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2Z3C

A Mechanistic view of Enzyme Inhibition and Peptide Hydrolysis in the Active Site of the SARS-CoV 3C-Like peptidase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 12.3.1
Synchrotron siteALS
Beamline12.3.1
Temperature [K]100
Detector technologyCCD
Collection date2006-07-12
DetectorADSC QUANTUM 315
Wavelength(s)0.97946
Spacegroup nameC 1 2 1
Unit cell lengths108.565, 81.459, 53.359
Unit cell angles90.00, 104.45, 90.00
Refinement procedure
Resolution18.370 - 1.790
R-factor0.19285
Rwork0.190
R-free0.23870
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2a5a
RMSD bond length0.015
RMSD bond angle1.700
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]18.3701.890
High resolution limit [Å]1.7901.790
Rmerge0.0780.643
Number of reflections41831
<I/σ(I)>11.62.7
Completeness [%]98.897.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.529750mM ammonium acetate, 5% polyethylene glycol (Mr10, 000), 3% ethylene glycol, 3% dimethyl sulfoxide, 1mM dithiothreitol, 0.1mM Mes (pH6.5), VAPOR DIFFUSION, HANGING DROP, temperature 297K

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