1HQL
The xenograft antigen in complex with the B4 isolectin of Griffonia simplicifolia lectin-1
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | ROTATING ANODE |
| Source details | RIGAKU RU200 |
| Temperature [K] | 100 |
| Detector technology | IMAGE PLATE |
| Collection date | 1999-10-25 |
| Detector | RIGAKU RAXIS IV |
| Wavelength(s) | 1.5418 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 111.210, 51.280, 77.110 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 19.930 - 2.200 |
| R-factor | 0.233 * |
| Rwork | 0.233 |
| R-free | 0.25400 |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.200 |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | CNS |
| Refinement software | CNS |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 20.000 | 2.300 |
| High resolution limit [Å] | 2.200 | 2.200 |
| Rmerge | 0.142 | 0.416 |
| Number of reflections | 22043 | |
| <I/σ(I)> | 16 | 4.6 |
| Completeness [%] | 96.7 | 83.8 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 293 | Tempel, W., (2001) Acta Crystallogr., D57, 1639. * |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 293 | Tempel, W., (2001) Acta Crystallogr., D57, 1639. * |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | drop | protein | 10 (mg/ml) | |
| 2 | 1 | drop | detergent NP-40 | 0.02 (%(w/v)) | |
| 3 | 1 | reservoir | PEG4000 | 11 (%(w/v)) | |
| 4 | 1 | reservoir | MPD | 8 (%(v/v)) | |
| 5 | 1 | reservoir | DMSO | 6 (%(v/v)) | |
| 6 | 1 | reservoir | HEPES | 0.1 (M) | pH7.5 |






