8K0K
Crystal structure of Csy complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U1 |
Synchrotron site | SSRF |
Beamline | BL17U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-05-01 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.979 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 238.853, 95.077, 204.031 |
Unit cell angles | 90.00, 93.16, 90.00 |
Refinement procedure
Resolution | 46.295 - 2.995 |
R-factor | 0.2 |
Rwork | 0.198 |
R-free | 0.23810 |
Structure solution method | SAD |
RMSD bond length | 0.003 |
RMSD bond angle | 0.650 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX ((1.13_2998: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.100 |
High resolution limit [Å] | 2.995 | 3.000 |
Rmerge | 0.144 | 0.912 |
Number of reflections | 85253 | 6128 |
<I/σ(I)> | 14.9 | |
Completeness [%] | 97.5 | |
Redundancy | 6.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | Sodium acetate |