4L22
Crystal structure of putative glycogen phosphorylase from Streptococcus mutans
Experimental procedure
| Experimental method | MAD |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL17U |
| Synchrotron site | SSRF |
| Beamline | BL17U |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2011-01-03 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.979142 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 119.720, 85.020, 84.460 |
| Unit cell angles | 90.00, 93.30, 90.00 |
Refinement procedure
| Resolution | 84.320 - 2.450 |
| R-factor | 0.22385 |
| Rwork | 0.222 |
| R-free | 0.26597 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2c4m |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.119 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Refinement software | REFMAC (5.8.0069) |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 84.320 |
| High resolution limit [Å] | 2.450 |
| Number of reflections | 38983 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Solid-liquid interface method | 8.5 | 289 | 0.2M (NH4)2SO4, 0.1M Tris, 25% PEG3350, pH 8.5, Solid-liquid interface method, temperature 289K |






