8EJR
Kelch domain of human KEAP1 bound to Nrf2 linear peptide, Ac-GDPETGE-NH2
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | NSLS-II BEAMLINE 17-ID-2 |
| Synchrotron site | NSLS-II |
| Beamline | 17-ID-2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2021-03-23 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.977 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 162.806, 68.909, 77.586 |
| Unit cell angles | 90.00, 117.66, 90.00 |
Refinement procedure
| Resolution | 29.410 - 2.080 |
| R-factor | 0.2234 |
| Rwork | 0.222 |
| R-free | 0.24860 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5wfv |
| RMSD bond length | 0.009 |
| RMSD bond angle | 1.236 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.17.1_3660) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 29.410 | 2.154 |
| High resolution limit [Å] | 2.080 | 2.080 |
| Rmerge | 0.284 | 0.886 |
| Rmeas | 0.318 | 0.990 |
| Rpim | 0.142 | 0.435 |
| Number of reflections | 45416 | 4519 |
| <I/σ(I)> | 9.9 | 2.1 |
| Completeness [%] | 99.0 | 98.41 |
| Redundancy | 5 | 4.9 |
| CC(1/2) | 0.971 | 0.770 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 290 | 1.6 M ammonium sulfate, 100 mM Bis-Tris pH 6.5, 0.8% PEG monomethyl ether (MME) 550 |






