2hob
From Proteopedia
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|ACTIVITY= | |ACTIVITY= | ||
|GENE= | |GENE= | ||
+ | |DOMAIN= | ||
+ | |RELATEDENTRY= | ||
+ | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2hob FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2hob OCA], [http://www.ebi.ac.uk/pdbsum/2hob PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2hob RCSB]</span> | ||
}} | }} | ||
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[[Category: Yang, H.]] | [[Category: Yang, H.]] | ||
[[Category: Zhao, Q.]] | [[Category: Zhao, Q.]] | ||
- | [[Category: 3IH]] | ||
[[Category: main protease]] | [[Category: main protease]] | ||
[[Category: michael acceptor n3]] | [[Category: michael acceptor n3]] | ||
[[Category: sars-cov]] | [[Category: sars-cov]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 03:33:02 2008'' |
Revision as of 00:33, 31 March 2008
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, resolution 1.95Å | |||||||
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Ligands: | |||||||
Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
Crystal structure of SARS-CoV main protease with authentic N and C-termini in complex with a Michael acceptor N3
Overview
The viral proteases have proven to be the most selective and useful for removing the fusion tags in fusion protein expression systems. As a key enzyme in the viral life-cycle, the main protease (M(pro)) is most attractive for drug design targeting the SARS coronavirus (SARS-CoV), the etiological agent responsible for the outbreak of severe acute respiratory syndrome (SARS) in 2003. In this study, SARS-CoV M(pro) was used to specifically remove the GST tag in a new fusion protein expression system. We report a new method to produce wild-type (WT) SARS-CoV M(pro) with authentic N and C termini, and compare the activity of WT protease with those of three different types of SARS-CoV M(pro) with additional residues at the N or C terminus. Our results show that additional residues at the N terminus, but not at the C terminus, of M(pro) are detrimental to enzyme activity. To explain this, the crystal structures of WT SARS-CoV M(pro) and its complex with a Michael acceptor inhibitor were determined to 1.6 Angstroms and 1.95 Angstroms resolution respectively. These crystal structures reveal that the first residue of this protease is important for sustaining the substrate-binding pocket and inhibitor binding. This study suggests that SARS-CoV M(pro) could serve as a new tag-cleavage endopeptidase for protein overproduction, and the WT SARS-CoV M(pro) is more appropriate for mechanistic characterization and inhibitor design.
About this Structure
2HOB is a Single protein structure of sequence from Sars coronavirus. Full crystallographic information is available from OCA.
Reference
Production of authentic SARS-CoV M(pro) with enhanced activity: application as a novel tag-cleavage endopeptidase for protein overproduction., Xue X, Yang H, Shen W, Zhao Q, Li J, Yang K, Chen C, Jin Y, Bartlam M, Rao Z, J Mol Biol. 2007 Feb 23;366(3):965-75. Epub 2006 Dec 1. PMID:17189639
Page seeded by OCA on Mon Mar 31 03:33:02 2008
Categories: Sars coronavirus | Single protein | Li, J. | Rao, Z. | Shen, W. | Xue, X. | Yang, H. | Zhao, Q. | Main protease | Michael acceptor n3 | Sars-cov