3T3E
Glycogen phosphorylase b in complex with GlcClU
Experimental procedure
Experimental method | Chryssalis |
Source type | SEALED TUBE |
Source details | OXFORD DIFFRACTION ENHANCE ULTRA |
Temperature [K] | 293 |
Detector technology | CCD |
Collection date | 2011-04-07 |
Detector | AGILENT ATLAS CCD |
Wavelength(s) | 1.5419 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 128.234, 128.234, 116.354 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 13.910 - 2.150 |
R-factor | 0.18007 |
Rwork | 0.177 |
R-free | 0.23267 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | 2gpn |
RMSD bond length | 0.021 |
RMSD bond angle | 1.900 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | REFMAC |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 13.940 | 2.270 |
High resolution limit [Å] | 2.150 | 2.150 |
Rmerge | 0.097 | 0.525 |
Number of reflections | 50243 | |
<I/σ(I)> | 9.9 | 2.4 |
Completeness [%] | 94.6 | 89.1 |
Redundancy | 3 | 2.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | SMALL TUBES | 6.7 | 289 | T state crystals soaked with 2 mM solution of the inhibitor in the crystallization media for 2hrs, pH 6.7, SMALL TUBES, temperature 289K |