7D3Y
Crystal structure of the osPHR2-osSPX2 complex
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL17U1 |
| Synchrotron site | SSRF |
| Beamline | BL17U1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-03-18 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9792 |
| Spacegroup name | P 32 2 1 |
| Unit cell lengths | 147.812, 147.812, 143.287 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 48.380 - 3.110 |
| R-factor | 0.2219 |
| Rwork | 0.220 |
| R-free | 0.25260 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 7d3t |
| RMSD bond length | 0.007 |
| RMSD bond angle | 0.563 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.380 | 3.280 |
| High resolution limit [Å] | 3.110 | 3.110 |
| Rmerge | 0.049 | 0.844 |
| Rmeas | 0.051 | 0.865 |
| Rpim | 0.012 | 0.188 |
| Number of reflections | 32993 | 4743 |
| <I/σ(I)> | 35.4 | 4.7 |
| Completeness [%] | 99.9 | |
| Redundancy | 19.8 | |
| CC(1/2) | 0.999 | 0.957 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 291.15 | Ammonium sulfate, Pentaerythritol ethoxylate, Tacsimate |






