4A6T
Crystal structure of the omega transaminase from Chromobacterium violaceum in complex with PLP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MAX II BEAMLINE I911-2 |
Synchrotron site | MAX II |
Beamline | I911-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-05-06 |
Detector | MARRESEARCH SX-165 |
Spacegroup name | P 1 |
Unit cell lengths | 61.490, 62.320, 119.520 |
Unit cell angles | 105.44, 90.90, 104.52 |
Refinement procedure
Resolution | 29.339 - 1.800 |
R-factor | 0.1666 |
Rwork | 0.165 |
R-free | 0.20190 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4a6r |
RMSD bond length | 0.005 |
RMSD bond angle | 1.008 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 1.790 |
High resolution limit [Å] | 1.700 | 1.700 |
Rmerge | 0.070 | 0.380 |
Number of reflections | 210786 | |
<I/σ(I)> | 12.7 | 3.7 |
Completeness [%] | 93.5 | 83.6 |
Redundancy | 2.7 | 2.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.4 | DROPS OF 200 UL PROTEIN AT 12 MG/ML MIXED WITH 200 UL OF 0.1 M HEPES PH 7.5, 150-300 MM NACL AND 22.5-27.5% PEG 4000. |