3CZU
Crystal structure of the human ephrin A2- ephrin A1 complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU FR-E+ SUPERBRIGHT |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2008-03-10 |
Detector | RIGAKU RAXIS IV |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 99.431, 99.431, 204.879 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 24.860 - 2.650 |
R-factor | 0.19507 |
Rwork | 0.193 |
R-free | 0.22533 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB ENTRIES 3C8X 1shw |
RMSD bond length | 0.009 |
RMSD bond angle | 1.225 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.000 | 2.740 |
High resolution limit [Å] | 2.650 | 2.650 |
Number of reflections | 18122 | |
<I/σ(I)> | 35.74 | 5.509 |
Completeness [%] | 100.0 | 100 |
Redundancy | 20.8 | 21.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 5.6 | 290.9 | 14.9% PEG 4000, 0.1M Sodium citrate pH 5.6, 20% Isopropanol, VAPOR DIFFUSION, HANGING DROP, temperature 290.9K, pH 5.60 |