7N10
Co-crystal structure of Prx with ComR DNA binding domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH | 
| Source type | SYNCHROTRON | 
| Source details | ALS BEAMLINE 8.3.1 | 
| Synchrotron site | ALS | 
| Beamline | 8.3.1 | 
| Temperature [K] | 100 | 
| Detector technology | PIXEL | 
| Collection date | 2020-10-21 | 
| Detector | DECTRIS PILATUS3 6M | 
| Wavelength(s) | 1.28329 | 
| Spacegroup name | P 21 21 21 | 
| Unit cell lengths | 38.556, 41.918, 90.000 | 
| Unit cell angles | 90.00, 90.00, 90.00 | 
Refinement procedure
| Resolution | 45.000 - 1.650 | 
| R-factor | 0.1763 | 
| Rwork | 0.175 | 
| R-free | 0.19710 | 
| Structure solution method | MOLECULAR REPLACEMENT | 
| Starting model (for MR) | 6cka | 
| RMSD bond length | 0.004 | 
| RMSD bond angle | 0.655 | 
| Data reduction software | XDS | 
| Data scaling software | XDS | 
| Phasing software | PHENIX | 
| Refinement software | PHENIX (1.19_4092) | 
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 45.000 | 1.680 | 
| High resolution limit [Å] | 1.650 | 1.650 | 
| Rmerge | 0.067 | 0.727 | 
| Rpim | 0.027 | 0.316 | 
| Number of reflections | 18234 | 918 | 
| <I/σ(I)> | 15.2 | 2.3 | 
| Completeness [%] | 99.9 | 100 | 
| Redundancy | 6.1 | 6.1 | 
| CC(1/2) | 0.998 | 0.867 | 
Crystallization Conditions
| crystal ID | method | pH | temperature | details | 
| 1 | VAPOR DIFFUSION, SITTING DROP | 277 | 15 mg/mL protein, 20% PEG3500, 0.2 M potassium acetate | 






