6J94
Crystal structure of CYP97A3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-04-02 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.979 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 164.006, 70.414, 133.168 |
Unit cell angles | 90.00, 124.62, 90.00 |
Refinement procedure
Resolution | 41.963 - 2.401 |
R-factor | 0.1846 |
Rwork | 0.183 |
R-free | 0.21330 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4kf2 |
RMSD bond length | 0.005 |
RMSD bond angle | 0.947 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX (1.8.1_1168) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.490 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.090 | 0.695 |
Rmeas | 0.105 | 0.807 |
Rpim | 0.054 | 0.409 |
Number of reflections | 48368 | 4769 |
<I/σ(I)> | 15 | 2 |
Completeness [%] | 98.5 | 97.8 |
Redundancy | 3.8 | 3.9 |
CC(1/2) | 0.937 | 0.752 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | LIQUID DIFFUSION | 6.5 | 289 | 0.1 M MES, 12% (w/v) PEG 20000 |