5QLK
Group deposition of library data - Crystal Structure of EcDsbA after initial refinement with no ligand modelled (structure C7_1)
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 | 2018-04-18 |
| Detector | ADSC QUANTUM 210r |
| Wavelength(s) | 0.95370 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 118.204, 64.343, 74.591 |
| Unit cell angles | 90.00, 125.78, 90.00 |
Refinement procedure
| Resolution | 34.819 - 1.993 |
| R-factor | 0.2398 |
| Rwork | 0.238 |
| R-free | 0.30430 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.302 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.5.32) |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 47.950 | 47.950 | 2.050 |
| High resolution limit [Å] | 1.990 | 8.910 | 1.990 |
| Rmerge | 0.046 | 0.020 | 0.637 |
| Rmeas | 0.052 | 0.023 | 0.732 |
| Rpim | 0.025 | 0.012 | 0.356 |
| Total number of observations | 128744 | 1335 | 9109 |
| Number of reflections | 31029 | 363 | 2228 |
| <I/σ(I)> | 13.6 | 40.3 | 1.6 |
| Completeness [%] | 99.7 | 97.6 | 97.4 |
| Redundancy | 4.1 | 3.7 | 4.1 |
| CC(1/2) | 0.999 | 0.999 | 0.833 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 6.1 | 293 | 11-13% PEG 8000 5-7.5% GLYCEROL 1 MM CUCL2 100 MM SODIUM CACODYLATE |
