8I6I
Crystal structure of cyclohexylamine oxidase from Acinetobacter sp. YT-02
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U1 |
Synchrotron site | SSRF |
Beamline | BL17U1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2019-04-22 |
Detector | MAR CCD 165 mm |
Wavelength(s) | 0.97915 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 109.686, 129.372, 167.385 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 45.910 - 1.490 |
R-factor | 0.16364 |
Rwork | 0.162 |
R-free | 0.18855 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.013 |
RMSD bond angle | 1.810 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0238) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.910 | 1.543 |
High resolution limit [Å] | 1.490 | 1.490 |
Rmeas | 0.022 | 0.351 |
Number of reflections | 173006 | 12624 |
<I/σ(I)> | 21 | 2.4 |
Completeness [%] | 89.5 | |
Redundancy | 2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 293 | 0.1 M sodium citrate (pH 5.5) and 20% PEG1000. |