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2alv

From Proteopedia

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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2alv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2alv OCA], [http://www.ebi.ac.uk/pdbsum/2alv PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2alv RCSB]</span>
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[[Category: Santarsiero, B D.]]
[[Category: Santarsiero, B D.]]
[[Category: Xi, K.]]
[[Category: Xi, K.]]
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[[Category: CY6]]
 
[[Category: 3c]]
[[Category: 3c]]
[[Category: 3cl]]
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[[Category: sar]]
[[Category: sar]]
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Revision as of 22:54, 30 March 2008


PDB ID 2alv

Drag the structure with the mouse to rotate
, resolution 1.90Å
Ligands:
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



X-ray structural analysis of SARS coronavirus 3CL proteinase in complex with designed anti-viral inhibitors


Overview

Design, synthesis, and biological evaluation of peptidomimetic severe acute respiratory syndrome chymotrypsin-like protease (SARS-3CLpro) inhibitors for severe acute respiratory syndrome coronavirus (SARS-CoV) are described. These inhibitors exhibited antiviral activity against SARS-CoV in infected cells in the micromolar range. An X-ray crystal structure of our lead inhibitor (4) bound to SARS-3CLpro provided important drug-design templates for the design of small-molecule inhibitors.

About this Structure

2ALV is a Single protein structure of sequence from Human sars coronavirus. Full crystallographic information is available from OCA.

Reference

Design and synthesis of peptidomimetic severe acute respiratory syndrome chymotrypsin-like protease inhibitors., Ghosh AK, Xi K, Ratia K, Santarsiero BD, Fu W, Harcourt BH, Rota PA, Baker SC, Johnson ME, Mesecar AD, J Med Chem. 2005 Nov 3;48(22):6767-71. PMID:16250632

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