2X11
Crystal structure of the complete EphA2 ectodomain in complex with ephrin A5 receptor binding domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID14-2 |
| Synchrotron site | ESRF |
| Beamline | ID14-2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2008-12-13 |
| Detector | ADSC QUANTUM 4 |
| Spacegroup name | P 2 2 21 |
| Unit cell lengths | 173.630, 59.630, 112.160 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 40.482 - 4.830 |
| R-factor | 0.313 |
| Rwork | 0.312 |
| R-free | 0.31430 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | PDB ENTRIES 3CZU 3fl7 1shw |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.675 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 173.000 | 4.900 |
| High resolution limit [Å] | 4.800 | 4.800 |
| Rmerge | 0.110 | 0.740 |
| Number of reflections | 6016 | |
| <I/σ(I)> | 12.95 | 2.8 |
| Completeness [%] | 98.2 | 75.7 |
| Redundancy | 6.2 | 6.2 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | TWO PARTS OF PROTEIN SOLUTION WERE MIXED WITH ONE PART WATER, ONE PART RESERVOIR SOLUTION (8 % POLYETHYLENE GLYCOL 6000, 0.8 M LICL, 0.08 M CITRATE PH 5) AND ONE PART 1 % POLYVINYLPYRROLIDONE K15. |






