5OBH
Crystal structure of glycine binding protein in complex with bicuculline
Experimental procedure
| Experimental method | SINGLE WAVELENGTH | 
| Source type | ROTATING ANODE | 
| Source details | RIGAKU MICROMAX-007 HF | 
| Temperature [K] | 150 | 
| Detector technology | CCD | 
| Collection date | 2016-11-16 | 
| Detector | RIGAKU SATURN 944+ | 
| Wavelength(s) | 1.54157 | 
| Spacegroup name | P 21 21 21 | 
| Unit cell lengths | 71.243, 132.236, 132.631 | 
| Unit cell angles | 90.00, 90.00, 90.00 | 
Refinement procedure
| Resolution | 46.820 - 2.400 | 
| R-factor | 0.23054 | 
| Rwork | 0.230 | 
| R-free | 0.24944 | 
| Structure solution method | MOLECULAR REPLACEMENT | 
| Starting model (for MR) | 5oan | 
| RMSD bond length | 0.009 | 
| RMSD bond angle | 1.418 | 
| Data reduction software | XDS | 
| Data scaling software | Aimless | 
| Phasing software | PHASER | 
| Refinement software | REFMAC (5.8.0158) | 
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.820 | 2.480 | 
| High resolution limit [Å] | 2.400 | 2.400 | 
| Rmerge | 0.130 | 0.776 | 
| Number of reflections | 49817 | 4510 | 
| <I/σ(I)> | 7.9 | 1.8 | 
| Completeness [%] | 100.0 | 100 | 
| Redundancy | 6.2 | 6.2 | 
| CC(1/2) | 0.995 | 0.826 | 
Crystallization Conditions
| crystal ID | method | pH | temperature | details | 
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 293 | Reservoir buffer: 0.2 M ammonium formate, 20 % PEG 3350 Protein buffer: 50 mM tris, 250 mM NaCl, pH 7.5. 2 mM bicuculline | 











