8F0B
Lysozyme Anomalous Dataset at 240 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] | 240 |
| 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 | 77.106, 77.106, 37.042 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 34.507 - 1.900 |
| Rwork | 0.137 |
| R-free | 0.19810 |
| Structure solution method | SAD |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.475 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | SHELXCD |
| Refinement software | REFMAC (5.8.0352) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 37.040 | 1.940 |
| High resolution limit [Å] | 1.900 | 1.900 |
| Rmerge | 0.053 | 0.169 |
| Rpim | 0.018 | 0.067 |
| Number of reflections | 9246 | 590 |
| <I/σ(I)> | 35.4 | 12.6 |
| Completeness [%] | 100.0 | 100 |
| Redundancy | 15.8 | 12.5 |
| CC(1/2) | 0.999 | 0.993 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 4.5 | 293 | 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. |






