2ZIS
Crystal Structure of rat protein farnesyltransferase complexed with a bezoruran inhibitor and FPP
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PHOTON FACTORY BEAMLINE BL-6B |
| Synchrotron site | Photon Factory |
| Beamline | BL-6B |
| Temperature [K] | 100 |
| Detector technology | DIFFRACTOMETER |
| Collection date | 2001-06-05 |
| Detector | WEISSENBERG |
| Wavelength(s) | 1.000 |
| Spacegroup name | P 61 |
| Unit cell lengths | 171.826, 171.826, 69.063 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 42.960 - 2.600 |
| Rwork | 0.184 |
| R-free | 0.22200 |
| Structure solution method | MR |
| Starting model (for MR) | 1fpp |
| RMSD bond length | 0.006 |
| RMSD bond angle | 1.358 |
| Data reduction software | DENZO (1.9.0) |
| Data scaling software | SCALEPACK (1.9.0) |
| Phasing software | MOLREP (6.2.5) |
| Refinement software | CNX (2000) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 100.000 | 100.000 | 2.690 |
| High resolution limit [Å] | 2.600 | 5.600 | 2.600 |
| Rmerge | 0.069 | 0.023 | 0.423 |
| Number of reflections | 35232 | ||
| <I/σ(I)> | 16.1 | ||
| Completeness [%] | 97.6 | 97.3 | 93 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 4.5 | 277 | 20mg/ml protein, 0.5mM FPP, 1mM inhibitor, 10% PEG6000, 0.2M Mg acetate, 0.1M Na acetate buffer, pH4.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K |






