7EIJ
Ancestral L-Lys oxidase K387A variant (L-Arg binding form)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PHOTON FACTORY BEAMLINE AR-NW12A |
| Synchrotron site | Photon Factory |
| Beamline | AR-NW12A |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2020-11-18 |
| Detector | DECTRIS PILATUS3 2M |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 85.932, 80.093, 88.036 |
| Unit cell angles | 90.00, 90.47, 90.00 |
Refinement procedure
| Resolution | 48.900 - 2.200 |
| R-factor | 0.19241 |
| Rwork | 0.190 |
| R-free | 0.23083 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 7eih |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.438 |
| Data reduction software | XDS |
| Data scaling software | SCALA |
| Phasing software | MOLREP |
| Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.900 | 2.320 |
| High resolution limit [Å] | 2.200 | 2.200 |
| Rmerge | 0.084 | 0.446 |
| Number of reflections | 60710 | 8644 |
| <I/σ(I)> | 15.2 | 3.9 |
| Completeness [%] | 99.7 | |
| Redundancy | 6.8 | |
| CC(1/2) | 0.998 | 0.899 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 295 | 25%(w/v) PEG3350, 0.1 M Tris-HCl (pH 8.5) |






