3LJW
Crystal Structure of the Second Bromodomain of Human Polybromo
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X4C |
Synchrotron site | NSLS |
Beamline | X4C |
Temperature [K] | 298 |
Detector technology | CCD |
Collection date | 2009-06-12 |
Detector | MAR CCD 130 mm |
Wavelength(s) | 0.97854 |
Spacegroup name | P 31 |
Unit cell lengths | 78.964, 78.964, 50.651 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 28.340 - 1.501 |
R-factor | 0.1735 |
Rwork | 0.173 |
R-free | 0.19650 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3g0j |
RMSD bond length | 0.006 |
RMSD bond angle | 0.927 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | SOLVE |
Refinement software | PHENIX ((phenix.refine: 1.5_2)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.570 |
High resolution limit [Å] | 1.455 | 1.510 |
Number of reflections | 59763 | 6101 |
<I/σ(I)> | 35.4 | 6.17 |
Completeness [%] | 98.8 | 99.9 |
Redundancy | 3.7 | 3.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5.5 | 298 | 35% PEG 4000, 10 mM Sodium Acetate, pH 5.5, VAPOR DIFFUSION, SITTING DROP, temperature 298K |