6IJX
Crystal Structure of AKR1C1 complexed with meclofenamic acid
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SEALED TUBE |
Source details | OXFORD DIFFRACTION ENHANCE ULTRA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-07-22 |
Detector | OXFORD ONYX CCD |
Wavelength(s) | 1.5418 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 39.125, 83.262, 48.914 |
Unit cell angles | 90.00, 90.05, 90.00 |
Refinement procedure
Resolution | 24.460 - 2.200 |
R-factor | 0.1618 |
Rwork | 0.159 |
R-free | 0.21400 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3nty |
RMSD bond length | 0.009 |
RMSD bond angle | 0.966 |
Data reduction software | CrysalisPro |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX ((dev_3283: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 24.460 | 2.279 |
High resolution limit [Å] | 2.200 | 2.200 |
Rmerge | 0.090 | 0.330 |
Number of reflections | 15939 | 1580 |
<I/σ(I)> | 19.92 | |
Completeness [%] | 99.7 | |
Redundancy | 1.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | 23-27% (w/v) PEG 4000, 100 mM Hepes, 10mM CaCl2, 0.4M NaCl |