3SUD
Crystal structure of NS3/4A protease in complex with MK-5172
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-F |
Synchrotron site | APS |
Beamline | 21-ID-F |
Temperature [K] | 100 |
Collection date | 2011-03-31 |
Wavelength(s) | 0.97872 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 56.133, 102.698, 73.289 |
Unit cell angles | 90.00, 112.54, 90.00 |
Refinement procedure
Resolution | 36.480 - 1.960 |
R-factor | 0.18679 |
Rwork | 0.184 |
R-free | 0.23749 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.010 |
RMSD bond angle | 1.429 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Refinement software | REFMAC |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 2.030 |
High resolution limit [Å] | 1.960 | 4.220 | 1.960 |
Rmerge | 0.066 | 0.041 | 0.195 |
Number of reflections | 50198 | ||
<I/σ(I)> | 10 | ||
Completeness [%] | 91.6 | 91.4 | 92.6 |
Redundancy | 2 | 2.4 | 1.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | hanging drop, vapor diffusion | 6.2 | 295 | 20-25% PEG 3350, 0.1M MES (pH 6.5), 4% ammonium sulfate, hanging drop, vapor diffusion, temperature 295K |