2F92
Crystal structure of human FPPS in complex with alendronate
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-09-05 |
Detector | MARRESEARCH |
Wavelength(s) | 1.00003 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 111.503, 111.503, 70.222 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 40.660 - 2.150 |
R-factor | 0.249 |
Rwork | 0.247 |
R-free | 0.28900 |
Structure solution method | FOURIER SYNTHESIS |
RMSD bond length | 0.007 |
RMSD bond angle | 1.000 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | CNX (2005) |
Refinement software | CNX (2005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 79.000 | 2.210 |
High resolution limit [Å] | 2.150 | 2.150 |
Rmerge | 0.068 | 0.466 |
Number of reflections | 24529 | 1791 |
<I/σ(I)> | 15.8 | 4.47 |
Completeness [%] | 99.5 | 99.7 |
Redundancy | 7.1 | 6.64 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 4.4 | 292 | 0.1M zinc acetate, 0.1M sodium acetate, 12% PEG 4000, pH 4.4, VAPOR DIFFUSION, SITTING DROP, temperature 292K |