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) |