5TO7
Structure of the TPR oligomerization domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 21-ID-F |
| Synchrotron site | APS |
| Beamline | 21-ID-F |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2013-03-13 |
| Detector | RAYONIX MX-225 |
| Wavelength(s) | 0.97872 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 164.490, 51.190, 113.800 |
| Unit cell angles | 90.00, 129.32, 90.00 |
Refinement procedure
| Resolution | 44.019 - 2.600 |
| R-factor | 0.2386 |
| Rwork | 0.236 |
| R-free | 0.28090 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5tv5 |
| RMSD bond length | 0.005 |
| RMSD bond angle | 0.733 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 47.490 | 2.530 |
| High resolution limit [Å] | 2.400 | 2.400 |
| Rmerge | 0.130 | 0.825 |
| Number of reflections | 28341 | |
| <I/σ(I)> | 11.2 | 1.3 |
| Completeness [%] | 97.5 | 98.8 |
| Redundancy | 7.4 | 7.5 |
| CC(1/2) | 0.999 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 7.25 | 295 | 28% PEG1K, 0.1M HEPES (7.25) |






