6T5Z
Crystal structure of an AA10 LPMO from Photorhabdus luminescens
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID29 |
| Synchrotron site | ESRF |
| Beamline | ID29 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-03-30 |
| Detector | DECTRIS PILATUS 6M-F |
| Wavelength(s) | 0.976 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 76.530, 80.390, 90.910 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 58.547 - 1.600 |
| R-factor | 0.189634216194 |
| Rwork | 0.188 |
| R-free | 0.21807 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2bem |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.881 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 58.550 | 1.657 |
| High resolution limit [Å] | 1.600 | 1.600 |
| Rmerge | 0.078 | 0.547 |
| Number of reflections | 72679 | 7343 |
| <I/σ(I)> | 9.5 | 2.1 |
| Completeness [%] | 95.2 | 99.7 |
| Redundancy | 3.6 | 3.6 |
| CC(1/2) | 1.000 | 0.800 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 5.6 | 294 | precipitant: 0.1 M sodium acetate (pH 5.2), 0.7 M 1,6-hexanediol protein solution: holo-PlAA10 (10 mg/mL) in 50 mM MES (pH 6.5), 0.5 mM CuSO4 |






