7EOX
Protease structure from Euphorbia resinifera
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SPRING-8 BEAMLINE BL44XU |
| Synchrotron site | SPring-8 |
| Beamline | BL44XU |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-11-28 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.90000 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 67.673, 112.880, 201.801 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 60.010 - 1.700 |
| R-factor | 0.20434 |
| Rwork | 0.203 |
| R-free | 0.23667 |
| Structure solution method | SAD |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.621 |
| Data reduction software | DIALS |
| Data scaling software | DIALS |
| Phasing software | HKL2Map |
| Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 64.160 | 64.160 | 1.730 |
| High resolution limit [Å] | 1.700 | 9.310 | 1.700 |
| Rmerge | 0.116 | 0.031 | 2.683 |
| Rmeas | 0.141 | 0.038 | 3.278 |
| Rpim | 0.080 | 0.021 | 1.853 |
| Number of reflections | 168106 | 1029 | 8027 |
| <I/σ(I)> | 9.7 | ||
| Completeness [%] | 99.0 | ||
| Redundancy | 5.8 | 5.8 | 6 |
| CC(1/2) | 0.995 | 0.972 | 0.520 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 291 | 0.2M sodium idodide (0.2 M), 0.1M Bis-Tris propane pH 8.5, 20% W/V PEG 3350 |






