1OB8
Holliday Junction Resolving Enzyme
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SRS BEAMLINE PX9.6 |
| Synchrotron site | SRS |
| Beamline | PX9.6 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2002-06-04 |
| Detector | ADSC CCD |
| Spacegroup name | P 65 |
| Unit cell lengths | 90.577, 90.577, 70.920 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 24.540 - 1.800 |
| Rwork | 0.197 |
| R-free | 0.24600 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | SE-SAD DERIVED STRUCTURE |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.292 |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Refinement software | REFMAC (5.1.19) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 25.000 | 1.830 |
| High resolution limit [Å] | 1.800 | 1.800 |
| Number of reflections | 30127 | |
| <I/σ(I)> | 41.1 | 1.75 |
| Completeness [%] | 98.0 | 94.1 |
| Redundancy | 4.25 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | 9 | 293 | 0.2M LITHIUM SULFATE,0.1M TRIS PH 9 20% PEG 4000,15% ETHYLENE GLYCOL,293K |






