4MVT
Crystal structure of SUMO E3 Ligase PIAS3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-08-15 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97918 |
Spacegroup name | P 1 |
Unit cell lengths | 55.450, 85.440, 89.530 |
Unit cell angles | 83.08, 86.57, 86.14 |
Refinement procedure
Resolution | 48.040 - 2.300 |
R-factor | 0.239 |
Rwork | 0.238 |
R-free | 0.26980 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4fo9 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | MOLREP (11.0) |
Refinement software | REFMAC |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 2.340 |
High resolution limit [Å] | 2.300 | 6.240 | 2.300 |
Rmerge | 0.137 | 0.080 | 0.950 |
Number of reflections | 71156 | ||
<I/σ(I)> | 18.1 | ||
Completeness [%] | 98.4 | 98.6 | 97.6 |
Redundancy | 5.1 | 4.9 | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8.5 | 291 | 20% PEG 8000, 0.2 M Magnesium Chloride, 0.1 M Tris pH8.5,(1:800-1:1300) w/w chymotrypsin, vapor diffusion hanging drop, temperature 291K |