5SWF
The structure of the PP2A B56 subunit double phosphorylated BubR1 complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL12-2 |
Synchrotron site | SSRL |
Beamline | BL12-2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2016-07-09 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 0.98 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 53.307, 107.422, 117.719 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 39.500 - 2.818 |
R-factor | 0.2099 |
Rwork | 0.207 |
R-free | 0.23050 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | 5k6s |
RMSD bond length | 0.002 |
RMSD bond angle | 0.734 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 39.511 | 2.970 |
High resolution limit [Å] | 2.818 | 2.820 |
Rmerge | 0.075 | 0.894 |
Number of reflections | 16683 | |
<I/σ(I)> | 13.5 | 1.8 |
Completeness [%] | 98.7 | 93.8 |
Redundancy | 5.3 | 5.3 |
CC(1/2) | 0.686 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.75 | 298 | 8% PEG 8k, 0.8 M HEPES, 0.8 M LiCl |