2GEF
Crystal structure of a Novel viral protease with a serine/lysine catalytic dyad mechanism
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X26C |
Synchrotron site | NSLS |
Beamline | X26C |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-04-10 |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 0.97804 |
Spacegroup name | I 2 3 |
Unit cell lengths | 144.070, 144.070, 144.070 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.410 - 2.200 |
R-factor | 0.259 |
Rwork | 0.222 |
R-free | 0.26740 |
Structure solution method | SAD |
RMSD bond length | 0.009 |
RMSD bond angle | 1.600 |
Data scaling software | HKL-2000 |
Phasing software | SHARP |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 33.900 | |
High resolution limit [Å] | 2.200 | 2.200 |
Rmerge | 0.059 | |
Number of reflections | 25378 | |
<I/σ(I)> | 76.9 | |
Completeness [%] | 100.0 | 100 |
Redundancy | 16.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 293 | 0.1 M Tris-HCl (pH 8.5), 25% (w/v) PEG2000MME, 60 mM Magnesium acetate, VAPOR DIFFUSION, SITTING DROP, temperature 293K |