7YQS
Neutron structure of a L-rhamnose-alpha-1,4-D-glucuronate lyase from Fusarium oxysporum 12S, L-Rha complex
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PHOTON FACTORY BEAMLINE BL-5A |
| Synchrotron site | Photon Factory |
| Beamline | BL-5A |
| Temperature [K] | 293 |
| Detector technology | PIXEL |
| Collection date | 2021-03-17 |
| Detector | DECTRIS PILATUS3 S 6M |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 57.780, 65.800, 108.950 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 19.820 - 1.800 |
| R-factor | 0.1634 |
| Rwork | 0.162 |
| R-free | 0.19070 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 7esk |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.160 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHENIX (1.17.1_3660) |
| Refinement software | PHENIX (1.17.1_3660) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 43.420 | 1.860 | 1.270 |
| High resolution limit [Å] | 1.250 | 1.800 | 1.250 |
| Rmerge | 0.059 | 1.174 | 0.886 |
| Rpim | 0.025 | 0.507 | 0.380 |
| Number of reflections | 115388 | 3825 | 5667 |
| <I/σ(I)> | 15 | 1.6 | 2.2 |
| Completeness [%] | 100.0 | 98 | 100 |
| Redundancy | 6.4 | 5.9 | 6.4 |
| CC(1/2) | 0.999 | 0.411 | 0.794 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 293 | Protein solution : protein 24mg/ml, 20mM Tris-DCl (pD 8.0), Reservoir solution : 33 % (w/v) PEG 1500, 0.1 M Tris-DCl (pD 8.5), 0.1 M L-Rha |
| 1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 293 | Protein solution : protein 24mg/ml, 20mM Tris-DCl (pD 8.0), Reservoir solution : 33 % (w/v) PEG 1500, 0.1 M Tris-DCl (pD 8.5), 0.1 M L-Rha |






