4DHI
Structure of C. elegans OTUB1 bound to human UBC13
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 23-ID-D |
Synchrotron site | APS |
Beamline | 23-ID-D |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-11-07 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 1.034 |
Spacegroup name | P 61 2 2 |
Unit cell lengths | 111.070, 111.070, 179.612 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 40.720 - 1.800 |
R-factor | 0.18782 |
Rwork | 0.187 |
R-free | 0.20866 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB ENTRIES 1J7D and 2ZFY |
RMSD bond length | 0.012 |
RMSD bond angle | 1.249 |
Data reduction software | iMOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0109) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 41.000 |
High resolution limit [Å] | 1.800 |
Number of reflections | 61151 |
Completeness [%] | 99.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 293 | 100 mM sodium cacodylate, 1 M trisodium citrate, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K |