9FD5
flavin reductase ThdF in complex with two bound FADs in space group P21
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PETRA III, EMBL c/o DESY BEAMLINE P14 (MX2) |
Synchrotron site | PETRA III, EMBL c/o DESY |
Beamline | P14 (MX2) |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2022-12-10 |
Detector | DECTRIS EIGER2 X CdTe 16M |
Wavelength(s) | 0.9763 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 59.150, 77.370, 75.490 |
Unit cell angles | 90.00, 111.83, 90.00 |
Refinement procedure
Resolution | 54.070 - 1.310 |
R-factor | 0.117 |
Rwork | 0.115 |
R-free | 0.15290 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.011 |
RMSD bond angle | 1.269 |
Data reduction software | XDS (BUILT=20220220) |
Data scaling software | STARANISO (server release v3.351 25-Oct-2023) |
Phasing software | PHASER (2.8.3) |
Refinement software | PHENIX (1.21_5207) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 70.070 | 1.370 |
High resolution limit [Å] | 1.310 | 1.310 |
Rmerge | 0.057 | 0.645 |
Rmeas | 0.062 | 0.709 |
Rpim | 0.023 | 0.287 |
Number of reflections | 129944 | 6497 |
<I/σ(I)> | 16.3 | 2.5 |
Completeness [%] | 86.9 | 35.6 |
Redundancy | 6.9 | 5.7 |
CC(1/2) | 0.999 | 0.804 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 293 | B11 Proplex (Molecular Dimensions); 0.1 M HEPES pH 7.0, 15 % (w/v) PEG 4000; 18 mg/mL ThdF (50 mM HEPES pH 7.0, 20 mM NaCl, 1 mM DTT), 1:1800 (mass ratio) elastase added; 300 nL protein + 300 nL reservoir |