7XZ1
TRIM E3 ubiquitin ligase
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PAL/PLS BEAMLINE 5C (4A) |
| Synchrotron site | PAL/PLS |
| Beamline | 5C (4A) |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2013-07-26 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 1.00933 |
| Spacegroup name | I 41 2 2 |
| Unit cell lengths | 235.921, 235.921, 158.814 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 38.860 - 5.200 |
| R-factor | 0.2709 |
| Rwork | 0.266 |
| R-free | 0.31520 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 7xv2 |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.691 |
| 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 | 5.290 |
| High resolution limit [Å] | 5.200 | 5.200 |
| Rmerge | 0.135 | |
| Number of reflections | 9007 | 452 |
| <I/σ(I)> | 49.84 | |
| Completeness [%] | 99.9 | |
| Redundancy | 28.8 | |
| CC(1/2) | 0.992 | 0.523 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 277 | 100 mM Hepes-NaOH pH 7.5, 250 mM MgCl2, 37% (w/v) 5/4 PO/OH |






