5I3H
Structure-Function Studies on Role of Hydrophobic Clamping of a Basic Glutamate in Catalysis by Triosephosphate Isomerase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-06-04 |
Detector | RIGAKU SATURN 944+ |
Wavelength(s) | 1.5418 |
Spacegroup name | P 1 |
Unit cell lengths | 46.282, 46.656, 60.981 |
Unit cell angles | 72.68, 88.47, 80.60 |
Refinement procedure
Resolution | 28.470 - 2.250 |
R-factor | 0.1681 |
Rwork | 0.166 |
R-free | 0.21070 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3tim |
RMSD bond length | 0.002 |
RMSD bond angle | 0.617 |
Data reduction software | d*TREK |
Data scaling software | d*TREK |
Phasing software | MOLREP |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 28.470 | 2.299 |
High resolution limit [Å] | 2.250 | 2.250 |
Rmerge | 0.052 | |
Number of reflections | 23315 | |
<I/σ(I)> | 15.9 | |
Completeness [%] | 98.4 | |
Redundancy | 2.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 287 | 15-25% Peg 8000, 50-100 mM potassium acetate, 100 mM BTP pH 7.0 |