8W0O
GDH-105 crystal structure
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2023-03-18 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9537 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 63.336, 120.428, 125.775 |
Unit cell angles | 90.00, 101.89, 90.00 |
Refinement procedure
Resolution | 49.000 - 1.660 |
Rwork | 0.173 |
R-free | 0.19650 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.008 |
RMSD bond angle | 1.361 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0405) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.000 | 1.690 |
High resolution limit [Å] | 1.660 | 1.660 |
Rmerge | 0.141 | 1.323 |
Rpim | 0.058 | 0.541 |
Number of reflections | 212485 | 9477 |
<I/σ(I)> | 9.3 | 1.4 |
Completeness [%] | 98.0 | 88.9 |
Redundancy | 6.9 | 6.8 |
CC(1/2) | 0.997 | 0.609 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6 | 295 | Crystals were grown in 30% PEG4000 with 200 mM malate imidazole buffer at pH 6.0. Sitting drops were 200 nL of reservoir with 200 nL of protein at about 10 mg/mL at room temperature. |