View source for 2mbk


==The Clip-segment of the von Willebrand domain 1 of the BMP modulator protein Crossveinless 2 is preformed==
<StructureSection load='2mbk' size='340' side='right'caption='[[2mbk]]' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[2mbk]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Danio_rerio Danio rerio]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MBK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2MBK FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR, 10 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=2mbk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2mbk OCA], [https://pdbe.org/2mbk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2mbk RCSB], [https://www.ebi.ac.uk/pdbsum/2mbk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2mbk ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/Q5D734_DANRE Q5D734_DANRE] 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Bone Morphogenetic Proteins (BMPs) are secreted protein hormones that act as morphogens and exert essential roles during embryonic development of tissues and organs. Signaling by BMPs occurs via hetero-oligomerization of two types of serine/threonine kinase transmembrane receptors. Due to the small number of available receptors for a large number of BMP ligands ligand-receptor promiscuity presents an evident problem requiring additional regulatory mechanisms for ligand-specific signaling. Such additional regulation is achieved through a plethora of extracellular antagonists, among them members of the Chordin superfamily, that modulate BMP signaling activity by binding. The key-element in Chordin-related antagonists for interacting with BMPs is the von Willebrand type C (VWC) module, which is a small domain of about 50 to 60 residues occurring in many different proteins. Although a structure of the VWC domain of the Chordin-member Crossveinless 2 (CV2) bound to BMP-2 has been determined by X-ray crystallography, the molecular mechanism by which the VWC domain binds BMPs has remained unclear. Here we present the NMR structure of the Danio rerio CV2 VWC1 domain in its unbound state showing that the key features for high affinity binding to BMP-2 is a pre-oriented peptide loop.

The Clip-Segment of the von Willebrand Domain 1 of the BMP Modulator Protein Crossveinless 2 Is Preformed.,Fiebig JE, Weidauer SE, Qiu LY, Bauer M, Schmieder P, Beerbaum M, Zhang JL, Oschkinat H, Sebald W, Mueller TD Molecules. 2013 Sep 25;18(10):11658-82. doi: 10.3390/molecules181011658. PMID:24071977<ref>PMID:24071977</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 2mbk" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Danio rerio]]
[[Category: Large Structures]]
[[Category: Bauer M]]
[[Category: Beerbaum M]]
[[Category: Fiebig JE]]
[[Category: Mueller TD]]
[[Category: Oschkinat H]]
[[Category: Qiu L]]
[[Category: Schmieder P]]
[[Category: Sebald W]]
[[Category: Weidauer SE]]
[[Category: Zhang J]]