5TO5
Structure of the TPR oligomerization domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 21-ID-D |
| Synchrotron site | APS |
| Beamline | 21-ID-D |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2013-03-16 |
| Detector | RAYONIX MX300-HS |
| Wavelength(s) | 1.07812 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 74.177, 51.551, 94.980 |
| Unit cell angles | 90.00, 107.83, 90.00 |
Refinement procedure
| Resolution | 21.411 - 2.500 |
| R-factor | 0.2318 |
| Rwork | 0.229 |
| R-free | 0.28200 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.722 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 21.850 |
| High resolution limit [Å] | 2.180 |
| Rmerge | 0.079 |
| Number of reflections | 17251 |
| <I/σ(I)> | 15.8 |
| Completeness [%] | 96.0 |
| Redundancy | 5.7 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 6.25 | 295 | 16% PEG1.5K, 0.1M Bistris (6.25) |






