4BKG
crystal structure of human diSUMO-2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SEALED TUBE |
Source details | OXFORD DIFFRACTION NOVA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-01-24 |
Detector | OXFORD DIFFRACTION |
Wavelength(s) | 1.5406 |
Spacegroup name | H 3 |
Unit cell lengths | 74.988, 74.988, 33.267 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.760 - 2.110 |
R-factor | 0.18092 |
Rwork | 0.179 |
R-free | 0.23074 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1wm3 |
RMSD bond length | 0.019 |
RMSD bond angle | 1.879 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 23.240 | 2.170 |
High resolution limit [Å] | 2.100 | 2.100 |
Rmerge | 0.060 | 0.440 |
Number of reflections | 3842 | |
<I/σ(I)> | 12.5 | 1.9 |
Completeness [%] | 94.8 | 73.9 |
Redundancy | 2.8 | 1.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8 | 0.1 M TRIS/HCL PH 8.0, 28% PEG 350MME,0.05% DIOXANE |