2WO3
Crystal Structure of the EphA4-ephrinA2 complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I04 |
Synchrotron site | Diamond |
Beamline | I04 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-02-10 |
Detector | ADSC CCD |
Spacegroup name | P 64 |
Unit cell lengths | 115.412, 115.412, 59.354 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 49.970 - 2.350 |
R-factor | 0.20012 |
Rwork | 0.198 |
R-free | 0.24554 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1kgy |
RMSD bond length | 0.011 |
RMSD bond angle | 1.287 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0088) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.410 |
High resolution limit [Å] | 2.350 | 2.350 |
Rmerge | 0.090 | 0.750 |
Number of reflections | 18961 | |
<I/σ(I)> | 30 | 1.8 |
Completeness [%] | 99.9 | 99.4 |
Redundancy | 16 | 8.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8 | 20% PEG 3350, 200 MM KNO3, pH 8.0 |