9DR8
Crystal structure of Catechol 1,2-dioxygenase from Burkholderia multivorans (Iron bound)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS-II BEAMLINE 19-ID |
Synchrotron site | NSLS-II |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2024-07-14 |
Detector | DECTRIS EIGER2 XE 9M |
Wavelength(s) | 0.9786 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 115.467, 52.327, 120.396 |
Unit cell angles | 90.00, 92.50, 90.00 |
Refinement procedure
Resolution | 57.680 - 1.420 |
R-factor | 0.145 |
Rwork | 0.143 |
R-free | 0.17270 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.005 |
RMSD bond angle | 0.807 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX ((dev_5449: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 120.280 | 1.460 |
High resolution limit [Å] | 1.420 | 1.420 |
Rmerge | 0.090 | 1.143 |
Rmeas | 0.098 | 1.240 |
Rpim | 0.039 | 0.475 |
Total number of observations | 874961 | 66205 |
Number of reflections | 135545 | 10027 |
<I/σ(I)> | 9.8 | 1.6 |
Completeness [%] | 99.9 | |
Redundancy | 6.5 | 6.6 |
CC(1/2) | 0.998 | 0.786 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 291 | 25% (w/v) 4000, 0.2M CaCl2, 0.1M Tris 8.5, BumuA.00107.d.A2.PW32075 at 21.7 mg/mL. plate Liu-S-128 B7. Protein prepared in the presence of FeCl2. Puck: PSL-1602, Cryo: 32% (w/v) 4000, 0.2M CaCl2, 0.1M Tris 8.5 |