1B05
Structure of oligo-peptide binding protein complexed with LYS-CYS-LYS
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Temperature [K] | 120 |
Detector technology | IMAGE PLATE |
Detector | MARRESEARCH |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 109.550, 76.120, 70.500 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 15.000 - 2.000 |
R-factor | 0.198 * |
Rwork | 0.198 |
R-free | 0.24300 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1OLB |
RMSD bond length | 0.013 |
RMSD bond angle | 0.033 |
Data reduction software | DENZO |
Data scaling software | SCALA |
Phasing software | CCP4 |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 15.000 | 2.120 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.100 * | 0.188 |
Number of reflections | 40411 | |
<I/σ(I)> | 6.6 | 3.4 |
Completeness [%] | 96.2 | 80.3 |
Redundancy | 4.3 | 4.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 5.5 | CO-CRYSTALLIZED WITH URANIUM ACETATE, PH 5.5 |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | PEG4000 | 5-10 (%(w/v)) | |
2 | 1 | drop | sodium acetate | 50 (mM) | |
3 | 1 | drop | uranyl acetate | 1 (mM) | |
4 | 1 | drop | peptide | 30 (mg/ml) |