1JDF
Glucarate Dehydratase from E.coli N341D mutant
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 113 |
Detector technology | CCD |
Collection date | 1999-12-01 |
Detector | CUSTOM-MADE |
Spacegroup name | P 1 |
Unit cell lengths | 70.925, 83.926, 98.222 |
Unit cell angles | 104.11, 93.75, 113.12 |
Refinement procedure
Resolution | 20.000 - 2.000 |
R-factor | 0.198 |
Rwork | 0.198 |
R-free | 0.23300 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | 1ec8 |
RMSD bond length | 0.006 |
RMSD bond angle | 1.200 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | CNS |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 2.130 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.062 | 0.455 |
Total number of observations | 505535 * | |
Number of reflections | 132888 | |
<I/σ(I)> | 8.6 | |
Completeness [%] | 97.1 | 89 * |
Redundancy | 3.8 | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Microdialysis * | 8 | 4 * | used macroseeding * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | 1 | Tris-HCl | 10 (mM) | |
2 | 1 | 1 | 5 (mM) | ||
3 | 1 | 1 | protein | 13.3 (mg/ml) | |
4 | 1 | 2 | mPEG5000 | 14 (%) | |
5 | 1 | 2 | 50 (mM) | ||
6 | 1 | 2 | 2-propanol | 5 (%) | pH8.0 |
7 | 1 | 2 | HEPPS | 5 (%) |