6LGK
Crystal structure of an oxido-reductase with mutation
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 95 |
Detector technology | CCD |
Collection date | 2019-03-23 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.979 |
Spacegroup name | P 2 21 21 |
Unit cell lengths | 75.360, 137.170, 141.640 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 43.512 - 2.000 |
R-factor | 0.1465 |
Rwork | 0.146 |
R-free | 0.17170 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4wnc |
RMSD bond length | 0.009 |
RMSD bond angle | 0.997 |
Data reduction software | iMOSFLM |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.000 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.131 | |
Number of reflections | 99646 | 9845 |
<I/σ(I)> | 14.4 | |
Completeness [%] | 99.9 | |
Redundancy | 12 | |
CC(1/2) | 0.996 | 0.967 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 277 | 0.1M Tris, pH8.5, 25% PEG 3350 |