6DUJ
Crystal structure of A51V variant of Human Cytochrome c
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL9-2 |
Synchrotron site | SSRL |
Beamline | BL9-2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-03-22 |
Detector | DECTRIS PILATUS 6M-F |
Wavelength(s) | 1.07 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 62.380, 184.369, 35.740 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 33.323 - 1.822 |
R-factor | 0.189334445331 |
Rwork | 0.184 |
R-free | 0.23488 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5ty3 |
RMSD bond length | 0.017 |
RMSD bond angle | 1.248 |
Data reduction software | MOSFLM |
Data scaling software | Aimless |
Phasing software | MOLREP |
Refinement software | PHENIX (1.11.1_2575) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 33.330 | 1.890 |
High resolution limit [Å] | 1.820 | 1.830 |
Rmerge | 0.106 | 1.180 |
Number of reflections | 18770 | 1878 |
<I/σ(I)> | 24.5 | |
Completeness [%] | 98.7 | 99 |
Redundancy | 6.5 | 5.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293.15 | 0.1 M sodium citrate pH 5.5, 40%(w/v) PEG 600 |