1B1H
OLIGO-PEPTIDE BINDING PROTEIN/TRIPEPTIDE (LYS HPE LYS) COMPLEX
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Temperature [K] | 120 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 109.722, 75.953, 70.424 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 20.000 - 1.800 |
| R-factor | 0.191 * |
| Rwork | 0.190 |
| R-free | 0.22000 |
| Structure solution method | OTHER |
| RMSD bond length | 0.009 |
| RMSD bond angle | 0.025 |
| Data reduction software | DENZO |
| Data scaling software | SCALA |
| Refinement software | REFMAC |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 20.000 | |
| High resolution limit [Å] | 1.800 | |
| Rmerge | 0.077 | 0.126 * |
| Total number of observations | 238371 * | |
| Number of reflections | 54469 | |
| <I/σ(I)> | 7 | |
| Completeness [%] | 98.7 * | 95.4 * |
| Redundancy | 4.4 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Vapor diffusion, hanging drop * | 5.5 | pH 5.50 |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | drop | protein | 25 (mg/ml) | |
| 2 | 1 | reservoir | PEG4000 | 7 (%) | |
| 3 | 1 | reservoir | uranyl acetate | 1 (mM) | |
| 4 | 1 | reservoir | sodium acetate | 50 (mM) |






