1D7K
CRYSTAL STRUCTURE OF HUMAN ORNITHINE DECARBOXYLASE AT 2.1 ANGSTROMS RESOLUTION
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CHESS BEAMLINE A1 |
Synchrotron site | CHESS |
Beamline | A1 |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 1996-01-15 |
Detector | FUJI |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 61.680, 107.450, 139.710 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 30.500 - 2.100 |
Rwork | 0.212 |
R-free | 0.28800 |
RMSD bond length | 0.016 |
RMSD bond angle | 2.500 |
Data reduction software | DENZO |
Data scaling software | CCP4 ((SCALA)) |
Phasing software | AMoRE |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.160 |
High resolution limit [Å] | 2.100 | 2.090 |
Rmerge | 0.068 | 0.363 |
Total number of observations | 223151 * | |
Number of reflections | 53656 | |
<I/σ(I)> | 10.1 | |
Completeness [%] | 96.4 | 97.5 |
Redundancy | 4 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | unknown * | 7.5 | 289 | 20% PEG 3350, 0.2M NaCl, 5mM DTT, 0.1M Tris-HCl, pH 7.5, VAPOR DIFFUSION, temperature 16K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | 1 | protein | 20 (mg/ml) | |
2 | 1 | 2 | PEG3350 | 20 (%(w/v)) | |
3 | 1 | 2 | Tris-HCl | 0.1 (M) | |
4 | 1 | 2 | 0.2 (M) |