7C64
Crystal structure of beta-glycosides-binding protein of ABC transporter in an open state (Form II)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | ROTATING ANODE |
| Source details | RIGAKU MICROMAX-007 HF |
| Temperature [K] | 100 |
| Detector technology | IMAGE PLATE |
| Collection date | 2018-12-29 |
| Detector | RIGAKU RAXIS IV++ |
| Wavelength(s) | 1.5418 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 57.460, 100.710, 66.260 |
| Unit cell angles | 90.00, 104.19, 90.00 |
Refinement procedure
| Resolution | 50.360 - 1.630 |
| R-factor | 0.1342 |
| Rwork | 0.133 |
| R-free | 0.16580 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 7c63 |
| RMSD bond length | 0.021 |
| RMSD bond angle | 2.380 |
| Data reduction software | MOSFLM (7.2.2) |
| Data scaling software | Aimless (0.7.4) |
| Phasing software | PHASER (2.8.3) |
| Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.360 | 50.350 | 1.660 |
| High resolution limit [Å] | 1.630 | 8.920 | 1.630 |
| Rmerge | 0.049 | 0.025 | 0.189 |
| Rmeas | 0.055 | 0.028 | 0.217 |
| Rpim | 0.025 | 0.012 | 0.103 |
| Total number of observations | 2653 | 18698 | |
| Number of reflections | 91079 | 587 | 4434 |
| <I/σ(I)> | 19.3 | 33.8 | 6.5 |
| Completeness [%] | 99.9 | 99.5 | 98 |
| Redundancy | 4.6 | 4.5 | 4.2 |
| CC(1/2) | 0.998 | 0.999 | 0.963 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | MICROBATCH | 293 | 0.2 M Ammonium sulphate, 70% PEG 8000 |






