6ZF8
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 | MAX IV BEAMLINE BioMAX |
Synchrotron site | MAX IV |
Beamline | BioMAX |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-12-01 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.976253 |
Spacegroup name | P 61 |
Unit cell lengths | 103.350, 103.350, 55.019 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 44.750 - 1.750 |
R-factor | 0.1469 |
Rwork | 0.146 |
R-free | 0.16960 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5fnu |
RMSD bond length | 0.008 |
RMSD bond angle | 1.030 |
Data reduction software | XDS (v Mar 15, 2019) |
Data scaling software | XDS (v Mar 15, 2019) |
Phasing software | PHASER (1.13-2998) |
Refinement software | PHENIX (1.13_2998) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 44.750 | 1.813 |
High resolution limit [Å] | 1.750 | 1.750 |
Rmerge | 0.061 | 0.148 |
Rmeas | 0.064 | 0.166 |
Rpim | 0.020 | 0.073 |
Number of reflections | 65841 | 6254 |
<I/σ(I)> | 24.17 | 7.26 |
Completeness [%] | 99.4 | 94.54 |
Redundancy | 9.2 | 4.8 |
CC(1/2) | 0.999 | 0.981 |
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 |