5NPW
Structure of human ATG5-ATG16L1(ATG5BD) complex (C2)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06DA |
Synchrotron site | SLS |
Beamline | X06DA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-09-08 |
Detector | DECTRIS PILATUS 2M |
Wavelength(s) | 1.0000 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 200.860, 75.990, 142.440 |
Unit cell angles | 90.00, 131.41, 90.00 |
Refinement procedure
Resolution | 48.316 - 3.100 |
R-factor | 0.2198 |
Rwork | 0.217 |
R-free | 0.26390 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4gdk |
RMSD bond length | 0.003 |
RMSD bond angle | 0.504 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 48.316 | 48.316 | 3.200 |
High resolution limit [Å] | 3.100 | 10.000 | 3.100 |
Rmerge | 0.126 | 0.037 | 0.745 |
Rmeas | 0.147 | 0.043 | 0.865 |
Number of reflections | 29428 | 929 | 2643 |
<I/σ(I)> | 9.48 | 27.66 | 2.08 |
Completeness [%] | 99.1 | 96.7 | 99.3 |
Redundancy | 3.698 | 3.771 | 3.841 |
CC(1/2) | 0.992 | 0.997 | 0.687 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.4 M KCl and 18 % PEG 3350 |