9XPR
Maltose-binding protein
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SPRING-8 BEAMLINE BL26B1 |
| Synchrotron site | SPring-8 |
| Beamline | BL26B1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2025-07-19 |
| Detector | DECTRIS EIGER R 4M |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 70.443, 64.765, 82.507 |
| Unit cell angles | 90.00, 97.25, 90.00 |
Refinement procedure
| Resolution | 33.520 - 1.600 |
| R-factor | 0.1939 |
| Rwork | 0.192 |
| R-free | 0.23080 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | AlphaFold |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.825 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHENIX |
| Refinement software | PHENIX ((1.21.1_5286: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 47.500 | 1.630 |
| High resolution limit [Å] | 1.600 | 1.600 |
| Rmeas | 0.027 | 0.794 |
| Rpim | 0.017 | 0.490 |
| Number of reflections | 96832 | 4579 |
| <I/σ(I)> | 19.7 | 1.8 |
| Completeness [%] | 99.7 | 96.3 |
| Redundancy | 4.5 | 4.6 |
| CC(1/2) | 1.000 | 0.779 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 7.5 | 293 | 1.4 M sodium citrate |






