Crystal Structures of the Main Peptidase from the SARS Coronavirus Inhibited by a Substrate-like Aza-peptide Epoxide
- 27 September 2005
- journal article
- Published by Elsevier in Journal of Molecular Biology
- Vol. 353 (5) , 1137-1151
- https://doi.org/10.1016/j.jmb.2005.09.004
Abstract
No abstract availableKeywords
Funding Information
- Canadian Institutes of Health Research
- Canada Research Chairs
This publication has 50 references indexed in Scilit:
- On the size of the active site in proteases. I. PapainPublished by Elsevier ,2005
- Irreversible Inhibitors of Serine, Cysteine, and Threonine ProteasesChemical Reviews, 2002
- XtalView/Xfit—A Versatile Program for Manipulating Atomic Coordinates and Electron DensityJournal of Structural Biology, 1999
- Refinement of Macromolecular Structures by the Maximum-Likelihood MethodActa Crystallographica Section D-Biological Crystallography, 1997
- [20] Processing of X-ray diffraction data collected in oscillation modePublished by Elsevier ,1997
- The CCP4 suite: programs for protein crystallographyActa Crystallographica Section D-Biological Crystallography, 1994
- Transient-phase kinetics of enzyme inactivation induced by suicide substratesBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1987
- Phosphocholine binding immunoglobulin Fab McPC603Journal of Molecular Biology, 1986
- Nitrogen-15 nuclear magnetic resonance spectroscopy. The state of histidine in the catalytic triad of .alpha.-lytic protease. Implications for the charge-relay mechanism of peptide-bond cleavage by serine proteasesJournal of the American Chemical Society, 1978
- The detection of sub-units within the crystallographic asymmetric unitActa Crystallographica, 1962