1OBL
crystal structure of the S133A mutant of Malonamidase E2 complexed with malonate from Bradyrhizobium japonicum
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PAL/PLS BEAMLINE 6B |
Synchrotron site | PAL/PLS |
Beamline | 6B |
Temperature [K] | 100 |
Detector technology | CCD |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 103.629, 95.225, 74.981 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 52.000 - 2.000 |
R-factor | 0.188 |
Rwork | 0.188 |
R-free | 0.24500 |
Structure solution method | DIRECT METHODS |
Starting model (for MR) | 1GR8 |
RMSD bond length | 0.005 |
RMSD bond angle | 1.271 |
Data reduction software | SMART |
Data scaling software | PROSCALE |
Phasing software | CNS |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 52.083 |
High resolution limit [Å] | 2.000 |
Number of reflections | 46861 |
<I/σ(I)> | 7.16 |
Completeness [%] | 92.1 |
Redundancy | 5.07 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7 | 20% POLYETHYLENE GLYCOL 1000, 0.1 M TRIS-HCL, PH 7.0 |