6KVV
Crystal Structure Analysis of Endo-beta-1,4-xylanase II Complexed with Xylotriose
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 77 |
Detector technology | CCD |
Collection date | 2019-06-02 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.0 |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 66.679, 67.931, 78.810 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.839 - 1.190 |
R-factor | 0.1499 |
Rwork | 0.150 |
R-free | 0.15940 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2dfc |
RMSD bond length | 0.016 |
RMSD bond angle | 2.027 |
Data reduction software | XDS |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX (1.12_2829) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.840 | 1.264 |
High resolution limit [Å] | 1.190 | 1.190 |
Rmerge | 0.910 | 0.910 |
Number of reflections | 56607 | 5303 |
<I/σ(I)> | 8.24 | |
Completeness [%] | 98.3 | |
Redundancy | 1.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 4.5 | 291 | PEG 8000, NaI, NaAc-HAc |