6BE3
Crystal structure of a polysaccharide-binding human Fab (F598) in complex with N-acetyl-D-glucosamine (GlcNAc)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2016-11-17 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.9537 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 89.263, 103.772, 105.273 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 32.254 - 1.600 |
| R-factor | 0.1673 |
| Rwork | 0.166 |
| R-free | 0.19980 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6be2 |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.864 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 32.254 | 1.690 |
| High resolution limit [Å] | 1.600 | 1.600 |
| Rmerge | 0.092 | 0.382 |
| Rmeas | 0.099 | 0.412 |
| Number of reflections | 64007 | 10070 |
| <I/σ(I)> | 13.16 | |
| Completeness [%] | 98.6 | 97 |
| Redundancy | 7.1 | 7.1 |
| CC(1/2) | 0.996 | 0.949 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 291 | 15% PEG 4000, 20% iso-propanol, 0.1 M sodium citrate pH 5.6 |






