2Z83
Crystal Structure of Catalytic Domain of Japanese Encephalitis Virus NS3 Helicase/Nucleoside Triphosphatase at a Resolution 1.8
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL44XU |
Synchrotron site | SPring-8 |
Beamline | BL44XU |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-10-26 |
Detector | Bruker DIP-6040 |
Wavelength(s) | 0.9 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 59.062, 68.024, 65.219 |
Unit cell angles | 90.00, 116.87, 90.00 |
Refinement procedure
Resolution | 32.410 - 1.800 |
R-factor | 0.20196 |
Rwork | 0.199 |
R-free | 0.24918 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2bhr |
RMSD bond length | 0.016 |
RMSD bond angle | 1.592 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 32.410 |
High resolution limit [Å] | 1.800 |
Number of reflections | 40575 |
Completeness [%] | 99.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 293 | 15 % ethanol, 100mM Tris-HCl pH 7.0, 4% pentaerythritol etoxylate (3/4 EO/OH), VAPOR DIFFUSION, HANGING DROP, temperature 293K |