1HX0
Structure of pig pancreatic alpha-amylase complexed with the "truncate" acarbose molecule (pseudotrisaccharide)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID14-2 |
| Synchrotron site | ESRF |
| Beamline | ID14-2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 1999-11-20 |
| Detector | ADSC QUANTUM 4 |
| Wavelength(s) | 0.933 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 69.280, 113.550, 117.160 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 35.000 - 1.380 |
| R-factor | 0.1083 |
| Rwork | 0.108 |
| R-free | 0.13020 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1ppi |
| RMSD bond length | 0.013 * |
| RMSD bond angle | 0.030 * |
| Data reduction software | DENZO |
| Data scaling software | SCALA |
| Phasing software | AMoRE |
| Refinement software | SHELXL-97 |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 35.000 | 1.420 |
| High resolution limit [Å] | 1.380 | 1.380 |
| Rmerge | 0.067 | 0.451 * |
| Total number of observations | 507677 * | |
| Number of reflections | 184003 | |
| <I/σ(I)> | 13.1 | 1.93 |
| Completeness [%] | 97.0 | 96.13 |
| Redundancy | 2.8 | 2.3 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | batch | 8.5 | 277 | Qian, M., (1993) J. Mol. Biol., 232, 785. * |






