6ZF7
Keap1 kelch domain bound to a small molecule inhibitor of the Keap1-Nrf2 protein-protein interaction
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PETRA III, EMBL c/o DESY BEAMLINE P13 (MX1) |
| Synchrotron site | PETRA III, EMBL c/o DESY |
| Beamline | P13 (MX1) |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-09-27 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.976245 |
| Spacegroup name | P 61 |
| Unit cell lengths | 103.243, 103.243, 55.396 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 51.620 - 1.370 |
| R-factor | 0.1544 |
| Rwork | 0.153 |
| R-free | 0.17970 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5fnu |
| RMSD bond length | 0.008 |
| RMSD bond angle | 1.036 |
| Data reduction software | XDS (v Mar 15, 2019) |
| Data scaling software | autoPROC (1.0.5) |
| Phasing software | PHASER (1.13-2998) |
| Refinement software | PHENIX (1.13_2998) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 51.620 | 1.421 |
| High resolution limit [Å] | 1.370 | 1.372 |
| Rmerge | 0.055 | 0.848 |
| Rmeas | 0.058 | 0.893 |
| Rpim | 0.018 | 0.279 |
| Number of reflections | 138170 | 13844 |
| <I/σ(I)> | 28.64 | 1.95 |
| Completeness [%] | 100.0 | |
| Redundancy | 10.3 | |
| CC(1/2) | 1.000 | 0.826 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 5.6 | 293 | 0.5 M Ammonium sulfate, 0.1 M Sodium citrate tribasic dihydrate pH 5.6 and 1.0 M Lithium sulfate monohydrate |






