3FNH
Crystal structure of InhA bound to triclosan derivative
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 23-ID-B |
Synchrotron site | APS |
Beamline | 23-ID-B |
Temperature [K] | 121 |
Detector technology | CCD |
Collection date | 2006-04-02 |
Detector | ADSC QUANTUM 315 |
Spacegroup name | I 41 2 2 |
Unit cell lengths | 90.022, 90.022, 183.144 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.850 - 2.800 |
R-factor | 0.2234 |
Rwork | 0.221 |
R-free | 0.26820 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1eny |
RMSD bond length | 0.020 |
RMSD bond angle | 2.245 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.910 |
High resolution limit [Å] | 2.800 | 2.800 |
Rmerge | 0.086 | 0.823 |
Number of reflections | 9708 | |
<I/σ(I)> | 22.3 | 3.7 |
Completeness [%] | 99.8 | 100 |
Redundancy | 8.5 | 8.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 293 | 0.1 M Hepes pH 7.5, 12% MPD, and 4% DMSO, VAPOR DIFFUSION, HANGING DROP, temperature 293K |