Addition of a carboxy-terminal green fluorescent protein does not alter the binding and signaling properties of relaxin family peptide receptor 3

Annals of the New York Academy of Sciences

Volumn 1160, Issue , 2009, Pages 105-107

  Van Der Westhuizen, Emma T ^a   Wade, John D ^b   Sexton, Patrick M ^a   Summers, Roger J ^a  

^a MONASH UNIVERSITY   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

GPCR135; Green fluorescent protein; Relaxin 3; RXFP3; SALPR

Indexed keywords

CHIMERIC PROTEIN; G PROTEIN COUPLED RECEPTOR; GREEN FLUORESCENT PROTEIN; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; PROTEIN RXFP3; RELAXIN; UNCLASSIFIED DRUG;

ANIMAL CELL; CONFERENCE PAPER; HUMAN; HUMAN CELL; NONHUMAN; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; RECEPTOR BINDING; RECEPTOR INTRINSIC ACTIVITY; SIGNAL TRANSDUCTION;

EID: 64549159372     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2008.03818.x     Document Type: Conference Paper

References (4)

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2. Liu, C., E. Eriste, S. Sutton, et al. 2003. Identification of relaxin-3/INSL7 as an endogenous ligand for the orphan G-protein-coupled receptor GPCR135. J. Biol. Chem. 278: 50754-50764.
3. Van Der Westhuizen, E.T., T.D. Werry, P.M. Sexton, et al. 2007. The relaxin family peptide receptor 3 (RXFP3) activates ERK1/2 through a PKC dependent mechanism. Mol. Pharmacol. 71: 1618-1629.
4. Liu, C., J. Chen, C. Kuei, et al. 2005. Relaxin-3/insulin-like peptide 5 chimeric peptide, a selective ligand for G protein-coupled receptor (GPCR) 135 and GPCR142 over leucine-rich repeat-containing G protein-coupled receptor 7. Mol. Pharmacol. 67: 231-240.