5HX4
Zinc-Free APOBEC3F Catalytic Domain Crystal Structure
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-E |
Synchrotron site | APS |
Beamline | 24-ID-E |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-07-31 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 36.100, 51.270, 99.770 |
Unit cell angles | 90.00, 90.85, 90.00 |
Refinement procedure
Resolution | 36.096 - 1.920 |
R-factor | 0.1863 |
Rwork | 0.185 |
R-free | 0.21370 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4iou |
RMSD bond length | 0.011 |
RMSD bond angle | 0.951 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((dev_2356: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.910 | 2.000 |
High resolution limit [Å] | 1.920 | 1.920 |
Rmerge | 0.054 | 0.910 |
Number of reflections | 25900 | |
<I/σ(I)> | 13.1 | 0.8 |
Completeness [%] | 96.0 | 62.8 |
Redundancy | 3.2 | 2.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 298 | Tacsimate pH5.0, PEG3350, Glycerol |