28JI
LASV cap-snatching endonuclease, cryo apo structure
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PETRA III, DESY BEAMLINE P11 |
| Synchrotron site | PETRA III, DESY |
| Beamline | P11 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2024-10-17 |
| Detector | DECTRIS EIGER2 X 16M |
| Wavelength(s) | 1.03322 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 57.687, 57.687, 135.551 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 53.080 - 1.610 |
| R-factor | 0.2252 |
| Rwork | 0.224 |
| R-free | 0.23990 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.007 |
| RMSD bond angle | 0.864 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.21.2-5419_9999) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 53.080 | 1.640 |
| High resolution limit [Å] | 1.610 | 1.610 |
| Rmeas | 0.102 | |
| Number of reflections | 30633 | 1501 |
| <I/σ(I)> | 16.9 | 1.3 |
| Completeness [%] | 100.0 | 100 |
| Redundancy | 26.5 | |
| CC(1/2) | 0.999 | 0.807 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | BATCH MODE | 293 | After limited proteolysis with subtilisin A, 7.5 mg/ml protein were mixed with an equal volume of crystallization solution (10% w/v PEG 10000, 250 mM MgSO4 and 100 mM Tris/HCl pH 9.0) |






