6FPW
Structure of fully reduced Hydrogenase (Hyd-1)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I24 |
Synchrotron site | Diamond |
Beamline | I24 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-05-13 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.9686 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 93.835, 97.729, 182.911 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 91.460 - 1.350 |
R-factor | 0.116 |
Rwork | 0.114 |
R-free | 0.14400 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5lmm |
RMSD bond length | 0.015 |
RMSD bond angle | 1.661 |
Data reduction software | DIALS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0189) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 97.700 | 1.370 |
High resolution limit [Å] | 1.350 | 1.350 |
Rmerge | 0.113 | 1.160 |
Number of reflections | 366570 | |
<I/σ(I)> | 7.8 | 1.3 |
Completeness [%] | 100.0 | 100 |
Redundancy | 7 | 6.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5.7 | 296 | 100 mM bis-tris pH 5.7 200 mM LiSO4 150 mM NaCl 19-22% PEG 3350 |