7KS8
Crystal structure of human CYP3A4 with the caged inhibitor
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL12-1 |
Synchrotron site | SSRL |
Beamline | BL12-1 |
Temperature [K] | 77 |
Detector technology | PIXEL |
Collection date | 2018-03-29 |
Detector | DECTRIS PILATUS 300K |
Wavelength(s) | 0.98 |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 76.759, 101.160, 127.440 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 40.091 - 2.500 |
R-factor | 0.2133 |
Rwork | 0.211 |
R-free | 0.26240 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5vcc |
RMSD bond length | 0.011 |
RMSD bond angle | 1.155 |
Data reduction software | iMOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((1.11.1_2575)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 79.230 | 2.640 |
High resolution limit [Å] | 2.500 | 2.500 |
Number of reflections | 16978 | 356 |
<I/σ(I)> | 7.3 | |
Completeness [%] | 97.3 | 98 |
Redundancy | 3.9 | 3.9 |
CC(1/2) | 0.996 | 0.306 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | MICROBATCH | 7 | 298 | PEG 3335, ammonium citrate |