5C1C
Crystal Structure of the Pectin Methylesterase from Aspergillus niger in Deglycosylated Form
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU MICROMAX-007 |
Temperature [K] | 123 |
Detector technology | IMAGE PLATE |
Collection date | 2013-10-23 |
Detector | RIGAKU RAXIS IV++ |
Wavelength(s) | 1.5418 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 75.249, 113.843, 88.741 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 36.230 - 1.800 |
R-factor | 0.172 |
Rwork | 0.170 |
R-free | 0.20330 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1xg2 |
RMSD bond length | 0.007 |
RMSD bond angle | 1.258 |
Data reduction software | CrystalClear |
Data scaling software | d*TREK |
Phasing software | MrBUMP |
Refinement software | REFMAC (5.8.0073) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 36.230 | 1.860 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.075 | 0.313 |
Number of reflections | 34221 | |
<I/σ(I)> | 5.2 | 3.7 |
Completeness [%] | 95.7 | 91.4 |
Redundancy | 3.79 | 3.75 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.1 | 294 | Protein (6.5 mg/mL) in 50-100 mM acetate buffer mixed 1:1 with 1.8 M ammonium sulfate, 100 mM sodium acetate, pH 4.1 |