7W3O
Crystal structure of human CYB5R3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL32XU |
Synchrotron site | SPring-8 |
Beamline | BL32XU |
Temperature [K] | 95 |
Detector technology | PIXEL |
Collection date | 2020-02-05 |
Detector | DECTRIS EIGER X 9M |
Wavelength(s) | 1.0000 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 163.360, 79.920, 169.400 |
Unit cell angles | 90.00, 98.72, 90.00 |
Refinement procedure
Resolution | 49.569 - 2.460 |
R-factor | 0.2327 |
Rwork | 0.231 |
R-free | 0.25950 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3w5h |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHENIX |
Refinement software | PHENIX (1.13_2998) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.569 | 2.610 |
High resolution limit [Å] | 2.460 | 2.460 |
Rmerge | 0.259 | 1.780 |
Number of reflections | 78626 | 2536 |
<I/σ(I)> | 12.5 | |
Completeness [%] | 100.0 | |
Redundancy | 12.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 30% PEG 1500, 10% 2-propanol, 0.1M bicine at pH 8.5 |