1K9J
Complex of DC-SIGNR and GlcNAc2Man3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X26C |
Synchrotron site | NSLS |
Beamline | X26C |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2001-07-21 |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 1.1 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 50.226, 57.039, 89.263 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 43.770 - 1.900 |
R-factor | 0.194 * |
Rwork | 0.194 |
R-free | 0.24000 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.005 |
RMSD bond angle | 1.200 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | AMoRE |
Refinement software | CNS (1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.970 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.072 | 0.131 * |
Total number of observations | 843434 * | |
Number of reflections | 19033 | |
Completeness [%] | 92.0 | 83.6 * |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 21 * | Reservoir solution: 20% PEG 8000, 0.1M Hepes. Protein solution containing: 1mM CaCl2, 5mM oligosaccharide (Dextra M592)., pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 294K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 10 (mg/ml) | |
2 | 1 | drop | 1 (mM) | ||
3 | 1 | drop | GlcNAc-terminated pentasaccharide | 5 (mM) | |
4 | 1 | reservoir | PEG8000 | 20 (%) | |
5 | 1 | reservoir | HEPES | 0.1 (M) | pH7.5 |