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 |






