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 |