8XIS
Cellodextrin phosphorylase from Clostridium thermocellum mutant - all cysteine residues were substituted with serines
Replaces: 8H2VExperimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE BL-5A |
Synchrotron site | Photon Factory |
Beamline | BL-5A |
Temperature [K] | 95 |
Detector technology | PIXEL |
Collection date | 2021-06-09 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 1.0000 |
Spacegroup name | P 1 |
Unit cell lengths | 82.277, 88.520, 88.540 |
Unit cell angles | 98.41, 110.69, 110.65 |
Refinement procedure
Resolution | 43.440 - 1.680 |
R-factor | 0.1899 |
Rwork | 0.188 |
R-free | 0.22950 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.010 |
RMSD bond angle | 1.083 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHENIX |
Refinement software | PHENIX (1.21rc1_5127) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 43.440 | 1.740 |
High resolution limit [Å] | 1.680 | 1.680 |
Number of reflections | 229962 | 22646 |
<I/σ(I)> | 13.69 | |
Completeness [%] | 97.0 | |
Redundancy | 3.5 | |
CC(1/2) | 1.000 | 0.516 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5 | 293 | 10 mg/ml protein solution was mixed 1:11 with an optimized solution consisting of 100 mM pH 5.0 sodium acetate, 12% PEG4000, and 5% glycerol with streak seeding |