4D2K
Crystal structure of DREP2 CIDE domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PAL/PLS BEAMLINE 5C (4A) |
Synchrotron site | PAL/PLS |
Beamline | 5C (4A) |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-07-16 |
Detector | ADSC QUANTUM 315r |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 50.283, 88.708, 113.372 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 33.263 - 2.302 |
R-factor | 0.2199 |
Rwork | 0.216 |
R-free | 0.25430 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2eel |
RMSD bond length | 0.009 |
RMSD bond angle | 1.381 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.340 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.010 | 0.280 |
Number of reflections | 22067 | |
<I/σ(I)> | 16.2 | 5.2 |
Completeness [%] | 95.4 | 98.3 |
Redundancy | 9.7 | 5.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 6.2 | 100 MM BIS-TRIS PH6.2, 300 MM MAGNESIUM FORMATE DIHYDRATE |