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 |






