2C12
Crystal Structure of Nitroalkane Oxidase in Complex with Spermine, a Competitive Inhibitor
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 14-BM-C |
Synchrotron site | APS |
Beamline | 14-BM-C |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2003-08-09 |
Detector | ADSC CCD |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 103.393, 103.393, 485.134 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 50.000 - 2.070 |
R-factor | 0.19 |
Rwork | 0.188 |
R-free | 0.22500 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2c0u |
RMSD bond length | 0.013 |
RMSD bond angle | 1.394 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | MOLREP |
Refinement software | REFMAC (5.1.24) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.150 |
High resolution limit [Å] | 2.070 | 2.070 |
Rmerge | 0.140 | 0.269 |
Number of reflections | 180533 | |
<I/σ(I)> | 12.6 | 3 |
Completeness [%] | 97.8 | 81.9 |
Redundancy | 1.64 | 1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | 25%(W/V) PEG 4000, 35% (V/V) GLYCEROL, 200 MM SODIUM CACODYLATE TRIHYDRATE PH 7.5, 1 MM SPERMINE TETRAHYDROCHLORIDE |