Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I03 |
Synchrotron site | Diamond |
Beamline | I03 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-08-04 |
Detector | DECTRIS EIGER2 X 16M |
Wavelength(s) | 0.9762 |
Spacegroup name | P 41 2 2 |
Unit cell lengths | 102.000, 102.000, 278.850 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 57.621 - 1.880 |
Rwork | 0.202 |
R-free | 0.23620 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2a39 |
RMSD bond length | 0.013 |
RMSD bond angle | 1.786 |
Data reduction software | xia2 |
Data scaling software | xia2 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 57.621 | 1.910 |
High resolution limit [Å] | 1.880 | 1.880 |
Rmeas | 0.177 | 2.978 |
Number of reflections | 120246 | 8348 |
<I/σ(I)> | 14.2 | 1.1 |
Completeness [%] | 100.0 | 100 |
Redundancy | 16.2 | 16.1 |
CC(1/2) | 1.000 | 0.500 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8 | 298 | 12 mg/mL protein in 20 mM pH 8 Tris buffer mixed 2:1 with 0.15 M sodium citrate, 0.8 M ammonium sulfate, 1 M lithium sulfate |