4UHN
Characterization of a Novel Transaminase from Pseudomonas sp. Strain AAC
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-06-28 |
Detector | ADSC CCD |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 62.912, 119.686, 134.257 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 89.340 - 2.210 |
R-factor | 0.14716 |
Rwork | 0.145 |
R-free | 0.18843 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4uhm |
RMSD bond length | 0.020 |
RMSD bond angle | 1.979 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0107) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 44.700 | 2.280 |
High resolution limit [Å] | 2.210 | 2.210 |
Rmerge | 0.270 | 1.120 |
Number of reflections | 25807 | |
<I/σ(I)> | 13.3 | 3.3 |
Completeness [%] | 100.0 | 100 |
Redundancy | 14.7 | 14.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8 | PROTEIN WAS AT 10 MG/ML AND WAS SET UP IN 200 NL PLUS 200 NL DROPS AGAINST 2.5 M NACL, 20 MM ZINC ACETATE, 0.1 M IMIDAZOLE BUFFER AT PH 8 |