6KLG
Crystal Structure of the Zea Mays laccase 3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17B1 |
Synchrotron site | SSRF |
Beamline | BL17B1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2019-05-14 |
Detector | RAYONIX MX-300 |
Wavelength(s) | 1.03317 |
Spacegroup name | P 61 2 2 |
Unit cell lengths | 111.977, 111.977, 208.094 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 29.484 - 2.100 |
R-factor | 0.1656 |
Rwork | 0.164 |
R-free | 0.20010 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1aoz |
RMSD bond length | 0.008 |
RMSD bond angle | 0.924 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.140 |
High resolution limit [Å] | 2.100 | 2.100 |
Rmerge | 0.145 | 0.508 |
Number of reflections | 45720 | 2234 |
<I/σ(I)> | 23 | 6.7 |
Completeness [%] | 100.0 | |
Redundancy | 15.6 | |
CC(1/2) | 0.999 | 0.963 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 291 | 15% of PEG 3350, 0.2 M (NH4)2SO4 and 0.1 M Bis-tris,pH 5.5 |