8VY5
Crystal structure of human SAE1
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL10U2 |
| Synchrotron site | SSRF |
| Beamline | BL10U2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2024-03-21 |
| Detector | MAR CCD 300 mm |
| Wavelength(s) | 0.97918 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 103.197, 70.187, 87.591 |
| Unit cell angles | 90.00, 108.92, 90.00 |
Refinement procedure
| Resolution | 28.290 - 2.010 |
| R-factor | 0.2327 |
| Rwork | 0.231 |
| R-free | 0.27400 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.231 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 56.990 | 2.120 |
| High resolution limit [Å] | 2.010 | 2.010 |
| Rmerge | 0.053 | 1.141 |
| Rmeas | 0.064 | |
| Rpim | 0.035 | 0.918 |
| Number of reflections | 38233 | 5741 |
| <I/σ(I)> | 13.2 | 1.1 |
| Completeness [%] | 96.4 | |
| Redundancy | 6.1 | |
| CC(1/2) | 0.995 | 0.482 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 291 | Tris 8.5, PEG3350, ammonium acetate NDSB-256 |






