6xqu

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(New page: ==Extreme malleability of the SARS-CoV-2 3CL Mpro active site cavity facilitates binding of clinical antivirals: Prospects for repurposing existing drugs and ramifications for inhibitor d...)
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==Extreme malleability of the SARS-CoV-2 3CL Mpro active site cavity facilitates binding of clinical antivirals: Prospects for repurposing existing drugs and ramifications for inhibitor design==
==Extreme malleability of the SARS-CoV-2 3CL Mpro active site cavity facilitates binding of clinical antivirals: Prospects for repurposing existing drugs and ramifications for inhibitor design==
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<StructureSection load='6xqu' size='340' side='right'caption='[[6xqu]]' scene=''>
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<StructureSection load='6xqu' size='340' side='right'caption='[[6xqu]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6XQU OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6XQU FirstGlance]. <br>
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6XQU OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6XQU FirstGlance]. <br>
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6xqu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6xqu OCA], [http://pdbe.org/6xqu PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6xqu RCSB], [http://www.ebi.ac.uk/pdbsum/6xqu PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6xqu ProSAT]</span></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]] 2.2&#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=U5G:boceprevir+(bound+form)'>U5G</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=6xqu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6xqu OCA], [https://pdbe.org/6xqu PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6xqu RCSB], [https://www.ebi.ac.uk/pdbsum/6xqu PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6xqu ProSAT]</span></td></tr>
</table>
</table>
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==See Also==
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*[[Virus protease 3D structures|Virus protease 3D structures]]
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</StructureSection>
</StructureSection>

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Extreme malleability of the SARS-CoV-2 3CL Mpro active site cavity facilitates binding of clinical antivirals: Prospects for repurposing existing drugs and ramifications for inhibitor design

PDB ID 6xqu

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