9JQW
The Crystal Structure of LCC6-Active from Biortus
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL10U2 |
Synchrotron site | SSRF |
Beamline | BL10U2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2024-05-11 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.979191 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 39.611, 74.690, 157.453 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.979 - 2.050 |
Rwork | 0.150 |
R-free | 0.20180 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 7vve |
RMSD bond length | 0.007 |
RMSD bond angle | 1.336 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0352) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.980 | 2.110 |
High resolution limit [Å] | 2.050 | 2.050 |
Rmerge | 0.194 | 0.979 |
Number of reflections | 30250 | 2289 |
<I/σ(I)> | 10.5 | |
Completeness [%] | 99.9 | |
Redundancy | 10 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.2M (NH4)2SO4, 0.1M Mes pH6.5, 30% w/v Polyethylene glycol Monomethyl ether 5,000 |