5V42
Crystal Structure of Mtb Pks13 Thioesterase domain in complex with inhibitor TAM3
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] | 100 |
| Detector technology | CCD |
| Collection date | 2013-06-10 |
| Detector | MARMOSAIC 300 mm CCD |
| Wavelength(s) | 1.0032 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 89.362, 109.399, 56.895 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 33.763 - 1.987 |
| R-factor | 0.1963 |
| Rwork | 0.194 |
| R-free | 0.23330 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5v3w |
| RMSD bond length | 0.008 |
| RMSD bond angle | 1.119 |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | PHENIX |
| Refinement software | PHENIX |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 50.000 | 2.020 |
| High resolution limit [Å] | 1.987 | 5.400 | 1.990 |
| Rmerge | 0.106 | 0.042 | |
| Rmeas | 0.110 | 0.047 | |
| Rpim | 0.053 | 0.019 | 0.633 |
| Number of reflections | 34501 | ||
| <I/σ(I)> | 8.1 | ||
| Completeness [%] | 88.0 | 86.1 | 83.8 |
| Redundancy | 5.2 | 5.6 | 4.4 |
| CC(1/2) | 0.998 | 0.458 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 290 | 0.1 M Tris-HCl, 2.0-1.8 M ammonium sulfate, 2%-5% v/v PPG P400 |






