5Q7M
PanDDA analysis group deposition -- Crystal Structure of DCLRE1A after initial refinement with no ligand modelled (structure 195)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I04-1 |
| Synchrotron site | Diamond |
| Beamline | I04-1 |
| Detector technology | PIXEL |
| Collection date | 2017-04-11 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.92 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 51.855, 56.795, 114.893 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 50.910 - 1.260 |
| R-factor | 0.2035 |
| Rwork | 0.202 |
| R-free | 0.22770 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 5aho |
| RMSD bond length | 0.027 |
| RMSD bond angle | 2.246 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.5.31) |
| Phasing software | REFMAC |
| Refinement software | REFMAC (5.8.0155) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.910 | 50.910 | 1.290 |
| High resolution limit [Å] | 1.260 | 5.630 | 1.260 |
| Rmerge | 0.050 | 0.035 | 1.138 |
| Rmeas | 0.055 | 0.038 | 1.319 |
| Rpim | 0.022 | 0.016 | 0.658 |
| Total number of observations | 530521 | 6943 | 25944 |
| Number of reflections | 92342 | ||
| <I/σ(I)> | 12.3 | 43 | 1.2 |
| Completeness [%] | 100.0 | 99.9 | 99.7 |
| Redundancy | 5.7 | 5.9 | 3.9 |
| CC(1/2) | 0.999 | 0.998 | 0.482 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6 | 298 | 30% PEG 1000, 0.1M MIB buffer |
