2BTY
Acetylglutamate kinase from Thermotoga maritima complexed with its inhibitor arginine
Replaces: 1UVVExperimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-2 |
Synchrotron site | ESRF |
Beamline | ID14-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2001-10-22 |
Detector | ADSC CCD |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 94.998, 207.709, 117.996 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.950 - 2.750 |
R-factor | 0.242 |
Rwork | 0.242 |
R-free | 0.27300 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1buf |
RMSD bond length | 0.009 |
RMSD bond angle | 1.700 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | CNS (1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 2.850 |
High resolution limit [Å] | 2.750 | 2.750 |
Rmerge | 0.060 | 0.360 |
Number of reflections | 30394 | |
<I/σ(I)> | 22 | 4.1 |
Completeness [%] | 98.8 | 98.4 |
Redundancy | 3.2 | 3.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 4.6 | 15% POLYETHYLENE GLYCOL 4K, SODIUM ACETATE 50 MM PH 4.6, AMMONIUM SULFATE 75 MM |