2ACY
ACYL-PHOSPHATASE (COMMON TYPE) FROM BOVINE TESTIS
Experimental procedure
Source type | ROTATING ANODE |
Source details | SIEMENS |
Temperature [K] | 277 |
Detector technology | IMAGE PLATE |
Collection date | 1995-08 |
Detector | MARRESEARCH |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 63.200, 36.200, 45.300 |
Unit cell angles | 90.00, 104.10, 90.00 |
Refinement procedure
Resolution | 15.000 - 1.800 |
R-factor | 0.17 |
Rwork | 0.179 |
R-free | 0.23500 * |
Structure solution method | MIR |
RMSD bond length | 0.010 |
RMSD bond angle | 16.900 * |
Data reduction software | MARXDS |
Data scaling software | MARSCALE |
Phasing software | MLPHARE |
Refinement software | TNT (5E) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.900 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.059 | 0.215 |
Total number of observations | 41285 * | |
Number of reflections | 8949 | |
<I/σ(I)> | 36.98 | 10.52 |
Completeness [%] | 98.8 | 92.4 |
Redundancy | 4.6 | 1.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 3.5 | 4 * | PROTEIN WAS CRYSTALLIZED FROM 30% PEG8000 OR 4000, 25 MM ACETATE BUFFER PH 3.5, 0.2 M AMMONIUM-SULFATE |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | acetate | 25 (mM) | |
2 | 1 | reservoir | PEG4000 | 30 (%) | |
3 | 1 | reservoir | ammonium sulfate | 0.2 (M) |