1UWW
X-ray crystal structure of a non-crystalline cellulose specific carbohydrate-binding module: CBM28.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-1 |
Synchrotron site | ESRF |
Beamline | ID14-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2002-06-15 |
Detector | ADSC CCD |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 63.866, 65.926, 103.633 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 55.900 - 1.400 |
R-factor | 0.19 |
Rwork | 0.189 |
R-free | 0.20800 |
Structure solution method | SIRAS |
RMSD bond length | 0.017 |
RMSD bond angle | 1.502 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | SOLVE |
Refinement software | REFMAC (5.1.24) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 65.926 | 1.480 |
High resolution limit [Å] | 1.400 | 1.400 |
Rmerge | 0.094 | 0.325 |
Number of reflections | 86838 | |
<I/σ(I)> | 14.4 | 3.4 |
Completeness [%] | 100.0 | 100 |
Redundancy | 6.5 | 4.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 4.6 | 25% (W/V) MONOMETHYL ETHER PEG 2000, 200MM CA-ACETATE, 100MM NA-ACETATE PH 4.6 |