3QU3
Crystal structure of IRF-7 DBD apo form
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X29A |
Synchrotron site | NSLS |
Beamline | X29A |
Temperature [K] | 298 |
Detector technology | CCD |
Collection date | 2008-08-08 |
Detector | ADSC QUANTUM 315 |
Spacegroup name | P 31 |
Unit cell lengths | 68.588, 68.588, 68.610 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 29.700 - 1.300 |
R-factor | 0.169 |
Rwork | 0.161 |
R-free | 0.20000 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2o61 |
RMSD bond length | 0.008 |
RMSD bond angle | 1.029 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.7_650)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.350 |
High resolution limit [Å] | 1.300 | 1.300 |
Rmerge | 0.077 | 0.398 |
Number of reflections | 85736 | |
<I/σ(I)> | 21.3 | 3.4 |
Completeness [%] | 99.8 | 94.2 |
Redundancy | 6.5 | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 293 | 19% PEG 1500, VAPOR DIFFUSION, HANGING DROP, temperature 293K |