5I9E
Crystal structure of a nuclear actin ternary complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-06-01 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.987 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 110.260, 202.220, 87.010 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 48.403 - 2.800 |
R-factor | 0.2338 |
Rwork | 0.232 |
R-free | 0.28440 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3qb0 1yag |
RMSD bond length | 0.007 |
RMSD bond angle | 0.708 |
Data reduction software | HKL-2000 (V705) |
Data scaling software | HKL-2000 (V705) |
Phasing software | PHASER (5) |
Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.403 | 2.870 |
High resolution limit [Å] | 2.800 | 2.800 |
Rmerge | 0.120 | |
Number of reflections | 48531 | |
<I/σ(I)> | 15.4 | |
Completeness [%] | 99.7 | |
Redundancy | 9.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 291 | polyethylene glycol (PEG) 3350, citric acid, BIS-TRIS propane |