5BR4
E. coli lactaldehyde reductase (FucO) M185C mutant
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRL BEAMLINE BL12-2 |
| Synchrotron site | SSRL |
| Beamline | BL12-2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2014-06-04 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.7749 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 69.697, 63.769, 91.674 |
| Unit cell angles | 90.00, 111.15, 90.00 |
Refinement procedure
| Resolution | 85.500 - 0.910 |
| R-factor | 0.12999 |
| Rwork | 0.129 |
| R-free | 0.14747 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1rrm |
| RMSD bond length | 0.021 |
| RMSD bond angle | 2.037 |
| Data reduction software | XDS |
| Data scaling software | SCALA (3.3.21) |
| Phasing software | MOLREP |
| Refinement software | REFMAC (5.8.0069) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 85.500 | 36.534 | 0.960 |
| High resolution limit [Å] | 0.909 | 2.870 | 0.910 |
| Rmerge | 0.015 | 2.250 | |
| Rmeas | 0.077 | ||
| Rpim | 0.044 | 0.011 | 1.669 |
| Total number of observations | 1333897 | 45192 | 145409 |
| Number of reflections | 491073 | ||
| <I/σ(I)> | 8.8 | 54 | 0.4 |
| Completeness [%] | 91.8 | 94.9 | 74.6 |
| Redundancy | 2.7 | 2.8 | 2.5 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 295 | 12% PEG3350, 200 mM ammonium chloride |






