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| | <StructureSection load='4aky' size='340' side='right'caption='[[4aky]], [[Resolution|resolution]] 2.60Å' scene=''> | | <StructureSection load='4aky' size='340' side='right'caption='[[4aky]], [[Resolution|resolution]] 2.60Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[4aky]] is a 5 chain structure with sequence from [http://en.wikipedia.org/wiki/Atcc_23444 Atcc 23444]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4AKY OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4AKY FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4aky]] is a 5 chain structure with sequence from [https://en.wikipedia.org/wiki/Brucella_suis Brucella suis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4AKY OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4AKY FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=4LL:2-(BUTYLAMINO)QUINOLIN-8-OL'>4LL</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.6Å</td></tr> |
| - | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2bhm|2bhm]], [[4akz|4akz]]</td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=4LL:2-(BUTYLAMINO)QUINOLIN-8-OL'>4LL</scene></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4aky FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4aky OCA], [http://pdbe.org/4aky PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4aky RCSB], [http://www.ebi.ac.uk/pdbsum/4aky PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4aky ProSAT]</span></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=4aky FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4aky OCA], [https://pdbe.org/4aky PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4aky RCSB], [https://www.ebi.ac.uk/pdbsum/4aky PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4aky ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/VIRB8_BRUSU VIRB8_BRUSU]] The VirB system could be required for the establishment of the replication niche in the host. | + | [https://www.uniprot.org/uniprot/VIRB8_BRUSU VIRB8_BRUSU] The VirB system could be required for the establishment of the replication niche in the host. |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Atcc 23444]] | + | [[Category: Brucella suis]] |
| - | [[Category: Baron, C]] | + | [[Category: Large Structures]] |
| - | [[Category: Coincon, M]] | + | [[Category: Baron C]] |
| - | [[Category: Smith, M A]] | + | [[Category: Coincon M]] |
| - | [[Category: Sygusch, J]] | + | [[Category: Smith MA]] |
| - | [[Category: Bacterial type iv secretion]] | + | [[Category: Sygusch J]] |
| - | [[Category: Transport protein]]
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| Structural highlights
Function
VIRB8_BRUSU The VirB system could be required for the establishment of the replication niche in the host.
Publication Abstract from PubMed
Secretion systems translocate virulence factors of many bacterial pathogens, enabling their survival inside the host organism. Consequently, inhibition strongly attenuates pathogenicity and can be considered a target for novel antimicrobial drugs. The type IV secretion system (T4SS) of the intracellular pathogen Brucella is a prerequisite for its virulence, and in this work we targeted the interactions of the essential assembly factor protein, VirB8, using small-molecule inhibitors. High-throughput screening identified several potent and specific inhibitors, and the target-binding site of these inhibitors was identified by X-ray crystallography, in silico docking, and analysis of the derivates of the inhibitor B8I-2. VirB8 interaction inhibitors bind to a surface groove opposite to the dimerization interface, and by varying the binding-site residues, we were able to determine which residues are required for inhibitor activity. E115 and K182 were found to be especially important, and changes at R114, Y229, and L151 also reduced inhibitor efficiency.
Identification of the Binding Site of Brucella VirB8 Interaction Inhibitors.,Smith MA, Coincon M, Paschos A, Jolicoeur B, Lavallee P, Sygusch J, Baron C Chem Biol. 2012 Aug 24;19(8):1041-8. PMID:22921071[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Smith MA, Coincon M, Paschos A, Jolicoeur B, Lavallee P, Sygusch J, Baron C. Identification of the Binding Site of Brucella VirB8 Interaction Inhibitors. Chem Biol. 2012 Aug 24;19(8):1041-8. PMID:22921071 doi:http://dx.doi.org/10.1016/j.chembiol.2012.07.007
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