1VIV
Crystal structure of a hypothetical protein
Experimental procedure
| Experimental method | MAD |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 32-ID |
| Synchrotron site | APS |
| Beamline | 32-ID |
| Detector technology | CCD |
| Detector | MARRESEARCH |
| Wavelength(s) | 0.9794, 0.9794 |
| Spacegroup name | P 65 2 2 |
| Unit cell lengths | 71.363, 71.363, 245.452 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 35.680 - 2.600 |
| Rwork | 0.277 |
| R-free | 0.33100 |
| Structure solution method | Se-Met MAD phasing |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.200 * |
| Data reduction software | MOSFLM |
| Data scaling software | SCALA |
| Refinement software | REFMAC (4.0) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 35.680 | 2.450 |
| High resolution limit [Å] | 2.320 | 2.320 |
| Rmerge | 0.057 | 0.294 |
| Number of reflections | 16522 | |
| <I/σ(I)> | 24.7 | 6.2 |
| Completeness [%] | 98.2 | 88.4 |
| Redundancy | 14.4 | 9.8 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Vapor diffusion, hanging drop * | 7.5 * |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | drop | HEPES | 10 (mM) | pH7.5 |
| 2 | 1 | drop | 150 (mM) | ||
| 3 | 1 | drop | methionine | 10 (mM) | |
| 4 | 1 | drop | glycerol | 10 (%) | |
| 5 | 1 | drop | dithiothreitol | 5 (mM) | |
| 6 | 1 | drop | protein | 10 (mg/ml) |
