Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 5.0.1 |
Synchrotron site | ALS |
Beamline | 5.0.1 |
Detector technology | CCD |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 1.0322 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 45.948, 94.100, 78.508 |
Unit cell angles | 90.00, 100.36, 90.00 |
Refinement procedure
Resolution | 40.200 * - 1.900 |
R-factor | 0.20268 |
Rwork | 0.201 |
R-free | 0.24000 * |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1K8W protein component |
RMSD bond length | 0.007 |
RMSD bond angle | 0.970 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | AMoRE |
Refinement software | REFMAC (5.1.24) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 * | 1.970 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.046 | 0.340 |
Total number of observations | 184403 * | |
Number of reflections | 51411 | |
<I/σ(I)> | 12.4 | 2 |
Completeness [%] | 99.5 * | 99.5 * |
Redundancy | 3.6 | 3.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, sitting drop * | 8 * | 298 | AMMONIUM SULFATE, TRIS BUFFER, PEG3350, pH 7.5, temperature 298K, microseeding |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | Tris | 20 (mM) | pH8. |
2 | 1 | drop | 0.3 (M) | ||
3 | 1 | drop | protein | 20 (mg/ml) | |
4 | 1 | reservoir | ammonium sulfate | 0.2 (M) | |
5 | 1 | reservoir | Tris | 0.1 (M) | pH8.5 |
6 | 1 | reservoir | PEG3350 | 25 (%(w/v)) |