2JFP
Crystal structure of Enterococcus faecalis glutamate racemase in complex with D- Glutamate
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MAX II BEAMLINE I711 |
Synchrotron site | MAX II |
Beamline | I711 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2003-05-28 |
Detector | MARRESEARCH |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 48.190, 74.670, 75.070 |
Unit cell angles | 90.00, 95.97, 90.00 |
Refinement procedure
Resolution | 34.000 - 1.980 |
Rwork | 0.204 |
R-free | 0.24600 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2jfo |
RMSD bond length | 0.006 |
RMSD bond angle | 1.272 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | CNX (2002.2) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 34.000 | 2.080 |
High resolution limit [Å] | 1.980 | 1.980 |
Rmerge | 0.070 | 0.250 |
Number of reflections | 36578 | |
<I/σ(I)> | 4.9 | 2.5 |
Completeness [%] | 97.9 | 86.7 |
Redundancy | 3.4 | 3.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | PROTEIN FORMULATED AT 10 MG/ML WITH 200MM AMMONIUM ACETATE PH 7.4, 5MM D-L GLUTAMATE, 1 MM TCEP AND CRYSTALLISED WITH 0.1 M TRIS PH 7.5 0.2 MM CACL2 AND 20-25% PEG 3350 |