1CU1
CRYSTAL STRUCTURE OF AN ENZYME COMPLEX FROM HEPATITIS C VIRUS
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS |
Synchrotron site | APS |
Detector technology | CCD |
Detector | MARRESEARCH |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 91.360, 110.510, 141.200 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 40.000 - 2.500 |
R-factor | 0.2 |
Rwork | 0.200 |
R-free | 0.26000 |
RMSD bond length | 0.013 |
RMSD bond angle | 1.670 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | X-PLOR |
Refinement software | X-PLOR (98.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.000 | 2.590 |
High resolution limit [Å] | 2.500 | 2.500 |
Rmerge | 0.082 | 0.340 |
Total number of observations | 601477 * | |
Number of reflections | 50441 | |
<I/σ(I)> | 21 | |
Completeness [%] | 100.0 | 100 |
Redundancy | 5.6 | 5.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Batch method * | 6.4 * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | 1 | protein | 0.07 (mM) | |
2 | 1 | 1 | sodium phosphate | 0.08 (M) | |
3 | 1 | 1 | PEG6000 | 16 (%(w/v)) | |
4 | 1 | 1 | di-potassium hydrogen phosphate | 32 (mM) | |
5 | 1 | 1 | MPD | 8 (%(w/v)) | |
6 | 1 | 1 | HEPES | 5 (mM) | |
7 | 1 | 1 | 0.2 (M) | ||
8 | 1 | 1 | glycerol | 2 (%(v/v)) | |
9 | 1 | 1 | beta-mercaptoethanol | 2 (mM) |