1BQB
AUREOLYSIN, STAPHYLOCOCCUS AUREUS METALLOPROTEINASE
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 284 |
Detector technology | IMAGE PLATE |
Detector | MARRESEARCH |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 33.700, 79.500, 100.100 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 8.000 - 1.720 |
R-factor | 0.176 |
Rwork | 0.176 |
R-free | 0.23900 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1lnf |
RMSD bond length | 0.010 |
RMSD bond angle | 1.380 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | AMoRE |
Refinement software | X-PLOR |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 15.000 | 1.780 |
High resolution limit [Å] | 1.720 | 1.720 |
Rmerge | 0.091 | |
Total number of observations | 120813 * | |
Number of reflections | 27738 | |
<I/σ(I)> | 5.6 | |
Completeness [%] | 93.8 | 86.4 |
Redundancy | 4.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, sitting drop * | 7.6 * | 20 * | 0.1 M SODIUM ACETATE PH 5.2 AND 40% PEG 4000 |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 10 (mg/ml) | |
2 | 1 | drop | Tris-HCl | 10 (mM) | |
3 | 1 | drop | 5 (mM) | ||
4 | 1 | reservoir | sodium acetate | 0.1 (M) | |
5 | 1 | reservoir | PEG4000 | 40 (%) | |
6 | 1 | reservoir | sodium azide | 0.02 (%(w/v)) |