5HX5
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 | 35.940, 50.900, 100.860 |
Unit cell angles | 90.00, 90.75, 90.00 |
Refinement procedure
Resolution | 35.937 - 2.330 |
R-factor | 0.2286 |
Rwork | 0.227 |
R-free | 0.26440 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4iou |
RMSD bond length | 0.008 |
RMSD bond angle | 0.602 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((dev_2313: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 35.940 | 2.420 |
High resolution limit [Å] | 2.330 | 2.330 |
Rmerge | 0.117 | |
Number of reflections | 15324 | |
<I/σ(I)> | 6.1 | |
Completeness [%] | 96.8 | |
Redundancy | 3.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 298 | PEG3350, MgCl2 |