Structure and Function Relationship of Murine Insulin-like Peptide 5 (INSL5): Free C-Terminus Is Essential for RXFP4 Receptor Binding and Activation-Reference-Cited by-同舟云学术

Structure and Function Relationship of Murine Insulin-like Peptide 5 (INSL5): Free C-Terminus Is Essential for RXFP4 Receptor Binding and Activation

Published:2011-09-08 Issue:39 Volume:50 Page:8352-8361
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Belgi Alessia¹,Hossain Mohammed A.¹,Shabanpoor Fazel¹,Chan Linda¹,Zhang Suode¹,Bathgate Ross A. D.¹,Tregear Geoffrey W.¹,Wade John D.¹

Affiliation:

1. Florey Neuroscience Institutes, ‡Department of Biochemistry and Molecular Biology, and §School of Chemistry, The University of Melbourne, Victoria 3010, Australia

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi201093m

Reference19 articles.

1. Chapter 1 The Human Insulin Superfamily of Polypeptide Hormones

2. Identification of INSL5, a New Member of the Insulin Superfamily

3. INSL5 Is a High Affinity Specific Agonist for GPCR142 (GPR100)

4. Structure of human insulin-like peptide 5 and characterization of conserved hydrogen bonds and electrostatic interactions within the relaxin framework

5. Takeda Cambridge Ltd. PatentCooperation Treaty (PCT), International Application Number PCT/GB2008/003023,International Filing Date: 5 September (2008.

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