3S4M
Crystal structure of wild-type human frataxin
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL7-1 |
Synchrotron site | SSRL |
Beamline | BL7-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-08-01 |
Detector | ADSC QUANTUM 315r |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 42.924, 44.792, 69.036 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 37.580 - 1.300 |
R-factor | 0.15506 |
Rwork | 0.153 |
R-free | 0.18738 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1ekg |
RMSD bond length | 0.031 |
RMSD bond angle | 2.725 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER (2.1) |
Refinement software | REFMAC (5.5.0102) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 44.860 | 1.370 |
High resolution limit [Å] | 1.300 | 1.300 |
Number of reflections | 33576 | |
<I/σ(I)> | 14 | 2.6 |
Completeness [%] | 100.0 | 100 |
Redundancy | 7.7 | 7.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.6 | 295 | 30% MPD, 0.1 M sodium citrate, 0.2 M ammonium acetate, pH 5.6, VAPOR DIFFUSION, HANGING DROP, temperature 295K |