5J10
De novo design of protein homo-oligomers with modular hydrogen bond network-mediated specificity
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 8.2.2 |
| Synchrotron site | ALS |
| Beamline | 8.2.2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2015-07-09 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 1 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 41.740, 42.120, 123.670 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 61.835 - 2.020 |
| R-factor | 0.2179 |
| Rwork | 0.216 |
| R-free | 0.25170 |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.653 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (dev_1616) |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 61.840 |
| High resolution limit [Å] | 2.020 |
| Number of reflections | 14812 |
| <I/σ(I)> | 14.7 |
| Completeness [%] | 99.2 |
| Redundancy | 6.8 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.1 M Citric acid pH 3.5, 2.0 M Ammonium sulfate |






