7YYK
Crystal structure of the O-fucosylated form of TSRs1-3 from the human thrombospondin 1
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I03 |
| Synchrotron site | Diamond |
| Beamline | I03 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2014-05-22 |
| Detector | DECTRIS PILATUS3 S 6M |
| Wavelength(s) | 0.9762 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 66.153, 85.197, 62.121 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 20.000 - 2.600 |
| R-factor | 0.25103 |
| Rwork | 0.249 |
| R-free | 0.31663 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1lsl |
| RMSD bond length | 0.013 |
| RMSD bond angle | 1.738 |
| Data reduction software | XDS |
| Data scaling software | SCALA |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 20.000 | 2.740 |
| High resolution limit [Å] | 2.600 | 2.600 |
| Rmerge | 0.197 | 0.859 |
| Number of reflections | 5645 | 813 |
| <I/σ(I)> | 6.2 | 1.7 |
| Completeness [%] | 99.8 | |
| Redundancy | 8.3 | |
| CC(1/2) | 0.987 | 0.871 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 291 | PEG 8000, zinc acetate, buffer MES |






