7LK3
Crystal structure of untwinned human GABARAPL2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-06-25 |
Detector | DECTRIS EIGER X 9M |
Wavelength(s) | 0.9537 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 28.402, 58.700, 67.997 |
Unit cell angles | 90.00, 98.27, 90.00 |
Refinement procedure
Resolution | 33.650 - 1.900 |
Rwork | 0.196 |
R-free | 0.23260 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4co7 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 33.650 | 1.968 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.929 | 0.918 |
Rmeas | 0.988 | |
Number of reflections | 17461 | 1693 |
<I/σ(I)> | 14.55 | 2 |
Completeness [%] | 99.6 | 99.94 |
Redundancy | 7 | 7.2 |
CC(1/2) | 0.999 | 0.806 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 294 | 0.15 M KBr, 30% (w/v) PEG monomethyl ether 2000 |