2AAW
Studies on ligand binding and enzyme inhibition of Plasmodium falciparum glutathione S-transferase
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 | 2003-07-05 |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 0.93927 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 61.170, 69.990, 123.690 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 14.990 - 2.400 |
R-factor | 0.194 |
Rwork | 0.194 |
R-free | 0.23700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1okt |
RMSD bond length | 0.006 |
RMSD bond angle | 1.200 |
Data reduction software | CAD4 |
Data scaling software | XDS |
Phasing software | CNS |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 14.990 | 2.550 |
High resolution limit [Å] | 2.400 | 2.400 |
Number of reflections | 20939 | |
Completeness [%] | 97.7 | 84.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 298 | PEG400, CaCl2, NaHepes, S-hexylglutathione, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K |