2QLL
Human liver glycogen phosphorylase- GL complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2003-04-01 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.9 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 123.986, 123.986, 125.695 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.500 - 2.560 |
R-factor | 0.206 |
Rwork | 0.203 |
R-free | 0.27600 |
Structure solution method | FOURIER SYNTHESIS |
RMSD bond length | 0.008 |
RMSD bond angle | 1.120 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.500 | 2.710 |
High resolution limit [Å] | 2.560 | 2.560 |
Rmerge | 0.075 | 0.471 |
Number of reflections | 37156 | |
<I/σ(I)> | 12.47 | 3.1 |
Completeness [%] | 98.6 | 99.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 293 | 8 mg/ml protein, 0.1 M TRIS, 8% PEG 8000, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K |