1JF6
Crystal structure of thermoactinomyces vulgaris r-47 alpha-amylase mutant F286Y
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 | 2000-11-27 |
| Detector | ADSC QUANTUM 4 |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 112.250, 117.940, 113.320 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 38.390 - 3.200 |
| R-factor | 0.204 |
| Rwork | 0.204 |
| R-free | 0.28300 * |
| RMSD bond length | 0.010 |
| RMSD bond angle | 24.800 * |
| Data reduction software | MOSFLM |
| Data scaling software | CCP4 ((SCALA)) |
| Phasing software | CNS |
| Refinement software | CNS |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 30.000 * |
| High resolution limit [Å] | 3.200 |
| Rmerge | 0.121 |
| Total number of observations | 131344 * |
| Number of reflections | 23309 |
| <I/σ(I)> | 5.8 |
| Completeness [%] | 91.7 |
| Redundancy | 5.2 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 6.1 | 11 * | Kamitori, S., (1999) J.Mol.Biol., 287, 907. * |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | reservoir | PEG6000 | 2 (%(w/v)) | |
| 2 | 1 | reservoir | 2.5 (mM) | ||
| 3 | 1 | reservoir | MES | 20 (mM) | |
| 4 | 1 | drop | protein | 20 (mg/ml) |






