8T2M
Crystal structure of GABARAP in complex with the LIR of NSs4
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CLSI BEAMLINE 08B1-1 |
Synchrotron site | CLSI |
Beamline | 08B1-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2021-12-15 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 1.18057 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 32.741, 59.119, 67.346 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.450 - 1.270 |
R-factor | 0.1597 |
Rwork | 0.159 |
R-free | 0.17760 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.009 |
RMSD bond angle | 0.964 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 29.450 | 1.310 |
High resolution limit [Å] | 1.270 | 1.271 |
Number of reflections | 33702 | 2064 |
<I/σ(I)> | 20.69 | |
Completeness [%] | 95.7 | |
Redundancy | 11.3 | |
CC(1/2) | 1.000 | 0.567 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 0.1 M sodium acetate:HCl, pH 4.6, 8% PEG 4000 |