7uuc

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'''Unreleased structure'''
 
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The entry 7uuc is ON HOLD
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==Structure of the SARS-CoV-2 main protease in complex with inhibitor MPI19==
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<StructureSection load='7uuc' size='340' side='right'caption='[[7uuc]], [[Resolution|resolution]] 1.60&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7uuc]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Severe_acute_respiratory_syndrome_coronavirus_2 Severe acute respiratory syndrome coronavirus 2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7UUC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7UUC 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]] 1.6&#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=81L:(phenylmethyl)+~{N}-[(2~{S})-1-[[(2~{S})-3-cyclopropyl-1-oxidanylidene-1-[[(2~{S})-1-oxidanyl-3-[(3~{S})-2-oxidanylidenepyrrolidin-3-yl]propan-2-yl]amino]propan-2-yl]amino]-3,3-dimethyl-1-oxidanylidene-butan-2-yl]carbamate'>81L</scene>, <scene name='pdbligand=CSO:S-HYDROXYCYSTEINE'>CSO</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=7uuc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7uuc OCA], [https://pdbe.org/7uuc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7uuc RCSB], [https://www.ebi.ac.uk/pdbsum/7uuc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7uuc ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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As the COVID-19 pathogen, SARS-CoV-2 relies on its main protease (M(Pro)) for pathogenesis and replication. During crystallographic analyses of M(Pro) crystals that were exposed to the air, a uniquely Y-shaped, S-O-N-O-S-bridged post-translational cross-link that connects three residues C22, C44, and K61 at their side chains was frequently observed. As a novel covalent modification, this cross-link serves potentially as a redox switch to regulate the catalytic activity of M(Pro), a demonstrated drug target of COVID-19. The formation of this linkage leads to a much more open active site that can potentially be targeted for the development of novel SARS-CoV-2 antivirals. The structural rearrangement of M(Pro) by this cross-link indicates that small molecules that lock M(Pro) in the cross-linked form can potentially be used with other active-site-targeting molecules such as paxlovid for synergistic effects in inhibiting SARS-CoV-2 viral replication.
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Authors: Yang, K.S., Liu, W.R.
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A Novel Y-Shaped, S-O-N-O-S-Bridged Cross-Link between Three Residues C22, C44, and K61 Is Frequently Observed in the SARS-CoV-2 Main Protease.,Yang KS, Blankenship LR, Kuo SA, Sheng YJ, Li P, Fierke CA, Russell DH, Yan X, Xu S, Liu WR ACS Chem Biol. 2023 Mar 17;18(3):449-455. doi: 10.1021/acschembio.2c00695. Epub , 2023 Jan 11. PMID:36629751<ref>PMID:36629751</ref>
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Description: Structure of the SARS-CoV-2 main protease in complex with inhibitor MPI19
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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: Yang, K.S]]
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<div class="pdbe-citations 7uuc" style="background-color:#fffaf0;"></div>
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[[Category: Liu, W.R]]
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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: Severe acute respiratory syndrome coronavirus 2]]
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[[Category: Liu WR]]
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[[Category: Yang KS]]

Current revision

Structure of the SARS-CoV-2 main protease in complex with inhibitor MPI19

PDB ID 7uuc

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