4RLH
Crystal structure of enoyl ACP reductase from Burkholderia pseudomallei in complex with AFN-1252
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU300 |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Detector | RIGAKU RAXIS IV++ |
Wavelength(s) | 1.5416 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 134.795, 63.445, 121.848 |
Unit cell angles | 90.00, 107.08, 90.00 |
Refinement procedure
Resolution | 36.590 - 2.260 |
R-factor | 0.17102 |
Rwork | 0.167 |
R-free | 0.25017 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3ek2 |
RMSD bond length | 0.015 |
RMSD bond angle | 1.855 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | MOLREP |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.330 |
High resolution limit [Å] | 2.250 | 2.250 |
Rmerge | 0.062 | 0.151 |
Number of reflections | 42792 | |
<I/σ(I)> | 11.8 | 2.7 |
Completeness [%] | 93.1 | 89.9 |
Redundancy | 2.7 | 2.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5 | 293 | MES pH 5.0, 0.1 M NaCl, 10% PEG 3350, , VAPOR DIFFUSION, HANGING DROP, temperature 293K |