8EZO
Lysozyme Anomalous Dataset at 220 K and 7.1 keV
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRL BEAMLINE BL14-1 |
| Synchrotron site | SSRL |
| Beamline | BL14-1 |
| Temperature [K] | 220 |
| Detector technology | PIXEL |
| Collection date | 2020-01-19 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 1.7462 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 76.909, 76.909, 36.961 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 38.484 - 1.900 |
| Rwork | 0.156 |
| R-free | 0.19130 |
| Structure solution method | SAD |
| RMSD bond length | 0.009 |
| RMSD bond angle | 1.633 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | SHELXDE |
| Refinement software | REFMAC (5.8.0352) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 38.484 | 1.940 |
| High resolution limit [Å] | 1.900 | 1.900 |
| Rmerge | 0.046 | 0.251 |
| Rpim | 0.015 | 0.102 |
| Number of reflections | 9211 | 580 |
| <I/σ(I)> | 37.2 | 8.5 |
| Completeness [%] | 99.9 | 98.2 |
| Redundancy | 15.6 | 11.6 |
| CC(1/2) | 0.999 | 0.992 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 4.5 | 298 | 5 uL of 0.6 M Sodium Chloride in 100 mM Sodium Acetate buffer pH 4.5 and 25% ethylene glycol were mixed with 5 uL 100 mg/mL lysozyme in 100 mM Sodium Acetate. |






