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 |