4QN1
Crystal Structure of a Functionally Uncharacterized Domain of E3 Ubiquitin Ligase SHPRH
Experimental procedure
Experimental method | SAD |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-04-11 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97918 |
Spacegroup name | P 61 2 2 |
Unit cell lengths | 130.624, 130.624, 129.571 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 27.770 - 2.480 |
R-factor | 0.2268 |
Rwork | 0.226 |
R-free | 0.25740 |
Structure solution method | SAD |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | SOLVE |
Refinement software | REFMAC |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 2.520 |
High resolution limit [Å] | 2.480 | 6.730 | 2.480 |
Rmerge | 0.117 | 0.053 | 0.951 |
Number of reflections | 23412 | ||
<I/σ(I)> | 24.3 | ||
Completeness [%] | 98.5 | 95 | 99.5 |
Redundancy | 9.5 | 8.8 | 9.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 291 | 1.6 M ammonium formate, 0.1 M Bis-Tris, pH 5.5, in situ proteolysis (1000:1 w/w protein:chymotrypsin) before setup, VAPOR DIFFUSION, HANGING DROP, temperature 291K |