5K2L
Crystal structure of LysM domain from Volvox carteri chitinase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE BL-17A |
Synchrotron site | Photon Factory |
Beamline | BL-17A |
Temperature [K] | 95 |
Detector technology | PIXEL |
Collection date | 2014-11-02 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.98 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 29.130, 29.130, 94.257 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 27.830 - 1.200 |
R-factor | 0.14073 |
Rwork | 0.139 |
R-free | 0.17959 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4pxv |
RMSD bond length | 0.026 |
RMSD bond angle | 1.999 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0049) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.220 |
High resolution limit [Å] | 1.200 | 1.200 |
Number of reflections | 13481 | |
<I/σ(I)> | 73 | |
Completeness [%] | 99.5 | |
Redundancy | 23.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.2 M Sodium citrate tribasic dihydrate, 20 % PEG 3350 |