3v0v: Difference between revisions

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New page: '''Unreleased structure''' The entry 3v0v is ON HOLD Authors: Gomery, K., Evans, S.V. Description: Fab WN1 222-5 unliganded
 
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'''Unreleased structure'''


The entry 3v0v is ON HOLD
==Fab WN1 222-5 unliganded==
<StructureSection load='3v0v' size='340' side='right'caption='[[3v0v]], [[Resolution|resolution]] 2.13&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[3v0v]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3V0V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3V0V 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]] 2.13&#8491;</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=3v0v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3v0v OCA], [https://pdbe.org/3v0v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3v0v RCSB], [https://www.ebi.ac.uk/pdbsum/3v0v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3v0v ProSAT]</span></td></tr>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Escherichia coli infections, a leading cause of septic shock, remain a major threat to human health because of the fatal action to endotoxin (LPS). Therapeutic attempts to neutralize endotoxin currently focus on inhibiting the interaction of the toxic component lipid A with myeloid differentiating factor 2, which forms a trimeric complex together with Toll-like receptor 4 to induce immune cell activation. The 1.73-A resolution structure of the unique endotoxin-neutralizing protective antibody WN1 222-5 in complex with the core region shows that it recognizes LPS of all E. coli serovars in a manner similar to Toll-like receptor 4, revealing that protection can be achieved by targeting the inner core of LPS and that recognition of lipid A is not required. Such interference with Toll-like receptor complex formation opens new paths for antibody sepsis therapy independent of lipid A antagonists.


Authors: Gomery, K., Evans, S.V.
Antibody WN1 222-5 mimics Toll-like receptor 4 binding in the recognition of LPS.,Gomery K, Muller-Loennies S, Brooks CL, Brade L, Kosma P, Di Padova F, Brade H, Evans SV Proc Natl Acad Sci U S A. 2012 Dec 18;109(51):20877-82. doi:, 10.1073/pnas.1209253109. Epub 2012 Nov 26. PMID:23184990<ref>PMID:23184990</ref>


Description: Fab WN1 222-5 unliganded
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 3v0v" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Mus musculus]]
[[Category: Evans SV]]
[[Category: Gomery K]]

Latest revision as of 06:15, 17 October 2024

Fab WN1 222-5 unliganded

3v0v, resolution 2.13Å

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