6J4E
Crystal structure of the AtWRKY1 domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL19U1 |
| Synchrotron site | SSRF |
| Beamline | BL19U1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-07-06 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.978 |
| Spacegroup name | P 65 2 2 |
| Unit cell lengths | 99.000, 99.000, 114.333 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 28.579 - 3.126 |
| Rwork | 0.203 |
| R-free | 0.23480 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2ayd |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.115 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.11.1_2575: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 28.580 | 3.238 |
| High resolution limit [Å] | 3.126 | 3.126 |
| Rmerge | 0.165 | 0.581 |
| Rmeas | 0.168 | 0.589 |
| Number of reflections | 6263 | 599 |
| <I/σ(I)> | 16.02 | |
| Completeness [%] | 97.6 | 94.02 |
| Redundancy | 36.8 | 37.5 |
| CC(1/2) | 1.000 | 0.996 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 291 | 0.2M Ammonium sulfate, 0.1M Sodium acetate trihydrate pH 4.6, 30% Polyethylene glycol monomethyl ether 2000 |






