5UEQ
BRD4_BD2_A-1390146
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 17-ID |
Synchrotron site | APS |
Beamline | 17-ID |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2011-12-08 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 1.0 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 63.624, 70.417, 33.555 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 35.210 - 1.700 |
R-factor | 0.181 |
Rwork | 0.179 |
R-free | 0.21700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | Apo BRD4 Bromodomain 2 |
RMSD bond length | 0.010 |
RMSD bond angle | 0.940 |
Data reduction software | XDS (2.11.7) |
Data scaling software | SCALA |
Refinement software | BUSTER (2.11.7) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 35.210 |
High resolution limit [Å] | 1.700 |
Number of reflections | 17088 |
<I/σ(I)> | 14.3 |
Completeness [%] | 99.7 |
Redundancy | 6.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 277 | Protein Buffer : 10 mM HEPES PH 7.5 100 mM NaCl 5 mM DTT Crystallization : 15 % (v/v) Ethanol Tris PH 7.0 |