1K97
Crystal Structure of E. coli Argininosuccinate Synthetase in complex with Aspartate and Citrulline
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Detector | MARRESEARCH |
Wavelength(s) | 1.5418 |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 77.996, 105.336, 127.360 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.000 * - 2.000 |
R-factor | 0.1757 * |
Rwork | 0.176 |
R-free | 0.21430 * |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1k91 |
RMSD bond length | 0.009 |
RMSD bond angle | 1.386 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | CNS |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.130 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.057 * | 0.265 * |
Number of reflections | 35667 | |
Completeness [%] | 99.3 | 97.6 * |
Redundancy | 7.8 * |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 * | 298 | Lemke, C., (1999) Acta Crystallogr., 55, 2028. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 10 (mg/ml) | |
2 | 1 | drop | Tris-HCl | 25 (mM) | pH7.5 |
3 | 1 | reservoir | ammonium sulfate | 1.5-1.6 (M) | |
4 | 1 | reservoir | MES | 100 (mM) | pH6.5 |