6OE9
Crystal structure of p204 HIN1 domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | NSLS BEAMLINE X25 |
| Synchrotron site | NSLS |
| Beamline | X25 |
| Temperature [K] | 80 |
| Detector technology | PIXEL |
| Collection date | 2011-07-31 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 65 2 2 |
| Unit cell lengths | 58.383, 58.383, 315.836 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 49.925 - 1.940 |
| R-factor | 0.1737 |
| Rwork | 0.172 |
| R-free | 0.19210 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2o0q |
| RMSD bond length | 0.012 |
| RMSD bond angle | 1.325 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 49.920 | 2.010 |
| High resolution limit [Å] | 1.940 | 1.940 |
| Rmerge | 0.082 | 0.334 |
| Rmeas | 0.084 | |
| Number of reflections | 44585 | 2324 |
| <I/σ(I)> | 33.03 | 7.95 |
| Completeness [%] | 98.5 | 95.95 |
| Redundancy | 21.9 | 19.2 |
| CC(1/2) | 0.985 | 0.977 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 293 | 1.33 M ammonium sulfate, 0.05 M sodium acetate pH 4.5, and 0.2 M NaCl |






