1O8F
Pectate Lyase C from Erwinia Chrysanthemi at pH 9.5 with 30mM Ca2+
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RT3000 |
Temperature [K] | 293 |
Detector technology | AREA DETECTOR |
Detector | SDMS |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 72.710, 80.800, 95.740 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 10.000 - 2.200 |
R-factor | 0.1841 |
Rwork | 0.184 |
R-free | 0.23020 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1air |
RMSD bond length | 0.008 |
RMSD bond angle | 24.710 * |
Data reduction software | SDMS |
Data scaling software | SDMS |
Phasing software | X-PLOR |
Refinement software | X-PLOR (3.851) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 10.000 |
High resolution limit [Å] | 2.200 |
Rmerge | 0.063 |
Total number of observations | 178014 * |
Number of reflections | 42615 |
<I/σ(I)> | 7.79 |
Completeness [%] | 99.8 |
Redundancy | 4.18 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, sitting drop * | 6.9 * | 4 * | Yoder, M. D., (1990) J. Biol. Chem., 265, 11429. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 5 (A280/ml) | |
2 | 1 | drop | ammonium sulfate | 1.0 (M) | |
3 | 1 | drop | HEPES | 50 (mM) | |
4 | 1 | drop | 1 (mM) | ||
5 | 1 | reservoir | ammonium sulfate | 2.0 (M) | |
6 | 1 | reservoir | HEPES | 0.1 (M) |