1D5E
The role of phenylalanine 8 in the stabilization of the S protein-S peptide interaction: Packing and cavities
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 293 |
Detector technology | IMAGE PLATE |
Collection date | 1999-08-27 |
Detector | MARRESEARCH |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 44.600, 44.600, 98.070 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 10.000 - 2.250 |
R-factor | 0.209 |
Rwork | 0.209 |
R-free | 0.23100 |
RMSD bond length | 0.006 |
RMSD bond angle | 1.600 |
Data reduction software | AUTOMAR |
Data scaling software | XDS |
Phasing software | X-PLOR |
Refinement software | X-PLOR (3.851) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 10.000 | 2.300 |
High resolution limit [Å] | 2.200 | 2.200 |
Rmerge | 0.096 | 0.450 |
Number of reflections | 4923 * | |
<I/σ(I)> | 11.1 | |
Completeness [%] | 98.0 | 95 |
Redundancy | 6 | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | unknown * | 5.75 | 20 * | Thomson, J., (1994) Biochemistry, 33, 8587. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 4-5 (mg/ml) | |
2 | 1 | drop | 3 (M) | ||
3 | 1 | drop | acetate | 0.1 (M) | |
4 | 1 | drop | ammonium sulfate | 35 (%) |