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 |






