8FRT
X-ray crystal structure of the N-terminal region from HCMV US11 binding to HLA-A*02:01
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-09-19 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.954 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 52.386, 80.503, 56.082 |
Unit cell angles | 90.00, 113.49, 90.00 |
Refinement procedure
Resolution | 48.040 - 1.800 |
Rwork | 0.206 |
R-free | 0.23890 |
Structure solution method | MOLECULAR REPLACEMENT |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (v1.20.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.040 | 1.840 |
High resolution limit [Å] | 1.800 | 1.800 |
Number of reflections | 39611 | 2325 |
<I/σ(I)> | 6.8 | |
Completeness [%] | 100.0 | |
Redundancy | 3.5 | |
CC(1/2) | 0.996 | 0.704 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 293 | 30% (w/v) PEG3350, 0.1 M DL-malic acid pH 7.0, 83 mM cesium chloride |