6JKK
Crystal structure of BubR1 kinase domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU MICROMAX-007 HF |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-10-09 |
Detector | RIGAKU SATURN 944+ |
Wavelength(s) | 1.54178 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 59.221, 61.617, 94.054 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 26.689 - 1.850 |
R-factor | 0.1894 |
Rwork | 0.188 |
R-free | 0.22090 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4r8q |
RMSD bond length | 0.005 |
RMSD bond angle | 0.955 |
Data reduction software | DENZO |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.8.2_1309) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 1.890 |
High resolution limit [Å] | 1.850 | 4.850 | 1.850 |
Rmerge | 0.071 | 0.041 | 0.610 |
Number of reflections | 29503 | 1821 | 1336 |
<I/σ(I)> | 9.6 | ||
Completeness [%] | 98.0 | 99.1 | 82 |
Redundancy | 6.5 | 6.5 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 289 | 4% PEG 3000, 0.1M Bis-tris propane pH 7.5 |