2O8L
Structure of V8 protease from staphylococcus aureus
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CLSI BEAMLINE 08ID-1 |
Synchrotron site | CLSI |
Beamline | 08ID-1 |
Detector technology | CCD |
Collection date | 2006-08-04 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 1.3317 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 59.430, 59.430, 214.010 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.370 - 1.500 |
R-factor | 0.1899 |
Rwork | 0.188 |
R-free | 0.21867 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1qy6 |
RMSD bond length | 0.028 |
RMSD bond angle | 2.366 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | AMoRE |
Refinement software | REFMAC (5.2) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.400 | 1.630 |
High resolution limit [Å] | 1.500 | 1.500 |
Rmerge | 0.130 | 0.418 |
Number of reflections | 58412 | |
<I/σ(I)> | 9.95 | 3.2 |
Completeness [%] | 89.8 | 92.3 |
Redundancy | 5.94 | 4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8.6 | 293 | PEG 5000 MME, KCl, HEPES, pH 8.6, VAPOR DIFFUSION, HANGING DROP, temperature 293K |