6L69
Crystal structure of CYP154C2 from Streptomyces avermitilis
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 298 |
Detector technology | CCD |
Collection date | 2019-03-16 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 67.780, 53.390, 98.581 |
Unit cell angles | 90.00, 90.04, 90.00 |
Refinement procedure
Resolution | 33.890 - 1.500 |
R-factor | 0.1691 |
Rwork | 0.168 |
R-free | 0.19280 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1gwi |
RMSD bond length | 0.006 |
RMSD bond angle | 0.988 |
Data reduction software | iMOSFLM |
Data scaling software | SCALA |
Phasing software | PHENIX |
Refinement software | PHENIX (1.15.2_3472) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.580 |
High resolution limit [Å] | 1.500 | 1.500 |
Rmerge | 0.091 | 0.616 |
Number of reflections | 112411 | 16190 |
<I/σ(I)> | 13.2 | 3.2 |
Completeness [%] | 99.5 | |
Redundancy | 6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.1 M Bis-Tris (pH 6.5), 28% PEGMME 2000 |