View source for 2lur


==NMR solution structure of Kb1[ghrw;23-28]==
<StructureSection load='2lur' size='340' side='right'caption='[[2lur]]' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[2lur]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LUR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LUR FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR, 20 models</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2lur FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lur OCA], [https://pdbe.org/2lur PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lur RCSB], [https://www.ebi.ac.uk/pdbsum/2lur PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lur ProSAT]</span></td></tr>
</table>
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== Publication Abstract from PubMed ==
Obesity is an increasingly important global health problem that lacks current treatment options. The melanocortin receptor 4 (MC4R) is a target for obesity therapies because its activation triggers appetite suppression and increases energy expenditure. Cyclotides have been suggested as scaffolds for the insertion and stabilization of pharmaceutically active peptides. In this study, we explored the development of appetite-reducing peptides by synthesizing MC4R agonists based on the insertion of the His-Phe-Arg-Trp sequence into the cyclotide kalata B1. The ability of the analogues to fold similarly to kalata B1 but display MC4R activity were investigated. Four peptides were synthesized using t-butoxycarbonyl peptide chemistry with a C-terminal thioester to facilitate backbone cyclization. The structures of the peptides were found to be similar to kalata B1, evaluated by Halpha NMR chemical shifts. KB1(GHFRWG;23-28) had a K(i) of 29 nm at the MC4R and was 107 or 314 times more selective over this receptor than MC1R or MC5R, respectively, and had no detectable binding to MC3R. The peptide had higher affinity for the MC4R than the endogenous agonist, alpha-melanocyte stimulation hormone, but it was less potent at the MC4R, with an EC(50) of 580 nm for activation of the MC4R. In conclusion, we synthesized melanocortin analogues of kalata B1 that preserve the structural scaffold and display receptor binding and functional activity. KB1(GHFRWG;23-28) is potent and selective for the MC4R. This compound validates the use of cyclotides as scaffolds and has the potential to be a new lead for the treatment of obesity.

Design, synthesis, structural and functional characterization of novel melanocortin agonists based on the cyclotide kalata b1.,Eliasen R, Daly NL, Wulff BS, Andresen TL, Conde-Frieboes KW, Craik DJ J Biol Chem. 2012 Nov 23;287(48):40493-501. doi: 10.1074/jbc.M112.395442. Epub, 2012 Sep 25. PMID:23012369<ref>PMID:23012369</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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== References ==
<references/>
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</StructureSection>
[[Category: Large Structures]]
[[Category: Craik DJ]]
[[Category: Daly NL]]
[[Category: Eliasen R]]