3WPJ
SPATIOTEMPORAL DEVELOPMENT of SOAKED PROTEIN CRYSTAL; NATIVE
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL26B2 |
Synchrotron site | SPring-8 |
Beamline | BL26B2 |
Temperature [K] | 300 |
Detector technology | CCD |
Collection date | 2013-11-26 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 1.07345 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 79.211, 79.211, 37.923 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.000 - 2.000 |
R-factor | 0.16455 |
Rwork | 0.163 |
R-free | 0.20629 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | 2lym |
RMSD bond length | 0.013 |
RMSD bond angle | 1.529 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Refinement software | REFMAC (5.8.0049) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.030 |
High resolution limit [Å] | 2.000 | 2.000 |
Number of reflections | 8605 | |
<I/σ(I)> | 23.1 | 5.9 |
Completeness [%] | 99.6 | 100 |
Redundancy | 6.9 | 7.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | BATCH METHOD | 4.5 | 293 | 25mg/ml Lysozyme, 0.05M SODIUM ACETATE, 0.7M SODIUM CHLORIDE, pH 4.5, BATCH METHOD, temperature 293K |