7FAU
Structure Determination of the NB1B11-RBD Complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 97.15 |
Detector technology | PIXEL |
Collection date | 2021-01-05 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.978 |
Spacegroup name | P 21 2 21 |
Unit cell lengths | 62.512, 88.835, 190.112 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 47.530 - 2.080 |
R-factor | 0.1999 |
Rwork | 0.198 |
R-free | 0.22820 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 7ch5 |
RMSD bond length | 0.006 |
RMSD bond angle | 0.871 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHENIX |
Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.130 |
High resolution limit [Å] | 2.080 | 2.080 |
Number of reflections | 64558 | 44904 |
<I/σ(I)> | 15 | |
Completeness [%] | 100.0 | |
Redundancy | 9.9 | |
CC(1/2) | 0.999 | 0.578 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293.15 | 16% PEG3350 and 0.1 M Zinc acetate, dehydrate |