5GPR
Crystal structure of chitinase-h from Ostrinia furnacalis
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-07-08 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.97861 |
Spacegroup name | P 2 21 21 |
Unit cell lengths | 48.908, 114.419, 122.639 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 44.972 - 3.230 |
R-factor | 0.2161 |
Rwork | 0.211 |
R-free | 0.25650 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3w4r |
RMSD bond length | 0.005 |
RMSD bond angle | 0.800 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 50.000 |
High resolution limit [Å] | 3.230 |
Number of reflections | 12123 |
<I/σ(I)> | 8.94 |
Completeness [%] | 100.0 |
Redundancy | 11.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 277.15 | 0.1M HEPES pH 7.0, 30% v/v Jeffamine ED-2001, pH 7.0 |