5FO4
Crystal structure of the P.falciparum cytosolic leucyl-tRNA synthetase editing domain (space group P1)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID29 |
Synchrotron site | ESRF |
Beamline | ID29 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2013-09-02 |
Detector | DECTRIS PILATUS 6M |
Spacegroup name | P 1 |
Unit cell lengths | 48.700, 53.400, 63.000 |
Unit cell angles | 88.90, 74.30, 89.70 |
Refinement procedure
Resolution | 60.640 - 1.850 |
R-factor | 0.19737 |
Rwork | 0.195 |
R-free | 0.25214 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PLASMODIUM KNOWLESI LEURS EDITING DOMAIN |
RMSD bond length | 0.015 |
RMSD bond angle | 1.580 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0123) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 15.000 | 2.000 |
High resolution limit [Å] | 1.850 | 1.900 |
Rmerge | 0.060 | 0.520 |
Number of reflections | 45297 | |
<I/σ(I)> | 8.7 | 1.6 |
Completeness [%] | 87.0 | 84 |
Redundancy | 1.8 | 1.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | 0.1 M HEPES (PH 7.5), 10% ISOPROPANOL, 20% (W/V) PEG 4000 AND 5% GLYCEROL |