3NV6
Crystal Structure of Camphor-Bound CYP101D2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU MICROMAX-007 |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2008-03-18 |
Detector | MAR scanner 345 mm plate |
Wavelength(s) | 1.5418 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 86.080, 86.080, 123.867 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 47.640 - 2.200 |
R-factor | 0.19187 |
Rwork | 0.189 |
R-free | 0.25458 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3nv5 |
RMSD bond length | 0.016 |
RMSD bond angle | 1.683 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0044) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.280 |
High resolution limit [Å] | 2.200 | 2.200 |
Rmerge | 0.043 | 0.232 |
Number of reflections | 27333 | |
<I/σ(I)> | 33.2 | 5.8 |
Completeness [%] | 99.0 | 99.5 |
Redundancy | 4.7 | 4.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8.3 | 291 | 0.1M Tris, pH 8.3, 2.1M ammonium sulfate, 4% PEG 400, VAPOR DIFFUSION, HANGING DROP, temperature 291K |