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 |