5K6S
The structure of the PP2A B56 subunit 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 | 2016-03-19 |
| Detector | DECTRIS PILATUS3 6M |
| Wavelength(s) | 0.98 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 53.231, 107.811, 117.998 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 39.522 - 2.794 |
| R-factor | 0.2013 |
| Rwork | 0.198 |
| R-free | 0.22680 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2jak |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.686 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.5.17) |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 39.520 | 2.940 |
| High resolution limit [Å] | 2.790 | 2.790 |
| Rmerge | 0.072 | 1.382 |
| Number of reflections | 17235 | |
| <I/σ(I)> | 16.8 | |
| Completeness [%] | 98.4 | 93.2 |
| Redundancy | 6.6 | 6.7 |
| CC(1/2) | 0.999 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.75 | 298 | 8% PEG 6K, 0.8 M HEPES, 0.8 M LiCl |






