4UF1
Deerpox virus DPV022 in complex with Bak BH3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-06-25 |
Detector | ADSC QUANTUM 315r |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 93.260, 93.260, 45.620 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.707 - 2.300 |
R-factor | 0.1796 |
Rwork | 0.178 |
R-free | 0.20590 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | DPV022_BIM |
RMSD bond length | 0.004 |
RMSD bond angle | 0.732 |
Data reduction software | iMOSFLM |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.710 | 2.390 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.100 | 0.580 |
Number of reflections | 9129 | |
<I/σ(I)> | 10.9 | 3.1 |
Completeness [%] | 97.7 | 99 |
Redundancy | 5.7 | 5.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 5.5 | 17% PEG 8000, 0.2M MES PH 5.5, 0.2M AMMONIUM SULPHATE |