7b01
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 7b01 is ON HOLD until sometime in the future Authors: Description: Category: Unreleased Structures) |
|||
| (7 intermediate revisions not shown.) | |||
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | + | ==ADAMTS13-CUB12== | |
| + | <StructureSection load='7b01' size='340' side='right'caption='[[7b01]], [[Resolution|resolution]] 2.80Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7B01 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7B01 FirstGlance]. <br> | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.8Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GLC:ALPHA-D-GLUCOSE'>GLC</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></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=7b01 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7b01 OCA], [https://pdbe.org/7b01 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7b01 RCSB], [https://www.ebi.ac.uk/pdbsum/7b01 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7b01 ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | ADAMTS13 is a plasma metalloprotease that is essential for the regulation of von Willebrand factor (VWF) function, mediator of platelet recruitment to sites of blood vessel damage. ADAMTS13 function is dynamically regulated by structural changes induced by VWF binding that convert it from a latent to active conformation. ADAMTS13 global latency is manifest by the interaction of its C-terminal CUB1-2 domains with its central Spacer domain. We resolved the crystal structure of the ADAMTS13 CUB1-2 domains revealing a previously unreported configuration for the tandem CUB domains. Docking simulations between the CUB1-2 domains with the Spacer domain in combination with enzyme kinetic functional characterization of ADAMTS13 CUB domain mutants enabled the mapping of the CUB1-2 domain site that binds the Spacer domain. Together, these data reveal the molecular basis of the ADAMTS13 Spacer-CUB interaction and the control of ADAMTS13 global latency. | ||
| - | + | Crystal structure of ADAMTS13 CUB domains reveals their role in global latency.,Kim HJ, Xu Y, Petri A, Vanhoorelbeke K, Crawley JTB, Emsley J Sci Adv. 2021 Apr 16;7(16). pii: 7/16/eabg4403. doi: 10.1126/sciadv.abg4403., Print 2021 Apr. PMID:33863735<ref>PMID:33863735</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | [[Category: | + | </div> |
| + | <div class="pdbe-citations 7b01" style="background-color:#fffaf0;"></div> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Emsley J]] | ||
| + | [[Category: Kim HJ]] | ||
Current revision
ADAMTS13-CUB12
| |||||||||||
