Stalk-dependent and stalk-independent signaling by the adhesion G protein-coupled receptors GPR56 (ADGRG1) and BAI1 (ADGRB1)

Journal of Biological Chemistry

Volumn 291, Issue 7, 2016, Pages 3385-3394

  Kishore, Ayush ^a   Purcell, Ryan H ^a   Nassiri Toosi, Zahra ^a   Hall, Randy A ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION ANALYSIS; ADHESION; ASSAYS; BIOLOGICAL MEMBRANES; CHEMICAL ACTIVATION; PROTEINS;

DATA SUPPORT; G PROTEIN COUPLED RECEPTORS; MULTIPLE ASSAYS; N-TERMINALS; SEVEN-TRANSMEMBRANE PROTEINS; SIGNALING ACTIVITY; TRANS-MEMBRANE DOMAINS; WILD TYPES;

SIGNALING;

ADHESION G PROTEIN COUPLED RECEPTOR GPR56; ADHESION G PROTEIN COUPLED RECEPTOR GPRB1; BETA ARRESTIN; RECEPTOR; UNCLASSIFIED DRUG; ANGIOGENIC PROTEIN; BAI1 PROTEIN, HUMAN; G PROTEIN COUPLED RECEPTOR; GPR56 PROTEIN, HUMAN; HYBRID PROTEIN; LIGAND; PEPTIDE FRAGMENT; RECOMBINANT PROTEIN; RETINA S ANTIGEN; TGFA PROTEIN, HUMAN; TRANSCRIPTION FACTOR NFAT; TRANSFORMING GROWTH FACTOR ALPHA;

AMINO TERMINAL SEQUENCE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; INTRACELLULAR SIGNALING; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; UBIQUITINATION; AGONISTS; ALLOSTERISM; AMINO ACID SUBSTITUTION; CHEMISTRY; CONSERVED SEQUENCE; GENETICS; HEK293 CELL LINE; HUMAN; METABOLISM; MOLECULAR MODEL; POINT MUTATION; PROTEIN CONFORMATION; PROTEIN DEGRADATION; REPORTER GENE; SIGNAL TRANSDUCTION;

ALLOSTERIC REGULATION; AMINO ACID SUBSTITUTION; ANGIOGENIC PROTEINS; ARRESTINS; BETA-ARRESTINS; CONSERVED SEQUENCE; GENES, REPORTER; HEK293 CELLS; HUMANS; LIGANDS; MODELS, MOLECULAR; NFATC TRANSCRIPTION FACTORS; PEPTIDE FRAGMENTS; POINT MUTATION; PROTEIN CONFORMATION; PROTEIN INTERACTION DOMAINS AND MOTIFS; PROTEOLYSIS; RECEPTORS, G-PROTEIN-COUPLED; RECOMBINANT FUSION PROTEINS; RECOMBINANT PROTEINS; SIGNAL TRANSDUCTION; TRANSFORMING GROWTH FACTOR ALPHA; UBIQUITINATION;

EID: 84964679035     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M115.689349     Document Type: Article

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