5FLJ
enzyme-substrate-dioxygen complex of Ni-quercetinase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Detector | MARMOSAIC 225 mm CCD |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 102.812, 114.586, 105.990 |
Unit cell angles | 90.00, 95.61, 90.00 |
Refinement procedure
Resolution | 38.803 - 1.818 |
R-factor | 0.1662 |
Rwork | 0.164 |
R-free | 0.20760 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5flh |
RMSD bond length | 0.010 |
RMSD bond angle | 1.181 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.910 | 1.960 |
High resolution limit [Å] | 1.820 | 1.820 |
Rmerge | 0.050 | 0.790 |
Number of reflections | 210593 | |
<I/σ(I)> | 14.3 | |
Completeness [%] | 96.4 | 91.1 |
Redundancy | 3.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8 | 0.1 M CACL2, 0.1 M TRIS-HCL PH 8.0, 10 - 13% PEG6000 AND 5% GLYCEROL |