5QRS
PanDDA analysis group deposition -- Crystal Structure of human Brachyury in complex with Z1891773393
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 | 59.871, 59.871, 110.259 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 59.870 - 2.060 |
| R-factor | 0.2156 |
| Rwork | 0.213 |
| R-free | 0.26050 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 6f58 |
| RMSD bond length | 0.006 |
| RMSD bond angle | 1.450 |
| 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] | 110.250 | 110.250 | 2.110 |
| High resolution limit [Å] | 2.060 | 9.210 | 2.060 |
| Rmerge | 0.428 | 0.076 | 5.119 |
| Rmeas | 0.448 | 0.081 | 5.370 |
| Rpim | 0.129 | 0.027 | 1.605 |
| Total number of observations | 156038 | 2043 | 10508 |
| Number of reflections | 13075 | ||
| <I/σ(I)> | 10.3 | 21.9 | 2.8 |
| Completeness [%] | 100.0 | 99.9 | 100 |
| Redundancy | 11.9 | 10.2 | 11.3 |
| CC(1/2) | 0.989 | 0.984 | 0.467 |
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 |
