6L9I
Crystal Structure of Lactobacillus farciminis Oxalate Decarboxylase Formate Complex
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL17U |
| Synchrotron site | SSRF |
| Beamline | BL17U |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2018-12-01 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.987 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 92.957, 122.842, 115.223 |
| Unit cell angles | 90.00, 92.47, 90.00 |
Refinement procedure
| Resolution | 48.000 - 2.790 |
| R-factor | 0.1986 |
| Rwork | 0.197 |
| R-free | 0.22940 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1uw8 |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.109 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.17_3644) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.920 |
| High resolution limit [Å] | 2.790 | 2.790 |
| Rmeas | 0.751 | |
| Number of reflections | 62238 | 5989 |
| <I/σ(I)> | 8.25 | 2.857 |
| Completeness [%] | 98.8 | |
| Redundancy | 6.3 | |
| CC(1/2) | 0.952 | 0.810 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 5.5 | 298 | 18% PEG 3350, 0.2M NH4Cl, 0.2M Sodium dihydrogen phosphate, 0.2M Bis-Tris pH5.5 |






