6RY3
Structure of the WUS homeodomain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE MASSIF-3 |
| Synchrotron site | ESRF |
| Beamline | MASSIF-3 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2016-09-25 |
| Detector | DECTRIS EIGER X 4M |
| Wavelength(s) | 0.9677 |
| Spacegroup name | P 41 21 2 |
| Unit cell lengths | 43.120, 43.120, 82.010 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 38.166 - 1.374 |
| R-factor | 0.1859 |
| Rwork | 0.184 |
| R-free | 0.21300 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3hdd |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.047 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.12_2829) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 38.170 | 1.423 |
| High resolution limit [Å] | 1.374 | 1.374 |
| Rmerge | 0.038 | |
| Rpim | 0.008 | 0.030 |
| Number of reflections | 16816 | 1628 |
| <I/σ(I)> | 61.11 | |
| Completeness [%] | 99.8 | |
| Redundancy | 24.5 | |
| CC(1/2) | 0.999 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 291 | 2.5 M ammonium sulfate 0.05 M MES (pH 6.0) 0.01 M magnesium acetate |






