2JFO
Crystal structure of Enterococcus faecalis glutamate racemase in complex with D- and L-Glutamate
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-4 |
Synchrotron site | ESRF |
Beamline | ID14-4 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2000-09-29 |
Detector | ADSC CCD |
Wavelength(s) | 0.9184 , 0.9786 , 0.9789 , 0.9184 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 60.290, 82.080, 111.570 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 20.000 - 2.500 |
Rwork | 0.204 |
R-free | 0.25670 |
Structure solution method | MAD |
RMSD bond length | 0.008 |
RMSD bond angle | 1.270 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | SOLVE |
Refinement software | CNX (2002.2) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 2.640 |
High resolution limit [Å] | 2.500 | 2.500 |
Rmerge | 0.120 | 0.330 |
Number of reflections | 18738 | |
<I/σ(I)> | 4.4 | 2.3 |
Completeness [%] | 95.6 | 96.2 |
Redundancy | 4.8 | 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 0.2 MM MGCL2 AND 20-25% PEG 4000 |