2JFX
Crystal structure of Helicobacter pylori glutamate racemase in complex with D-Glutamate
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 1997-12-16 |
Detector | MARRESEARCH |
Wavelength(s) | 0.9700 0.97821, 0.91834 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 62.180, 81.070, 113.820 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.000 - 2.300 |
Rwork | 0.228 |
R-free | 0.28080 |
Structure solution method | MAD |
RMSD bond length | 0.007 |
RMSD bond angle | 1.360 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | RANTAN (MLPHARE DM) |
Refinement software | CNX (2000.2) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 66.000 | 2.400 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.080 | 0.510 |
Number of reflections | 22893 | |
Completeness [%] | 87.2 | 79.4 |
Redundancy | 2.9 | 2.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | PROTEIN FORMULATED AT 10 MG/ML WAS CRYSTALLIZED WITH 100 MM TRIS PH 8.0, 25% PEG 3350, 80 MM MGCL2, 8% METHANOL, 10% GLYCEROL AND 5 MM DTT. |