6AXK
Crystal structure of Fab311 complex
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 23-ID-B |
| Synchrotron site | APS |
| Beamline | 23-ID-B |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-03-27 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 1.03320 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 66.117, 44.729, 186.079 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 46.520 - 2.103 |
| R-factor | 0.2053 |
| Rwork | 0.204 |
| R-free | 0.23560 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | homology model |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.663 |
| Data reduction software | HKL-2000 |
| Data scaling software | SCALEPACK |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.11.1_2575: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.520 | 2.140 |
| High resolution limit [Å] | 2.100 | 2.100 |
| Rpim | 0.077 | 0.500 |
| Number of reflections | 32026 | |
| <I/σ(I)> | 11 | |
| Completeness [%] | 98.1 | |
| Redundancy | 5.1 | |
| CC(1/2) | 0.821 | 0.465 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 298 | 0.1M MES pH6.0 36% PEG400 5% PEG3000 |






