8F47
Crystal structure of VACV D13 in complex with STK69439
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-08-23 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 0.9537 |
Spacegroup name | P 61 2 2 |
Unit cell lengths | 190.522, 190.522, 257.948 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 26.040 - 3.100 |
R-factor | 0.1709 |
Rwork | 0.168 |
R-free | 0.23190 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6bei |
RMSD bond length | 0.010 |
RMSD bond angle | 1.134 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.20rc4_4425) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.630 | 3.200 |
High resolution limit [Å] | 3.100 | 3.100 |
Number of reflections | 50722 | 4589 |
<I/σ(I)> | 13.1 | 2.6 |
Completeness [%] | 100.0 | 100 |
Redundancy | 22 | |
CC(1/2) | 0.993 | 0.733 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.8 | 293 | 1.7 - 2.2 M sodium formate and 0.1 M citric acid |