4E28
Structure of human thymidylate synthase in inactive conformation with a novel non-peptidic inhibitor
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.3.1 |
Synchrotron site | ALS |
Beamline | 8.3.1 |
Temperature [K] | 273 |
Detector technology | CCD |
Collection date | 2009-03-20 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.11588 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 95.747, 95.747, 82.407 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 29.225 - 2.302 |
R-factor | 0.1903 |
Rwork | 0.188 |
R-free | 0.22890 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1hvy |
RMSD bond length | 0.009 |
RMSD bond angle | 1.246 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX (1.7.2_869) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 40.000 |
High resolution limit [Å] | 2.300 |
Rmerge | 0.061 |
Number of reflections | 18949 |
<I/σ(I)> | 11 |
Completeness [%] | 96.1 |
Redundancy | 3.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 273 | 1.4 M ammonium sulfate, 20 uM BME, 0.1 M Tris, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 273K |