4MBG
Crystal structure of Aspergillus fumigatus protein farnesyltransferase binary complex with farnesyldiphosphate
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 22-BM |
| Synchrotron site | APS |
| Beamline | 22-BM |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2012-06-08 |
| Detector | MARMOSAIC 225 mm CCD |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 63.252, 90.793, 83.138 |
| Unit cell angles | 90.00, 110.87, 90.00 |
Refinement procedure
| Resolution | 23.960 - 1.740 |
| R-factor | 0.124 |
| Rwork | 0.122 |
| R-free | 0.16400 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | HOMOLOGY MODEL OF ASPERGILLUS FUMIGATUS PROTEIN FARNESYLTRANSFERASE GENERATED USING PHYRE |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.231 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASES |
| Refinement software | PHENIX ((phenix.refine: 1.8_1069)) |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 50.000 |
| High resolution limit [Å] | 1.740 |
| Number of reflections | 89198 |
| Completeness [%] | 99.8 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | 7.5 | 290 | 4-10 % PEG6000, 600-800 mM LiCl, and 100 mM HEPES pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 290K |






