2ITZ
Crystal structure of EGFR kinase domain L858R mutation in complex with Iressa
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-C |
Synchrotron site | APS |
Beamline | 24-ID-C |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-07-21 |
Detector | ADSC QUANTUM 315 |
Spacegroup name | I 2 3 |
Unit cell lengths | 145.929, 145.929, 145.929 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 25.000 - 2.800 |
R-factor | 0.205 |
Rwork | 0.202 |
R-free | 0.25500 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1m17 |
RMSD bond length | 0.015 |
RMSD bond angle | 1.631 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.020 |
High resolution limit [Å] | 2.800 | 2.800 |
Rmerge | 0.060 | 0.330 |
Number of reflections | 12826 | |
<I/σ(I)> | 22.5 | 3.3 |
Completeness [%] | 93.9 | 85.3 |
Redundancy | 4.9 | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | 40% PEG400, 0.15M NACL, 0.1M HEPES PH7.5, pH 7.50 |