5C6K
Bacteriophage P2 integrase catalytic domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-06-29 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.9184 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 215.004, 54.420, 38.610 |
Unit cell angles | 90.00, 97.33, 90.00 |
Refinement procedure
Resolution | 35.541 - 1.900 |
R-factor | 0.1729 |
Rwork | 0.171 |
R-free | 0.20090 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1aih |
RMSD bond length | 0.007 |
RMSD bond angle | 1.011 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 38.290 | 1.940 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.084 | |
Number of reflections | 34250 | |
<I/σ(I)> | 11.6 | 2.4 |
Completeness [%] | 97.9 | 96.2 |
Redundancy | 4.1 | 4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293 | 0.2 M Sodium nitrate, 0.1 M BisTris propane pH7.5, 20 % (w/v) PEG 3350 |