6JWB
Crystal Structures of Endo-beta-1,4-xylanase II Complexed with Xylotriose
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 80 |
Detector technology | CCD |
Collection date | 2018-11-07 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.0 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 48.539, 59.620, 69.714 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.917 - 1.150 |
R-factor | 0.1486 |
Rwork | 0.148 |
R-free | 0.15950 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2dfc |
RMSD bond length | 0.013 |
RMSD bond angle | 1.638 |
Data reduction software | XDS |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX (1.11.1_2575) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.917 | 1.191 |
High resolution limit [Å] | 1.150 | 1.150 |
Number of reflections | 72399 | 7143 |
<I/σ(I)> | 18.41 | |
Completeness [%] | 99.9 | 99.9 |
Redundancy | 6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 6 | 291 | 20%PEG 8000, 0.2M NaI,0.1M MES |