5rfa: Difference between revisions

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<StructureSection load='5rfa' size='340' side='right'caption='[[5rfa]], [[Resolution|resolution]] 1.52&Aring;' scene=''>
<StructureSection load='5rfa' size='340' side='right'caption='[[5rfa]], [[Resolution|resolution]] 1.52&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[5rfa]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5RFA OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5RFA FirstGlance]. <br>
<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5RFA OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5RFA FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene>, <scene name='pdbligand=JGY:1-methyl-N-{[(2S)-oxolan-2-yl]methyl}-1H-pyrazole-3-carboxamide'>JGY</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]] 1.52&#8491;</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=5rfa FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5rfa OCA], [http://pdbe.org/5rfa PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5rfa RCSB], [http://www.ebi.ac.uk/pdbsum/5rfa PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5rfa ProSAT]</span></td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene>, <scene name='pdbligand=JGY:1-methyl-N-{[(2S)-oxolan-2-yl]methyl}-1H-pyrazole-3-carboxamide'>JGY</scene></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=5rfa FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5rfa OCA], [https://pdbe.org/5rfa PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5rfa RCSB], [https://www.ebi.ac.uk/pdbsum/5rfa PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5rfa ProSAT]</span></td></tr>
</table>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
COVID-19, caused by SARS-CoV-2, lacks effective therapeutics. Additionally, no antiviral drugs or vaccines were developed against the closely related coronavirus, SARS-CoV-1 or MERS-CoV, despite previous zoonotic outbreaks. To identify starting points for such therapeutics, we performed a large-scale screen of electrophile and non-covalent fragments through a combined mass spectrometry and X-ray approach against the SARS-CoV-2 main protease, one of two cysteine viral proteases essential for viral replication. Our crystallographic screen identified 71 hits that span the entire active site, as well as 3 hits at the dimer interface. These structures reveal routes to rapidly develop more potent inhibitors through merging of covalent and non-covalent fragment hits; one series of low-reactivity, tractable covalent fragments were progressed to discover improved binders. These combined hits offer unprecedented structural and reactivity information for on-going structure-based drug design against SARS-CoV-2 main protease.
Crystallographic and electrophilic fragment screening of the SARS-CoV-2 main protease.,Douangamath A, Fearon D, Gehrtz P, Krojer T, Lukacik P, Owen CD, Resnick E, Strain-Damerell C, Aimon A, Abranyi-Balogh P, Brandao-Neto J, Carbery A, Davison G, Dias A, Downes TD, Dunnett L, Fairhead M, Firth JD, Jones SP, Keeley A, Keseru GM, Klein HF, Martin MP, Noble MEM, O'Brien P, Powell A, Reddi RN, Skyner R, Snee M, Waring MJ, Wild C, London N, von Delft F, Walsh MA Nat Commun. 2020 Oct 7;11(1):5047. doi: 10.1038/s41467-020-18709-w. PMID:33028810<ref>PMID:33028810</ref>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
<div class="pdbe-citations 5rfa" style="background-color:#fffaf0;"></div>
==See Also==
*[[Virus protease 3D structures|Virus protease 3D structures]]
== References ==
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Aimon, A]]
[[Category: Aimon A]]
[[Category: Brandao-Neto, J]]
[[Category: Brandao-Neto J]]
[[Category: Carbery, A]]
[[Category: Carbery A]]
[[Category: Delft, F von]]
[[Category: Douangamath A]]
[[Category: Douangamath, A]]
[[Category: Dunnett L]]
[[Category: Dunnett, L]]
[[Category: Fearon D]]
[[Category: Fearon, D]]
[[Category: Gehrtz P]]
[[Category: Gehrtz, P]]
[[Category: Krojer T]]
[[Category: Krojer, T]]
[[Category: London N]]
[[Category: London, N]]
[[Category: Lukacik P]]
[[Category: Lukacik, P]]
[[Category: Owen CD]]
[[Category: Owen, C D]]
[[Category: Powell AJ]]
[[Category: Powell, A J]]
[[Category: Resnick E]]
[[Category: Resnick, E]]
[[Category: Skyner R]]
[[Category: Skyner, R]]
[[Category: Snee M]]
[[Category: Snee, M]]
[[Category: Strain-Damerell CM]]
[[Category: Strain-Damerell, C M]]
[[Category: Walsh MA]]
[[Category: Walsh, M A]]
[[Category: Wild C]]
[[Category: Wild, C]]
[[Category: Von Delft F]]
[[Category: Hydrolase-hydrolase inhibitor complex]]
[[Category: Pandda]]
[[Category: Sgc - diamond i04-1 fragment screening]]
[[Category: Xchemexplorer]]

Latest revision as of 13:24, 18 February 2026

PanDDA analysis group deposition -- Crystal Structure of SARS-CoV-2 main protease in complex with Z2643472210

5rfa, resolution 1.52Å

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