6JKJ
Crystal structure of human SPSB2 in the apo-state
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-06-22 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9792 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 32.450, 75.100, 79.200 |
Unit cell angles | 90.00, 101.38, 90.00 |
Refinement procedure
Resolution | 34.490 - 1.900 |
R-factor | 0.21935 |
Rwork | 0.217 |
R-free | 0.26986 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3emw |
RMSD bond length | 0.009 |
RMSD bond angle | 1.555 |
Data reduction software | xia2 |
Data scaling software | Aimless |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0238) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 34.490 | 1.950 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.154 | 0.668 |
Number of reflections | 28566 | 2029 |
<I/σ(I)> | 7.6 | |
Completeness [%] | 97.3 | |
Redundancy | 3.4 | 3.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | 0.2M Ammonium acetate, 0.1M BIS-TRIS pH 5.5, 25% w/v Polyethylene glycol 3350 |