7SI1
Crystal structure of apo EGFR kinase domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 5.0.1 |
Synchrotron site | ALS |
Beamline | 5.0.1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-10-03 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.97741 |
Spacegroup name | I 2 3 |
Unit cell lengths | 143.536, 143.536, 143.536 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 33.830 - 1.600 |
R-factor | 0.193 |
Rwork | 0.192 |
R-free | 0.21460 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4wrg |
RMSD bond length | 0.010 |
RMSD bond angle | 1.368 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (1.19.2_4158) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 33.830 | 1.657 |
High resolution limit [Å] | 1.600 | 1.600 |
Number of reflections | 64623 | 6455 |
<I/σ(I)> | 33.51 | |
Completeness [%] | 100.0 | 99.97 |
Redundancy | 20.2 | 20.6 |
CC(1/2) | 1.000 | 0.810 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 7 | 292 | 0.1 M MES pH 7.0, 1M Na/K Tartrate |