5J74
Fluorogen activating protein AM2.2 in complex with TO1-2p
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL11-1 |
Synchrotron site | SSRL |
Beamline | BL11-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-05-22 |
Detector | MARMOSAIC 325 mm CCD |
Wavelength(s) | 0.9794 |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 79.448, 114.830, 130.995 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 86.350 - 2.700 |
R-factor | 0.19951 |
Rwork | 0.197 |
R-free | 0.25039 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2b0s |
RMSD bond length | 0.009 |
RMSD bond angle | 1.493 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0135) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 86.350 | 2.760 |
High resolution limit [Å] | 2.700 | 2.700 |
Rmerge | 0.138 | 0.578 |
Number of reflections | 16728 | |
<I/σ(I)> | 14.3 | 3.3 |
Completeness [%] | 99.6 | 99 |
Redundancy | 6.1 | 6.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 298 | 32% PEG monomethyl ether 5000 0.2M potassium dihydrogen phosphate |