4K1S
Gly-Ser-SplB protease from Staphylococcus aureus at 1.96 A resolution
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | EMBL/DESY, HAMBURG BEAMLINE BW7A |
Synchrotron site | EMBL/DESY, HAMBURG |
Beamline | BW7A |
Temperature [K] | 100 |
Wavelength(s) | 1.000 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 117.900, 117.900, 73.330 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 22.970 - 1.960 |
R-factor | 0.19468 |
Rwork | 0.192 |
R-free | 0.24676 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2w7s |
RMSD bond length | 0.020 |
RMSD bond angle | 2.042 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 22.970 |
High resolution limit [Å] | 1.960 |
Number of reflections | 32322 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 293 | 0.1M Tris pH 8.5, 25% w/v Polyethylene glycol 3350, VAPOR DIFFUSION, SITTING DROP, temperature 293K |