1H4G
Oligosaccharide-binding to family 11 xylanases: both covalent intermediate and mutant-product complexes display 2,5B conformations at the active-centre
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | EMBL/DESY, HAMBURG BEAMLINE BW7B |
Synchrotron site | EMBL/DESY, HAMBURG |
Beamline | BW7B |
Temperature [K] | 120 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 72.061, 75.098, 78.270 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 20.000 - 1.100 |
R-factor | 0.158 * |
Rwork | 0.158 |
R-free | 0.18000 * |
Structure solution method | OTHER |
RMSD bond length | 0.016 * |
RMSD bond angle | 0.039 * |
Data scaling software | SCALEPACK |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 1.120 |
High resolution limit [Å] | 1.100 | 1.100 |
Rmerge | 0.055 * | 0.710 * |
Number of reflections | 171783 | |
<I/σ(I)> | 17.6 | 2 |
Completeness [%] | 99.9 * | 99 |
Redundancy | 4.5 | 3.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 6 | DROP: 2UL PROTEIN (10 MG ML-1 IN 100MM SODIUM ACETATE) PLUS 1UL RESERVOIR RESERVOIR: 100 MM MES PH 6.5, 30% AMMONIUM SULPHATE |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 10 (mg/ml) | |
2 | 1 | drop | sodium acetate | 100 (mM) | pH6.0 |
3 | 1 | reservoir | MES | 100 (mM) | |
4 | 1 | reservoir | ammonium sulfate | 30 (%) | pH6.5 |
5 | 1 | reservoir | 100 (mM) |