6BQH
Crystal structure of 5-HT2C in complex with ritanserin
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL41XU |
Synchrotron site | SPring-8 |
Beamline | BL41XU |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2016-11-08 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.000 |
Spacegroup name | C 2 2 2 |
Unit cell lengths | 88.310, 97.050, 150.230 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 48.525 - 2.700 |
R-factor | 0.2542 |
Rwork | 0.253 |
R-free | 0.27450 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4ib4 |
RMSD bond length | 0.003 |
RMSD bond angle | 0.600 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((dev_2289: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.800 |
High resolution limit [Å] | 2.700 | 2.700 |
Rmerge | 0.080 | |
Number of reflections | 17076 | 1578 |
<I/σ(I)> | 14.3 | |
Completeness [%] | 94.2 | 90.2 |
Redundancy | 10.5 | 5.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | LIPIDIC CUBIC PHASE | 293 | 0.1 M sodium citrate pH 6.0, 100mM (NH4)2SO4, 30% PEG400 |