2WPC
Trypanosoma brucei trypanothione reductase in complex with 3,4- dihydroquinazoline inhibitor (DDD00073357)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-1 |
Synchrotron site | ESRF |
Beamline | ID14-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-02-25 |
Detector | ADSC CCD |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 101.250, 63.430, 169.370 |
Unit cell angles | 90.00, 98.58, 90.00 |
Refinement procedure
Resolution | 46.881 - 2.100 |
R-factor | 0.169 |
Rwork | 0.165 |
R-free | 0.23200 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2woi |
RMSD bond length | 0.024 |
RMSD bond angle | 1.964 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | MOLREP |
Refinement software | REFMAC (5.5.0088) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.900 | 2.150 |
High resolution limit [Å] | 2.100 | 2.100 |
Rmerge | 0.110 | 0.380 |
Number of reflections | 117358 | |
<I/σ(I)> | 14.5 | 3.7 |
Completeness [%] | 90.2 | 79.6 |
Redundancy | 3.2 | 3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8 | 15MG/ML PROTEIN IN 25MM HEPES PH 7.5, 50MM NABR EQUILIBRATED AGAINST 24% MPD, 10% PEG 3350, 40MM IMIDAZOLE PH 8.0 |