View source for 5wip


==TraE protein in complex with 2-(2-furyl)isonicotinic acid==
<StructureSection load='5wip' size='340' side='right'caption='[[5wip]], [[Resolution|resolution]] 2.62&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[5wip]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5WIP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5WIP 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]] 2.62&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=XXO:2-(furan-2-yl)pyridine-4-carboxylic+acid'>XXO</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=5wip FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5wip OCA], [https://pdbe.org/5wip PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5wip RCSB], [https://www.ebi.ac.uk/pdbsum/5wip PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5wip ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/Q17U16_ECOLX Q17U16_ECOLX] 
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The increasing frequency of antimicrobial resistance is a problem of global importance. Novel strategies are urgently needed to understand and inhibit antimicrobial resistance gene transmission that is mechanistically related to bacterial virulence functions. The conjugative transfer of plasmids by type IV secretion systems is a major contributor to antimicrobial resistance gene transfer. Here, we present a structure-based strategy to identify inhibitors of type IV secretion system-mediated bacterial conjugation. Using differential scanning fluorimetry we screened a fragment library and identified molecules that bind the essential TraE protein of the plasmid pKM101 conjugation machinery. Co-crystallization revealed that fragments bind two alternative sites of the protein and one of them is a novel inhibitor binding site. Based on the structural information on fragment binding we designed novel small molecules that have improved binding affinity. These molecules inhibit the dimerization of TraE, bind to both inhibitor binding sites on TraE and inhibit the conjugative transfer of plasmid pKM101. The strategy presented here is generally applicable for the structure-based design of inhibitors of antimicrobial resistance gene transfer and of bacterial virulence.

Fragment-based screening identifies novel targets for inhibitors of conjugative transfer of antimicrobial resistance by plasmid pKM101.,Casu B, Arya T, Bessette B, Baron C Sci Rep. 2017 Nov 2;7(1):14907. doi: 10.1038/s41598-017-14953-1. PMID:29097752<ref>PMID:29097752</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 5wip" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Escherichia coli]]
[[Category: Large Structures]]
[[Category: Arya T]]
[[Category: Baron C]]
[[Category: Bessette B]]
[[Category: Casu B]]