6OBN
The crystal structure of coexpressed SDS22:PP1 complex
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | NSLS-II BEAMLINE 17-ID-2 |
| Synchrotron site | NSLS-II |
| Beamline | 17-ID-2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-11-29 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.98 |
| Spacegroup name | P 65 2 2 |
| Unit cell lengths | 94.147, 94.147, 545.819 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 29.870 - 2.700 |
| R-factor | 0.2044 |
| Rwork | 0.202 |
| R-free | 0.24580 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | PDB entries 4MOV & 6HKW |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.771 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHENIX |
| Refinement software | PHENIX ((1.11.1_2575: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 29.870 | 2.810 |
| High resolution limit [Å] | 2.700 | 2.700 |
| Rmerge | 0.203 | 1.623 |
| Number of reflections | 40847 | 4336 |
| <I/σ(I)> | 9 | |
| Completeness [%] | 99.5 | |
| Redundancy | 8.5 | |
| CC(1/2) | 0.997 | 0.652 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 6.2 | 289 | 14% PEG4000, 6% MPD, sodium/potassium phosphate |






