5DCN
Crystal structure of LC3 in complex with TECPR2 LIR
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SLS BEAMLINE X06DA |
| Synchrotron site | SLS |
| Beamline | X06DA |
| Temperature [K] | 80 |
| Detector technology | PIXEL |
| Collection date | 2015-05-09 |
| Detector | PSI PILATUS 6M |
| Wavelength(s) | 0.99987 |
| Spacegroup name | P 32 2 1 |
| Unit cell lengths | 60.705, 60.705, 99.946 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 19.489 - 2.000 |
| R-factor | 0.2131 |
| Rwork | 0.209 |
| R-free | 0.24730 |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.648 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | MOLREP |
| Refinement software | PHENIX |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 19.870 |
| High resolution limit [Å] | 2.000 |
| Number of reflections | 14950 |
| <I/σ(I)> | 24.2 |
| Completeness [%] | 99.8 |
| Redundancy | 19.4 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | 1.8M Lithium sulphate, 0.01M Magnesium chloride, 0.05M MES monohydrate, pH5.6 |






