8HAR
SAH-bound C-Methyltransferase Fur6 from Streptomyces sp. KO-3988
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL32XU |
Synchrotron site | SPring-8 |
Beamline | BL32XU |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-07-21 |
Detector | DECTRIS EIGER X 9M |
Wavelength(s) | 1.000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 74.980, 91.840, 125.350 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 48.134 - 2.120 |
Rwork | 0.211 |
R-free | 0.25610 |
Structure solution method | SAD |
RMSD bond length | 0.004 |
RMSD bond angle | 1.300 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | CRANK2 |
Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.180 |
High resolution limit [Å] | 2.120 | 2.120 |
Number of reflections | 94785 | 6960 |
<I/σ(I)> | 5.93 | |
Completeness [%] | 100.0 | |
Redundancy | 8.1 | |
CC(1/2) | 0.984 | 0.813 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 293 | PEG3350, calcium hydroxide, HEPES-NaOH |