2XVG
crystal structure of alpha-xylosidase (GH31) from Cellvibrio japonicus
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID29 |
Synchrotron site | ESRF |
Beamline | ID29 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-09-26 |
Detector | ADSC CCD |
Spacegroup name | P 63 2 2 |
Unit cell lengths | 156.193, 156.193, 227.759 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 49.885 - 2.600 |
R-factor | 0.2065 |
Rwork | 0.204 |
R-free | 0.25900 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2g3m |
RMSD bond length | 0.009 |
RMSD bond angle | 1.156 |
Data reduction software | MOSFLM |
Data scaling software | SCALEPACK |
Phasing software | BALBES |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.900 | 2.740 |
High resolution limit [Å] | 2.600 | 2.600 |
Rmerge | 0.110 | 0.810 |
Number of reflections | 50969 | |
<I/σ(I)> | 14.4 | 2.7 |
Completeness [%] | 99.9 | 100 |
Redundancy | 11 | 11.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7 | 25 % PEG MONOMETHYL ETHER 550 (PEG MME 550), 0.1 M BIS-TRIS (PH 7.0) |