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4kyk

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(New page: '''Unreleased structure''' The entry 4kyk is ON HOLD Authors: Zhai, J., Yuan, M., Zhang, L., Chen, Y., Zhang, H., Chen, S., Zhao, Y. Description: Crystal structure of mouse glyoxalase ...)
Current revision (19:23, 29 May 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 4kyk is ON HOLD
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==Crystal structure of mouse glyoxalase I complexed with indomethacin==
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<StructureSection load='4kyk' size='340' side='right'caption='[[4kyk]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4kyk]] is a 2 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=4KYK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4KYK 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]] 2&#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=IMN:INDOMETHACIN'>IMN</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</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=4kyk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4kyk OCA], [https://pdbe.org/4kyk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4kyk RCSB], [https://www.ebi.ac.uk/pdbsum/4kyk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4kyk ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/LGUL_MOUSE LGUL_MOUSE] Catalyzes the conversion of hemimercaptal, formed from methylglyoxal and glutathione, to S-lactoylglutathione. Involved in the regulation of TNF-induced transcriptional activity of NF-kappa-B (By similarity).
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Old drugs new tricks: Zopolrestat, an aldose reductase inhibitor developed by Pfizer for the treatment of diabetic complications, is a potent competition inhibitor of human glyoxalase I (GLOI) in vitro. Crystal structures of GLOI in complex with zopolrestat and indomethacin, a nonsteroidal anti-inflammatory drug and moderate inhibitor of GLOI, provide a structural basis for the development of novel GLOI inhibitors with excellent pharmacokinetics profiles.
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Authors: Zhai, J., Yuan, M., Zhang, L., Chen, Y., Zhang, H., Chen, S., Zhao, Y.
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Zopolrestat as a Human Glyoxalase I Inhibitor and Its Structural Basis.,Zhai J, Zhang H, Zhang L, Zhao Y, Chen S, Chen Y, Peng X, Li Q, Yuan M, Hu X ChemMedChem. 2013 Jul 15. doi: 10.1002/cmdc.201300243. PMID:23857942<ref>PMID:23857942</ref>
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Description: Crystal structure of mouse glyoxalase I complexed with indomethacin
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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 4kyk" style="background-color:#fffaf0;"></div>
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==See Also==
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*[[Glyoxalase 3D structures|Glyoxalase 3D structures]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Mus musculus]]
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[[Category: Chen S]]
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[[Category: Chen Y]]
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[[Category: Yuan M]]
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[[Category: Zhai J]]
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[[Category: Zhang H]]
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[[Category: Zhang L]]
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[[Category: Zhao Y]]

Current revision

Crystal structure of mouse glyoxalase I complexed with indomethacin

PDB ID 4kyk

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