7KBR
Co-crystal structure of alpha glucosidase with compound 10
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 23-ID-B |
| Synchrotron site | APS |
| Beamline | 23-ID-B |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2020-04-08 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9793 |
| Spacegroup name | P 32 |
| Unit cell lengths | 102.815, 102.815, 240.552 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 42.330 - 2.090 |
| R-factor | 0.1637 |
| Rwork | 0.163 |
| R-free | 0.18600 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5f0e |
| Data reduction software | HKL-2000 (v717.1) |
| Data scaling software | HKL-2000 (v717.1) |
| Phasing software | PHENIX (1.18.2_3874) |
| Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 42.330 | 2.169 |
| High resolution limit [Å] | 2.090 | 2.090 |
| Rmerge | 0.131 | 0.960 |
| Rmeas | 0.140 | 1.034 |
| Rpim | 0.048 | 0.380 |
| Number of reflections | 166814 | 16182 |
| <I/σ(I)> | 10.57 | 1.22 |
| Completeness [%] | 99.5 | 97.06 |
| Redundancy | 8.3 | 7.2 |
| CC(1/2) | 0.993 | 0.683 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7 | 297 | 0.09M NPS, 0.1M Buffer system 1 pH 7.0, 29%v/v P500MME_P20K |






