2OQ6
Crystal structure of JMJD2A complexed with histone H3 peptide trimethylated at Lys9
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-12-21 |
Detector | MARMOSAIC 225 mm CCD |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 101.347, 149.880, 57.260 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.960 - 2.000 |
R-factor | 0.16478 |
Rwork | 0.163 |
R-free | 0.20773 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.013 |
RMSD bond angle | 1.349 |
Data reduction software | MOSFLM |
Data scaling software | CCP4 ((SCALA)) |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.500 | 2.110 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.085 | 0.837 |
Number of reflections | 59834 | |
<I/σ(I)> | 13.5 | 2.1 |
Completeness [%] | 99.9 | 99.7 |
Redundancy | 5.6 | 5.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 5.5 | 277 | 0.1 M citrate, 4mM NiCl2, 20% PEG 3350, VAPOR DIFFUSION, SITTING DROP, temperature 277K, pH 5.50 |