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6l2d

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'''Unreleased structure'''
 
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The entry 6l2d is ON HOLD
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==Crystal structure of a cupin protein (tm1459) in copper (Cu) substituted form==
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<StructureSection load='6l2d' size='340' side='right'caption='[[6l2d]], [[Resolution|resolution]] 1.20&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6l2d]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Thermotoga_maritima_MSB8 Thermotoga maritima MSB8]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6L2D OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6L2D FirstGlance]. <br>
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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]] 1.198&#8491;</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=CSD:3-SULFINOALANINE'>CSD</scene>, <scene name='pdbligand=CU:COPPER+(II)+ION'>CU</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=6l2d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6l2d OCA], [https://pdbe.org/6l2d PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6l2d RCSB], [https://www.ebi.ac.uk/pdbsum/6l2d PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6l2d ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/Q9X1H0_THEMA Q9X1H0_THEMA]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Cupin superfamily proteins (TM1459) work as a macromolecular ligand framework with a double-stranded beta-barrel structure ligating to a Cu ion through histidine side chains. Variegating the first coordination sphere of TM1459 revealed that H52A and H54A/H58A mutants effectively catalyzed the diastereo- and enantioselective Michael addition reaction of nitroalkanes to an alpha,beta-unsaturated ketone. Moreover, calculated substrate docking signified C106N and F104W single-point mutations, which inverted the diastereoselectivity of H52A and further improved the stereoselectivity of H54A/H58A, respectively.
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Authors: Fujieda, N., Ichihashi, H., Nishikawa, Y., Kurisu, G., Itoh, S.
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Cupin Variants as a Macromolecular Ligand Library for Stereoselective Michael Addition of Nitroalkanes.,Fujieda N, Ichihashi H, Yuasa M, Nishikawa Y, Kurisu G, Itoh S Angew Chem Int Ed Engl. 2020 Feb 19. doi: 10.1002/anie.202000129. PMID:32073197<ref>PMID:32073197</ref>
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Description: Crystal structure of a cupin protein (tm1459) in copper (Cu) substituted form
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Kurisu, G]]
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<div class="pdbe-citations 6l2d" style="background-color:#fffaf0;"></div>
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[[Category: Itoh, S]]
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== References ==
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[[Category: Ichihashi, H]]
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<references/>
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[[Category: Nishikawa, Y]]
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__TOC__
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[[Category: Fujieda, N]]
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Thermotoga maritima MSB8]]
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[[Category: Fujieda N]]
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[[Category: Ichihashi H]]
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[[Category: Itoh S]]
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[[Category: Kurisu G]]
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[[Category: Nishikawa Y]]

Current revision

Crystal structure of a cupin protein (tm1459) in copper (Cu) substituted form

PDB ID 6l2d

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