8UY1
Methylenetetrahydrofolate reductase from Chaetomium thermophilum DSM 1495, Active (R) State
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 21-ID-D |
| Synchrotron site | APS |
| Beamline | 21-ID-D |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2022-06-30 |
| Detector | DECTRIS EIGER X 9M |
| Wavelength(s) | 1.1271 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 117.972, 151.380, 188.048 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 52.040 - 3.490 |
| R-factor | 0.21759 |
| Rwork | 0.216 |
| R-free | 0.25564 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.839 |
| Data reduction software | DIALS |
| Data scaling software | Aimless |
| Phasing software | MrBUMP |
| Refinement software | REFMAC (5.8.0419) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 52.040 | 3.530 |
| High resolution limit [Å] | 3.410 | 3.410 |
| Rmerge | 0.164 | 2.805 |
| Rmeas | 0.177 | 3.024 |
| Rpim | 0.067 | 1.122 |
| Total number of observations | 32082 | |
| Number of reflections | 46407 | 4499 |
| <I/σ(I)> | 7.7 | 0.9 |
| Completeness [%] | 99.5 | |
| Redundancy | 6.9 | 7.1 |
| CC(1/2) | 0.996 | 0.466 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293.15 | 1-1 ratio protein to reservoir solution Protein: 25 mM Tris, pH 7.4, 50 mM potassium chloride, 500 uM FAD, and 1 mM TCEP Reservoir Solution: 0.1 M HEPES, pH 7.5, 0.1 mM potassium chloride, 20 mM magnesium chloride, 22% poly(acrylic acid sodium salt) 5,100 |






