8DZK
Dbr1 in complex with 5-mer cleavage product
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 24-ID-C |
| Synchrotron site | APS |
| Beamline | 24-ID-C |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2013-10-11 |
| Detector | DECTRIS PILATUS 6M-F |
| Wavelength(s) | 1.0000 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 73.272, 143.341, 214.006 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 50.120 - 2.100 |
| R-factor | 0.1794 |
| Rwork | 0.178 |
| R-free | 0.20920 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 5k73 |
| RMSD bond length | 0.008 |
| RMSD bond angle | 0.999 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Refinement software | PHENIX (1.20_4459) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.120 | 2.175 |
| High resolution limit [Å] | 2.100 | 2.100 |
| Rmerge | 0.024 | 0.368 |
| Rmeas | 0.034 | 0.520 |
| Number of reflections | 130333 | 12870 |
| <I/σ(I)> | 20.91 | 2.11 |
| Completeness [%] | 99.0 | |
| Redundancy | 1.9 | |
| CC(1/2) | 0.998 | 0.735 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 5.5 | 293 | 15% PEG3350, 0.4 M LiSO4, 0.1 M bis-tris pH 5.5 |






