8AXG
Crystal structure of Fusobacterium nucleatum fusolisin protease
This is a non-PDB format compatible entry.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I03 |
Synchrotron site | Diamond |
Beamline | I03 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-02-24 |
Detector | DECTRIS EIGER2 XE 16M |
Wavelength(s) | 0.97625 |
Spacegroup name | P 41 |
Unit cell lengths | 115.475, 115.475, 196.786 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 74.893 - 2.040 |
Rwork | 0.177 |
R-free | 0.21580 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | assembly |
RMSD bond length | 0.006 |
RMSD bond angle | 1.375 |
Data reduction software | DIALS |
Data scaling software | pointless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 75.420 | 2.070 |
High resolution limit [Å] | 2.040 | 2.040 |
Number of reflections | 149218 | 4433 |
<I/σ(I)> | 8.4 | |
Completeness [%] | 91.6 | |
Redundancy | 12.9 | |
CC(1/2) | 0.976 | 0.193 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 297 | 100mM Bis-Tris pH 6.5 and 20% PEG MME5000 |