5DGQ
Crystal structure of GH9 exo-beta-D-glucosaminidase PBPRA0520
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE BL-5A |
Synchrotron site | Photon Factory |
Beamline | BL-5A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-12-20 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.000 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 61.928, 102.318, 90.280 |
Unit cell angles | 90.00, 97.72, 90.00 |
Refinement procedure
Resolution | 31.870 - 1.900 |
R-factor | 0.15972 |
Rwork | 0.157 |
R-free | 0.20625 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3h7l |
RMSD bond length | 0.023 |
RMSD bond angle | 1.978 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0107) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.970 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.100 | 0.289 |
Number of reflections | 87933 | |
<I/σ(I)> | 15.3 | 3.5 |
Completeness [%] | 99.7 | 100 |
Redundancy | 3.7 | 3.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 298 | 10% PEG 6000, 0.1M HEPES-NaOH (pH 7.5), 5% MPD |