5QSL
PanDDA analysis group deposition -- Crystal Structure of human Brachyury in complex with Z1273312153
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I04-1 |
| Synchrotron site | Diamond |
| Beamline | I04-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-07-21 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.91587 |
| Spacegroup name | P 41 2 2 |
| Unit cell lengths | 59.902, 59.902, 109.696 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 52.630 - 2.200 |
| R-factor | 0.2462 |
| Rwork | 0.243 |
| R-free | 0.30500 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 6f58 |
| RMSD bond length | 0.009 |
| RMSD bond angle | 1.615 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.7.1) |
| Phasing software | REFMAC |
| Refinement software | REFMAC (5.8.0238) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 59.900 | 59.900 | 2.010 |
| High resolution limit [Å] | 1.960 | 8.770 | 1.960 |
| Rmerge | 0.198 | 0.077 | 2.595 |
| Rmeas | 0.208 | 0.081 | 2.710 |
| Rpim | 0.061 | 0.024 | 0.773 |
| Total number of observations | 174189 | 2344 | 13140 |
| Number of reflections | 14992 | ||
| <I/σ(I)> | 7.4 | 23.7 | 0.9 |
| Completeness [%] | 99.7 | 99.9 | 99.7 |
| Redundancy | 11.6 | 10.5 | 12.2 |
| CC(1/2) | 0.996 | 0.999 | 0.667 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 4.5 | 298 | 0.1 M CdCl, 0.1 M Acetate pH 4.5, 32% PEG 400 |
