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Literature summary for 3.2.1.18 extracted from

  • Nees, S.; Veh, R.W.; Schauer, R.; Ehrlich, K.
    Purification and characterization of neuraminidase from Clostridium perfringens (1975), Hoppe-Seyler's Z. Physiol. Chem., 356, 1027-1042.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
Cu2+
-
Clostridium perfringens

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
60000 69000 gel filtration, ultracentrifugation, SDS-PAGE Clostridium perfringens

Organism

Organism UniProt Comment Textmining
Clostridium perfringens
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
Clostridium perfringens

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
615
-
sialyllactose as substrate Clostridium perfringens

Storage Stability

Storage Stability Organism
-20°C, 0.1 M KCN, six months Clostridium perfringens

Subunits

Subunits Comment Organism
monomer SDS-PAGE Clostridium perfringens

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
4.3 5.2
-
Clostridium perfringens

pH Range

pH Minimum pH Maximum Comment Organism
4 11
-
Clostridium perfringens