5F07
Crystal structure of glutathione transferase F8 from Populus trichocarpa
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM30A |
Synchrotron site | ESRF |
Beamline | BM30A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-06-17 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.979769 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 90.010, 55.290, 55.029 |
Unit cell angles | 90.00, 119.89, 90.00 |
Refinement procedure
Resolution | 39.017 - 1.500 |
R-factor | 0.1654 |
Rwork | 0.164 |
R-free | 0.18810 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4ri6 |
RMSD bond length | 0.008 |
RMSD bond angle | 1.182 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | MOLREP |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.710 | 1.580 |
High resolution limit [Å] | 1.500 | 1.500 |
Rmerge | 0.045 | 0.292 |
Number of reflections | 37437 | |
<I/σ(I)> | 14.9 | 3.5 |
Completeness [%] | 99.6 | 98.4 |
Redundancy | 3.6 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | MICROBATCH | 6.5 | 277 | 25% PEG 4000, Na MES pH6.5, 0.2 M Mg chloride |