6J7I
Fusion protein of heme oxygenase-1 and NADPH cytochrome P450 reductase (15aa)
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 | 2016-12-14 |
Detector | RAYONIX MX225HE |
Wavelength(s) | 0.9 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 82.771, 158.101, 188.515 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 40.037 - 3.300 |
R-factor | 0.1952 |
Rwork | 0.192 |
R-free | 0.24060 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6j79 |
RMSD bond length | 0.003 |
RMSD bond angle | 0.727 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | PHENIX ((1.13_2998: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.360 |
High resolution limit [Å] | 3.300 | 3.300 |
Number of reflections | 35507 | 1673 |
<I/σ(I)> | 8.2 | 1.97 |
Completeness [%] | 91.6 | 88.6 |
Redundancy | 3.3 | |
CC(1/2) | 0.707 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6 | 293 | PEG 20000, MES-NaOH, ethyl acetate |