1GNX
b-glucosidase from Streptomyces sp
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | EMBL/DESY, HAMBURG BEAMLINE BW7A |
Synchrotron site | EMBL/DESY, HAMBURG |
Beamline | BW7A |
Temperature [K] | 103 |
Detector technology | IMAGE PLATE |
Detector | MARRESEARCH |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 96.700, 111.280, 185.310 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 40.000 - 1.680 |
R-factor | 0.19 |
Rwork | 0.190 |
R-free | 0.21000 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1cbg |
RMSD bond length | 0.005 |
RMSD bond angle | 1.372 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | AMoRE |
Refinement software | CNS (1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.000 | 1.720 |
High resolution limit [Å] | 1.690 | 1.690 |
Rmerge | 0.038 | 0.232 |
Number of reflections | 108818 | |
<I/σ(I)> | 34.3 | 5.86 |
Completeness [%] | 97.7 | 68.4 |
Redundancy | 85.6 | 74.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | 1.9 M AMMOMIUM SULFATE, 0.1 M HEPES PH 7.5 |