5JMB
The Crystal structure of the N-terminal domain of a novel cellulases from Bacteroides coprocola
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2016-04-22 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.97918 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 47.860, 47.860, 292.850 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 41.000 - 2.050 |
R-factor | 0.1892 |
Rwork | 0.187 |
R-free | 0.23060 |
Structure solution method | SAD |
RMSD bond length | 0.008 |
RMSD bond angle | 1.096 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | HKL-3000 |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.000 | 2.090 |
High resolution limit [Å] | 2.050 | 2.050 |
Rmerge | 0.113 | 0.700 |
Number of reflections | 13622 | |
<I/σ(I)> | 20.7 | 2.4 |
Completeness [%] | 99.7 | 98.1 |
Redundancy | 7.4 | 4.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 289 | 1.8M Ammonium Citrate Tribasic pH7.0 |