2OO6
Crystal structure of putative L-alanine-DL-glutamate epimerase from Burkholderia xenovorans strain LB400
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X29A |
Synchrotron site | NSLS |
Beamline | X29A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-01-20 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.97958 |
Spacegroup name | I 4 2 2 |
Unit cell lengths | 104.906, 104.906, 145.658 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 20.000 - 1.800 |
R-factor | 0.157 |
Rwork | 0.156 |
R-free | 0.19200 |
Structure solution method | SAD |
RMSD bond length | 0.015 |
RMSD bond angle | 1.331 |
Data reduction software | HKL-2000 |
Data scaling software | SCALA |
Phasing software | SHELXD |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 85.130 | 1.900 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.109 | 0.825 |
Total number of observations | 7055 | |
Number of reflections | 35232 | |
<I/σ(I)> | 16.8 | 0.9 |
Completeness [%] | 93.2 | 56.8 |
Redundancy | 8.8 | 2.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 8.5 | 294 | 100mM Tris-HCl pH 8.5, 12% Glycerol, 1.5M Ammonium sulfate, VAPOR DIFFUSION, temperature 294K |