Issue 11, pp. 6910 - 6923
Journal Article