6PG1
Crystal Structure of EcDsbA in a complex with unpurified reaction product F1 (methylpiperazinone 6)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2018-04-17 |
| Detector | ADSC QUANTUM 210r |
| Wavelength(s) | 0.9537 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 117.996, 64.410, 74.433 |
| Unit cell angles | 90.00, 125.85, 90.00 |
Refinement procedure
| Resolution | 32.210 - 2.010 |
| R-factor | 0.2126 |
| Rwork | 0.211 |
| R-free | 0.26440 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1fvk |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.516 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 47.820 | 2.060 |
| High resolution limit [Å] | 2.000 | 2.000 |
| Rmerge | 0.054 | 0.603 |
| Rmeas | 0.072 | 0.800 |
| Rpim | 0.048 | 0.522 |
| Number of reflections | 30133 | 2125 |
| <I/σ(I)> | 9.7 | 1.3 |
| Completeness [%] | 98.8 | 95 |
| Redundancy | 4.1 | 4 |
| CC(1/2) | 0.999 | 0.782 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 6.1 | 293.15 | 11-13 % PEG 8000, 5-7.5% glycerol, 100mM Na Cacodylate pH6.1, 1mM CuCl2 |
