8IN3
Eisenia hydrolysis-enhancing protein from Aplysia kurodai
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE BL-17A |
Synchrotron site | Photon Factory |
Beamline | BL-17A |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2016-03-12 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.98 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 42.180, 65.330, 66.510 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 35.620 - 1.150 |
R-factor | 0.1823 |
Rwork | 0.182 |
R-free | 0.18920 |
Structure solution method | SAD |
RMSD bond length | 0.005 |
RMSD bond angle | 0.841 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHENIX |
Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.195 |
High resolution limit [Å] | 1.150 | 1.150 |
Number of reflections | 60994 | 4888 |
<I/σ(I)> | 19.28 | |
Completeness [%] | 93.4 | |
Redundancy | 6.6 | |
CC(1/2) | 0.999 | 0.704 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 1.0 M sodium acetate, 0.1 M imidazole (pH 6.5) |