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Volumn 1160, Issue , 2009, Pages 74-77

Modeling the primary hormone-binding site of RXFP1 and RXFP2

Author keywords

GPCR; LDL A; LGR7; LGR8; Molecular modeling; RXFP1; RXFP2

Indexed keywords

HORMONE RECEPTOR; PROTEIN RXFP1; PROTEIN RXFP2; RELAXIN; RELAXIN LIKE FACTOR; UNCLASSIFIED DRUG;

EID: 64549145456     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2009.03950.x     Document Type: Conference Paper
Times cited : (16)

References (10)
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  • 2
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  • 3
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    • Defining the LGR8 residues involved in binding insulin-like peptide 3
    • Scott, D.J., T.N. Wilkinson, S. Zhang, et al. 2007. Defining the LGR8 residues involved in binding insulin-like peptide 3. Mol. Endocrinol. 21: 1699-1712.
    • (2007) Mol. Endocrinol , vol.21 , pp. 1699-1712
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  • 4
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    • The receptor-binding site of human relaxin II. A dual prong-binding mechanism
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    • H3 relaxin is a specific ligand for LGR7 and activates the receptor by interacting with both the ectodomain and the exoloop 2
    • Sudo, S., J. Kumagai, S. Nishi, et al. 2003. H3 relaxin is a specific ligand for LGR7 and activates the receptor by interacting with both the ectodomain and the exoloop 2. J. Biol. Chem. 278: 7855-7862.
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    • Characterization of the rat INSL3 receptor
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    • Identification of binding sites with differing affinity and potency for relaxin analogues on LGR7 and LGR8 receptors
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    • Fan, Q.R. & W.A. Hendrickson. 2005. Structure of human follicle-stimulating hormone in complex with its receptor. Nature 433: 269-277.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.