1AQT
EPSILON SUBUNIT OF F1F0-ATP SYNTHASE FROM ESCHERICHIA COLI
Experimental procedure
Source type | ROTATING ANODE |
Source details | RIGAKU RUH2R |
Temperature [K] | 293 |
Detector technology | IMAGE PLATE |
Collection date | 1994-09 |
Detector | RIGAKU RAXIS II |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 94.610, 94.610, 56.920 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.000 - 2.300 |
R-factor | 0.214 |
Rwork | 0.214 |
R-free | 0.28800 |
Structure solution method | MULTIPLE ISOMORPHOUS REPLACEMENT |
RMSD bond length | 0.010 |
RMSD bond angle | 1.500 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | X-PLOR (3.843) |
Refinement software | X-PLOR (3.843) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.000 | 2.380 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.059 * | 0.475 * |
Total number of observations | 19833 * | |
Number of reflections | 6626 | |
<I/σ(I)> | 12.4 | 1.8 |
Completeness [%] | 94.0 | 89 |
Redundancy | 3 | 2.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 7.5 | PROTEIN (4 MG/ML)IN 50 MM HEPES BUFFER, PH 7.5, 200 MM (NH2)2SO4, 2 M (NA/K)PO4 |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | 2 (M) | ||
2 | 1 | reservoir | HEPES | 100 (mM) | |
3 | 1 | reservoir | 200 (mM) | ||
4 | 1 | drop | protein | 2 (mg/ml) | |
5 | 1 | drop | 1 (M) | ||
6 | 1 | drop | HEPES | 50 (mM) | |
7 | 1 | drop | 100 (mM) |