1OH3
E78R mutant of a carbohydrate binding module family 29
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 | 38.671, 56.549, 129.770 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 20.000 - 1.500 |
R-factor | 0.171 |
Rwork | 0.170 |
R-free | 0.18700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1gwm |
RMSD bond length | 0.014 |
RMSD bond angle | 1.488 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | AMoRE |
Refinement software | REFMAC (5.1.24) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.631 | 1.580 |
High resolution limit [Å] | 1.500 | 1.500 |
Rmerge | 0.053 | 0.471 |
Number of reflections | 42994 | |
<I/σ(I)> | 16 | 1.8 |
Completeness [%] | 92.6 | 68.4 |
Redundancy | 3.3 | 1.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 6 | 25 % PEG 3350 15 % ETHYLENEGLYCOL, 0.1 M CALCIUM CHLORIDE 5 MM CELLOHEXAOASE, pH 6.00 |