2QH0
Crystal structure of a glyoxalase from clostridium acetobutylicum
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 | 2007-06-22 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.97920 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 71.100, 71.100, 63.760 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 39.480 - 2.450 |
R-factor | 0.235 |
Rwork | 0.235 |
R-free | 0.29900 |
Structure solution method | SAD |
RMSD bond length | 0.007 |
RMSD bond angle | 1.300 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | SHELX |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.540 |
High resolution limit [Å] | 2.450 | 2.450 |
Rmerge | 0.060 | |
Number of reflections | 6249 | |
<I/σ(I)> | 17.3 | 3.1 |
Completeness [%] | 97.2 | 97.4 |
Redundancy | 24.8 | 20.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293 | HEPES Buffer, pH 7.5, Isopropanol, PEG3350, VAPOR DIFFUSION, SITTING DROP, temperature 293K |