6YDE
X-ray structure of LPMO
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE MASSIF-3 |
| Synchrotron site | ESRF |
| Beamline | MASSIF-3 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-04-27 |
| Detector | DECTRIS EIGER X 4M |
| Wavelength(s) | 0.90 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 39.550, 124.370, 51.670 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 50.000 - 2.200 |
| R-factor | 0.19751 |
| Rwork | 0.194 |
| R-free | 0.26356 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5ach |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | MOLREP |
| Refinement software | REFMAC (v5.8.0230) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.260 |
| High resolution limit [Å] | 2.200 | 2.200 |
| Number of reflections | 13174 | 977 |
| <I/σ(I)> | 5.03 | |
| Completeness [%] | 96.9 | |
| Redundancy | 5.41 | |
| CC(1/2) | 0.982 | 0.620 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 289.15 | 0.1 M NaCl, 0.1 M Bis-Tris pH 6.5, 1.4 M (NH4)2SO4 |






