6JBM
Crystal structure of the TRIM14 PRYSPRY domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 298 |
Detector technology | PIXEL |
Collection date | 2018-09-21 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.97915 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 48.326, 104.020, 93.381 |
Unit cell angles | 90.00, 91.49, 90.00 |
Refinement procedure
Resolution | 35.396 - 2.100 |
R-factor | 0.2146 |
Rwork | 0.213 |
R-free | 0.24250 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4n7i |
RMSD bond length | 0.010 |
RMSD bond angle | 1.211 |
Data scaling software | HKL-2000 |
Refinement software | PHENIX ((1.11.1_2575: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.150 |
High resolution limit [Å] | 2.100 | 2.100 |
Number of reflections | 46284 | |
<I/σ(I)> | 9.39 | |
Completeness [%] | 99.4 | |
Redundancy | 3.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6 | 293 | Ammonium sulfate, PEG8000 |