1AOH
SINGLE COHESIN DOMAIN FROM THE SCAFFOLDING PROTEIN CIPA OF THE CLOSTRIDIUM THERMOCELLUM CELLULOSOME
Experimental procedure
Source type | SYNCHROTRON |
Source details | LURE BEAMLINE DW32 |
Synchrotron site | LURE |
Beamline | DW32 |
Temperature [K] | 110 |
Detector technology | IMAGE PLATE |
Collection date | 1996-11 |
Detector | MARRESEARCH |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 37.840, 80.500, 93.240 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 10.000 - 1.700 |
R-factor | 0.194 |
Rwork | 0.194 |
R-free | 0.26000 * |
Structure solution method | MIR |
RMSD bond length | 0.014 |
RMSD bond angle | 28.240 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | X-PLOR (3.1) |
Refinement software | X-PLOR (3.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 1.760 |
High resolution limit [Å] | 1.700 | 1.700 |
Rmerge | 0.055 | 0.253 |
Total number of observations | 175259 * | |
Number of reflections | 29669 | |
<I/σ(I)> | 22.2 | 4.5 |
Completeness [%] | 92.2 | 86.6 |
Redundancy | 5.8 | 3.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 6.25 | Beguin, P., (1996) Protein Sci., 5, 1192 * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | PEG8000 | 18 (%(w/v)) | |
2 | 1 | reservoir | calcium acetate | 0.2 (M) | |
3 | 1 | reservoir | glycerol | 6 (%(v/v)) | |
4 | 1 | reservoir | sodium cacodylate | 0.05 (M) | |
5 | 1 | drop | PEG8000 | 9 (%(w/v)) | |
6 | 1 | drop | calcium acetate | 0.1 (M) | |
7 | 1 | drop | glycerol | 3 (%(v/v)) | |
8 | 1 | drop | sodium cacodylate | 0.025 (M) | pH6.25 |
9 | 1 | drop | protein | 7.5-10 (mg/ml) |