5GN8
Structure of a 48-mer protein nanocage fabricated from its 24-mer analogue by subunit interface redesign
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-10-26 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.9789 |
Spacegroup name | F 4 3 2 |
Unit cell lengths | 236.120, 236.120, 236.120 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.741 - 2.805 |
R-factor | 0.2153 |
Rwork | 0.213 |
R-free | 0.25120 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1fha |
RMSD bond length | 0.010 |
RMSD bond angle | 0.895 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHENIX |
Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 50.000 |
High resolution limit [Å] | 2.800 |
Number of reflections | 13673 |
<I/σ(I)> | 19.1 |
Completeness [%] | 99.9 |
Redundancy | 1.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 300 | 0.1 M imidazol-HCl at pH 7.5, 10% reagent alcohol (15%) and 0.2 M MgCl2 |