6O7B
Crystal structure of Csm1-Csm4 cassette in complex with cA4
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-E |
Synchrotron site | APS |
Beamline | 24-ID-E |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-11-28 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.9791 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 156.578, 156.578, 187.087 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 49.480 - 2.400 |
R-factor | 0.22646 |
Rwork | 0.222 |
R-free | 0.27118 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6mua |
RMSD bond length | 0.005 |
RMSD bond angle | 1.527 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | REFMAC (5.8.0238) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.490 |
High resolution limit [Å] | 2.400 | 2.400 |
Rpim | 0.025 | |
Number of reflections | 52979 | 5181 |
<I/σ(I)> | 27.7 | |
Completeness [%] | 99.9 | |
Redundancy | 37.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.2 | 293 | 0.1 M phosphate-citrate pH 4.2, 5% PEG3000, 25% 1,2-propanediol, and 10% glycerol |