1DEO
RHAMNOGALACTURONAN ACETYLESTERASE FROM ASPERGILLUS ACULEATUS AT 1.55 A RESOLUTION WITH SO4 IN THE ACTIVE SITE
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU |
Temperature [K] | 291 |
Detector technology | IMAGE PLATE |
Collection date | 1995-04-25 |
Detector | RIGAKU RAXIS II |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 52.140, 56.870, 71.890 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 30.000 - 1.550 |
R-factor | 0.164 * |
Rwork | 0.164 |
R-free | 0.20000 |
RMSD bond length | 0.014 |
RMSD bond angle | 24.300 * |
Data reduction software | ROTAVATA |
Data scaling software | CCP4 ((AGROVATA) |
Phasing software | MLPHARE |
Refinement software | X-PLOR (3.851) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 1.630 |
High resolution limit [Å] | 1.550 | 1.550 |
Rmerge | 0.035 | 0.293 |
Number of reflections | 28693 | |
<I/σ(I)> | 13.7 | |
Completeness [%] | 91.0 | 77.9 |
Redundancy | 7.7 | 2.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | unknown * | 5 | 298 | Lithium sulfate, Na acetate, pH 5.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | 1 | 1.4 (M) | ||
2 | 1 | 1 | sodium acetate | 0.1 (M) | |
3 | 1 | 1 | protein | 40 (OD280) |