6WMB
Crystal structure of a soluble variant of full-length human APOBEC3G (pH 8.0)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-06-28 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 1 |
Spacegroup name | I 1 2 1 |
Unit cell lengths | 60.238, 42.081, 194.210 |
Unit cell angles | 90.00, 95.76, 90.00 |
Refinement procedure
Resolution | 35.230 - 3.020 |
R-factor | 0.2526 |
Rwork | 0.247 |
R-free | 0.30460 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6BUX CHAIN A AND 5K81 CHAIN A |
RMSD bond length | 0.002 |
RMSD bond angle | 0.419 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.000 | 3.210 |
High resolution limit [Å] | 3.020 | 3.020 |
Rmerge | 0.183 | 0.577 |
Number of reflections | 7726 | 367 |
<I/σ(I)> | 5.17 | 1.18 |
Completeness [%] | 84.1 | 79.2 |
Redundancy | 2.7 | 2.1 |
CC(1/2) | 0.942 | 0.498 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8 | 277 | 0.1M Tris (pH 8.0) and 5.5% w/v PEG 4000 |