7XZ0
TRIM E3 ubiquitin ligase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE AR-NE3A |
Synchrotron site | Photon Factory |
Beamline | AR-NE3A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-05-30 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 239.728, 72.967, 83.764 |
Unit cell angles | 90.00, 97.60, 90.00 |
Refinement procedure
Resolution | 37.740 - 3.280 |
R-factor | 0.2588 |
Rwork | 0.254 |
R-free | 0.30780 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 7xv2 |
RMSD bond length | 0.003 |
RMSD bond angle | 0.650 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.340 |
High resolution limit [Å] | 3.280 | 3.280 |
Number of reflections | 22376 | 1110 |
<I/σ(I)> | 21.5 | |
Completeness [%] | 98.8 | |
Redundancy | 3.9 | |
CC(1/2) | 0.995 | 0.558 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 277 | 100 mM TRIS-HCl pH 8.5, 8% (v/v) PEG 8000 |