2C21
Specificity of the Trypanothione-dependednt Leishmania major Glyoxalase I: Structure and biochemical comparison with the human enzyme
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-2 |
Synchrotron site | ESRF |
Beamline | ID14-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2004-10-16 |
Detector | ADSC CCD |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 130.193, 148.957, 50.698 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 129.100 - 2.000 |
R-factor | 0.157 |
Rwork | 0.155 |
R-free | 0.20100 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1fa8 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.248 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 60.000 | 2.110 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.050 | 0.300 |
Number of reflections | 67613 | |
<I/σ(I)> | 17.7 | 4.9 |
Completeness [%] | 99.8 | 99.5 |
Redundancy | 4.2 | 4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8 | 62% (V/V) MPD, 100MM TRIS-HCL PH 8.0 |