3A6H
W154A mutant creatininase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE BL-6A |
Synchrotron site | Photon Factory |
Beamline | BL-6A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-06-17 |
Detector | ADSC QUANTUM 4r |
Wavelength(s) | 1.00 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 106.800, 60.240, 146.200 |
Unit cell angles | 90.00, 100.30, 90.00 |
Refinement procedure
Resolution | 20.000 - 2.000 |
Rwork | 0.199 |
R-free | 0.23100 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1j2t |
RMSD bond length | 0.005 |
RMSD bond angle | 1.230 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | CNS |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.000 | 2.110 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.068 | 0.307 |
Number of reflections | 121694 | |
<I/σ(I)> | 12 | 3.1 |
Completeness [%] | 98.1 | 95.3 |
Redundancy | 3 | 2.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6 | 293 | 42% PEG200, 10mM Magnesium chloride, 100mM cacodylate buffer, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K |