4CG4
Crystal structure of the CHS-B30.2 domains of TRIM20
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2011-09-13 |
Detector | DECTRIS PILATUS 6M |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 69.820, 388.210, 70.880 |
Unit cell angles | 90.00, 116.52, 90.00 |
Refinement procedure
Resolution | 48.526 - 2.400 |
R-factor | 0.214 |
Rwork | 0.211 |
R-free | 0.26070 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2wl1 |
RMSD bond length | 0.012 |
RMSD bond angle | 1.378 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.530 | 2.490 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.170 | |
Number of reflections | 129351 | |
<I/σ(I)> | 9.77 | 0.88 |
Completeness [%] | 98.9 | 93.1 |
Redundancy | 7.4 | 6.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | 0.1 M TRIS-ACOH PH 7.4-8, 0.26% (W/V) CYSTAMINE-HCL, 0.2 M LISO4, 8% (W/V) PEG 20000, 8% (W/V) PEG 550 MME |