2ZCV
Crystal structure of NADPH-dependent quinone oxidoreductase QOR2 complexed with NADPH from escherichia coli
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PAL/PLS BEAMLINE 6B |
| Synchrotron site | PAL/PLS |
| Beamline | 6B |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2003-05-10 |
| Detector | BRUKER PROTEUM 300 |
| Spacegroup name | P 32 2 1 |
| Unit cell lengths | 81.284, 81.284, 77.506 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 19.520 - 2.300 |
| R-factor | 0.217 |
| Rwork | 0.217 |
| R-free | 0.29800 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2zcu |
| RMSD bond length | 0.005 |
| RMSD bond angle | 1.200 |
| Data reduction software | SMART |
| Data scaling software | SAINT (& PROSCALE) |
| Phasing software | CNS |
| Refinement software | CNS |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 20.000 | 2.400 |
| High resolution limit [Å] | 2.300 | 2.300 |
| Number of reflections | 13535 | |
| Completeness [%] | 86.9 | 82 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 7.5 | 285 | PEG 4000, COPPER CHLRORIDE, HEPES, AMMONIUM SULFATE, pH 7.50, EVAPORATION, temperature 285K |






