5ZX1
Crystal structure of ENT domain from T. brucei
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U1 |
Synchrotron site | SSRF |
Beamline | BL17U1 |
Temperature [K] | 293 |
Detector technology | PIXEL |
Collection date | 2018-05-12 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9791 |
Spacegroup name | I 41 2 2 |
Unit cell lengths | 132.590, 132.590, 40.030 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 46.878 - 2.310 |
Rwork | 0.234 |
R-free | 0.27880 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1uz3 |
Data reduction software | xia2 |
Data scaling software | xia2 |
Phasing software | PHENIX (1.13-2998) |
Refinement software | PHENIX (1.13-2998) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.880 | 2.390 |
High resolution limit [Å] | 2.310 | 2.310 |
Rmerge | 0.028 | 0.270 |
Rpim | 0.028 | |
Number of reflections | 8072 | 1586 |
<I/σ(I)> | 14.5 | |
Completeness [%] | 99.0 | |
Redundancy | 12.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 292 | 0.2M L-proline, 0.1M HEPES pH7.5, 10% PEG 3350 |