9ULE
Crystal structure of CYP105A1 R84A complexed with diclofenac (DIF) at room temperature
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SPRING-8 BEAMLINE BL26B1 |
| Synchrotron site | SPring-8 |
| Beamline | BL26B1 |
| Temperature [K] | 293 |
| Detector technology | PIXEL |
| Collection date | 2021-05-15 |
| Detector | DECTRIS EIGER R 4M |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 53.859, 54.039, 144.700 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 36.170 - 1.860 |
| R-factor | 0.1619 |
| Rwork | 0.160 |
| R-free | 0.20760 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.007 |
| RMSD bond angle | 0.924 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | MOLREP |
| Refinement software | PHENIX (1.21.2_5419) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 1.970 |
| High resolution limit [Å] | 1.860 | 1.860 |
| Rmerge | 0.056 | 0.518 |
| Rmeas | 0.063 | 0.573 |
| Number of reflections | 35228 | 5519 |
| <I/σ(I)> | 18.81 | 3.81 |
| Completeness [%] | 96.3 | |
| Redundancy | 5.16 | |
| CC(1/2) | 0.999 | 0.884 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6.1 | 297 | 12-18% PEG4000, 10% MPD, 0.2 M NaCl and 0.1 M Bis-Tris buffer with protein concentration of 5 mg/ml. The crystal was soaked 3 times each for 10 min in the mother liquare containg 10 mM Diclofenac. The soaked crystal was placed into a glass capillary and sealed with dental wax after the solution was added to one end of the capillary. |






