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3imo

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<StructureSection load='3imo' size='340' side='right'caption='[[3imo]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
<StructureSection load='3imo' size='340' side='right'caption='[[3imo]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[3imo]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Vibrio_cholerae_o139 Vibrio cholerae o139]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3IMO OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3IMO FirstGlance]. <br>
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<table><tr><td colspan='2'>[[3imo]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Vibrio_cholerae_O139 Vibrio cholerae O139]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3IMO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3IMO FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
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<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=3imo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3imo OCA], [http://pdbe.org/3imo PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=3imo RCSB], [http://www.ebi.ac.uk/pdbsum/3imo PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=3imo ProSAT]</span></td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3imo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3imo OCA], [https://pdbe.org/3imo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3imo RCSB], [https://www.ebi.ac.uk/pdbsum/3imo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3imo ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
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== Function ==
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== Publication Abstract from PubMed ==
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[https://www.uniprot.org/uniprot/C7U313_VIBCL C7U313_VIBCL]
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Mobile gene cassettes captured within integron arrays encompass a vast and diverse pool of genetic novelty. In most cases, functional annotation of gene cassettes directly recovered by cassette-PCR is obscured by their characteristically high sequence novelty. This inhibits identification of those specific functions or biological features that might constitute preferential factors for lateral gene transfer via the integron system. A structural genomics approach incorporating x-ray crystallography has been utilised on a selection of cassettes to investigate evolutionary relationships hidden at the sequence level. Gene cassettes were accessed from marine sediments (pristine and contaminated sites), as well as a range of Vibrio spp. We present six crystal structures, a remarkably high proportion of our survey of soluble proteins, which were found to possess novel folds. These entirely new structures are diverse, encompassing all-alpha, alpha+beta and alpha/beta fold classes, and many contain clear binding pocket features for small molecule substrates. The new structures emphasise the large repertoire of protein families encoded within the integron cassette metagenome and which remain to be characterised. Oligomeric association is a notable recurring property common to these new integron-derived proteins. In some cases, the protein-protein contact sites utilised in homomeric assembly could instead form suitable contact points for heterogeneous regulator/activator proteins or domains. Such functional features are ideal for a flexible molecular componentry needed to ensure responsive and adaptive bacterial functions.
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Integron gene cassettes: a repository of novel protein folds with distinct interaction sites.,Sureshan V, Deshpande CN, Boucher Y, Koenig JE, Stokes HW, Harrop SJ, Curmi PM, Mabbutt BC PLoS One. 2013;8(1):e52934. doi: 10.1371/journal.pone.0052934. Epub 2013 Jan 18. PMID:23349695<ref>PMID:23349695</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 3imo" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Vibrio cholerae o139]]
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[[Category: Vibrio cholerae O139]]
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[[Category: Boucher, Y]]
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[[Category: Boucher Y]]
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[[Category: Curmi, P M.G]]
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[[Category: Curmi PMG]]
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[[Category: Deshpande, C N]]
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[[Category: Deshpande CN]]
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[[Category: Harrop, S J]]
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[[Category: Harrop SJ]]
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[[Category: Mabbutt, B C]]
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[[Category: Mabbutt BC]]
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[[Category: Stokes, H W]]
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[[Category: Stokes HW]]
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[[Category: Sureshan, V]]
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[[Category: Sureshan V]]
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[[Category: Argentinean o139 strain]]
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[[Category: Integron protein]]
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[[Category: Novel]]
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[[Category: Unknown function]]
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[[Category: Vibrio cholerae]]
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Current revision

Structure from the mobile metagenome of Vibrio cholerae. Integron cassette protein VCH_CASS14

PDB ID 3imo

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