5G53
Structure of the adenosine A2A receptor bound to an engineered G protein
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-2 |
Synchrotron site | ESRF |
Beamline | ID23-2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-04-09 |
Detector | DECTRIS PILATUS 2M |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 90.632, 111.814, 161.304 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 91.890 - 3.400 |
R-factor | 0.28537 |
Rwork | 0.284 |
R-free | 0.31542 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB ENTRIES 2YDV 3sn6 |
RMSD bond length | 0.008 |
RMSD bond angle | 1.149 |
Data reduction software | MOSFLM |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0144) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.300 | 3.490 |
High resolution limit [Å] | 3.400 | 3.400 |
Rmerge | 0.170 | 0.750 |
Number of reflections | 20898 | |
<I/σ(I)> | 3.6 | 1.2 |
Completeness [%] | 90.6 | 78.5 |
Redundancy | 2.6 | 2.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 5.5 | 0.1 M NAOAC PH 5.5, 10% PEG 2000 (IN THE PRESENCE OF CHS); OR 0.1 M NAOAC PH 5.7, 9.5% PEG 2000 MME (IN THE ABSENCE OF CHS) |