1FWN
AQUIFEX AEOLICUS KDO8P SYNTHASE IN COMPLEX WITH PEP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 1999-09-10 |
Detector | RIGAKU RAXIS |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 84.164, 84.164, 159.477 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 25.420 - 1.940 |
R-factor | 0.202 |
Rwork | 0.202 |
R-free | 0.22900 |
RMSD bond length | 0.005 |
RMSD bond angle | 22.500 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Refinement software | CNS (1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.400 | 2.060 |
High resolution limit [Å] | 1.940 | 1.940 |
Rmerge | 0.043 | 0.402 |
Total number of observations | 394602 * | |
Number of reflections | 46302 | |
<I/σ(I)> | 28.6 | |
Completeness [%] | 94.2 | 78.3 |
Redundancy | 8.5 | 4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.8 | 4 * | drop contains protein and reservoir solution in a 1:1 ratio * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | enzyme | 30 (mg/ml) | |
2 | 1 | reservoir | sodium acetate | 100 (mM) | |
3 | 1 | reservoir | PEG4000 | 5-6 (%) |