5I8O
HMM5 Fab in complex with disaccharide
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID23-2 |
| Synchrotron site | ESRF |
| Beamline | ID23-2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2014-09-14 |
| Detector | DECTRIS PILATUS3 2M |
| Wavelength(s) | 0.8726 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 63.447, 63.587, 108.771 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 44.913 - 1.800 |
| R-factor | 0.1663 |
| Rwork | 0.164 |
| R-free | 0.20470 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.122 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | PHENIX |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 44.913 | 1.860 | |
| High resolution limit [Å] | 1.800 | 3.880 | 1.800 |
| Rmerge | 0.170 | 0.060 | 0.982 |
| Number of reflections | 41574 | ||
| <I/σ(I)> | 9.05 | 25.05 | 1.72 |
| Completeness [%] | 100.0 | 99.8 | 100 |
| Redundancy | 6.594 | ||
| CC(1/2) | 0.995 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 292 | 15-25 mM LiSO4, 15-26.5% (w/v) PEG 3350, 0.1M Tris or HEPES pH 7.0-8.5, 18 mM Fuca1-3GlcNAca1-OMe |






