6A1C
Crystal structure of the CK2a1-go289 complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL44XU |
Synchrotron site | SPring-8 |
Beamline | BL44XU |
Temperature [K] | 95 |
Detector technology | CCD |
Collection date | 2015-04-18 |
Detector | RAYONIX MX300HE |
Wavelength(s) | 0.9 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 51.657, 78.831, 79.403 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 55.940 - 1.680 |
R-factor | 0.14042 |
Rwork | 0.138 |
R-free | 0.19627 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3war |
RMSD bond length | 0.018 |
RMSD bond angle | 1.921 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0069) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 55.950 | 1.710 |
High resolution limit [Å] | 1.680 | 1.680 |
Rmerge | 0.056 | 0.462 |
Number of reflections | 37267 | |
<I/σ(I)> | 30.6 | 5.7 |
Completeness [%] | 99.6 | 99.3 |
Redundancy | 7.3 | 7.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 277 | ethyleneglycol |