1KGQ
Crystal Structure of Tetrahydrodipicolinate N-Succinyltransferase in Complex with L-2-aminopimelate and Succinamide-CoA
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 298 |
Detector technology | AREA DETECTOR |
Collection date | 1999-04-26 |
Detector | XENTRONICS |
Wavelength(s) | 1.5418 |
Spacegroup name | H 3 |
Unit cell lengths | 95.840, 95.840, 72.640 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 99.000 - 2.000 |
R-factor | 0.179 |
Rwork | 0.174 |
R-free | 0.25000 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.022 |
RMSD bond angle | 2.200 |
Data reduction software | X-GEN |
Data scaling software | XDS |
Phasing software | TNT |
Refinement software | TNT |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 99.000 | 2.100 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.048 | 0.217 |
Total number of observations | 59293 * | |
Number of reflections | 16693 | |
Completeness [%] | 99.5 | 97.9 |
Redundancy | 3.5 * |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 * | 298 | Binder, D.A., (1996) Proteins, 26, 115. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 25 (mg/ml) | |
2 | 1 | drop | HEPES | 20 (mM) | pH7.5 |
3 | 1 | reservoir | PEG4000 | 12 (%) | |
4 | 1 | reservoir | ammonium sulfate | 200 (mM) | |
5 | 1 | reservoir | MES | 100 (mM) | pH6.2 |
6 | 1 | reservoir | CoA | 2.5 (mM) | |
7 | 1 | reservoir | 2-aminopimelate | 16 (mM) |