3G1E
X-ray crystal structure of coil 1A of human vimentin
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SEALED TUBE |
| Source details | OXFORD DIFFRACTION ENHANCE ULTRA |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2006-01-10 |
| Detector | OXFORD ONYX CCD |
| Spacegroup name | P 41 21 2 |
| Unit cell lengths | 35.496, 35.496, 108.022 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 11.650 - 1.830 |
| Rwork | 0.253 |
| R-free | 0.29500 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | DIMERIC MODEL BUILT FROM PDB ENTRIES 1GK7 AND 1D7M |
| RMSD bond length | 0.005 |
| RMSD bond angle | 1.200 |
| Data reduction software | CrysalisPro (PRO (OXFORD DIFFRACTION)) |
| Data scaling software | SCALA |
| Phasing software | PHASER |
| Refinement software | CNS (1.2) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 11.650 | 1.860 |
| High resolution limit [Å] | 1.770 | 1.770 |
| Rmerge | 0.099 | 0.414 |
| Number of reflections | 6364 | |
| <I/σ(I)> | 7 | 1.6 |
| Completeness [%] | 87.5 | 43.8 |
| Redundancy | 9.3 | 2.5 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | 5.6 | 298 | 20 % PEG, 33 % isopropanol, 0.1 M trisodium citrate, pH 5.6, vapour diffusion, temperature 298K |






