8Y7F
Crystal structure of CARF domain-truncated Csx1-Crn2 from Marinitoga sp.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL02U1 |
Synchrotron site | SSRF |
Beamline | BL02U1 |
Temperature [K] | 80 |
Detector technology | PIXEL |
Collection date | 2023-10-14 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.979 |
Spacegroup name | P 43 3 2 |
Unit cell lengths | 210.580, 210.580, 210.580 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 40.530 - 2.950 |
R-factor | 0.2014 |
Rwork | 0.200 |
R-free | 0.23020 |
Structure solution method | SAD |
RMSD bond length | 0.011 |
RMSD bond angle | 1.301 |
Data reduction software | xia2 |
Data scaling software | xia2 |
Phasing software | PHENIX |
Refinement software | PHENIX ((1.20.1_4487: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.530 | 3.060 |
High resolution limit [Å] | 2.950 | 2.950 |
Number of reflections | 34091 | 34091 |
<I/σ(I)> | 19.7 | |
Completeness [%] | 100.0 | |
Redundancy | 39.7 | |
CC(1/2) | 0.999 | 1.000 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 298 | 0.2 M Calcium acetate,0.1 M Na cacodylate pH 6.5, 40% PEG 300 |