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Literature summary for 3.2.1.28 extracted from

  • Temesvari, L.A.; Cotter, D.A.
    Trehalase of Dictyostelium discoideum: inhibition by amino-containing analogs of trehalose and affinity purification (1997), Biochimie, 79, 229-239.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
castanospermine potent, reversible, competitive Dictyostelium discoideum
MDL 25 637 i.e. 7-O-beta-D-glucopyranosyl-alpha-homojirimycin; potent, reversible, competitive, slow-binding nature Dictyostelium discoideum
validamycin A potent, reversible, competitive, slow-binding nature Dictyostelium discoideum

Organism

Organism UniProt Comment Textmining
Dictyostelium discoideum
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
Dictyostelium discoideum

Source Tissue

Source Tissue Comment Organism Textmining
vegetative
-
Dictyostelium discoideum
-

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
2000
-
-
Dictyostelium discoideum

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
trehalose + H2O
-
Dictyostelium discoideum D-glucose
-
?

Subunits

Subunits Comment Organism
More a major protein species of 42000 Da and two minor protein species of 45000 Da and 49000 Da are detected by SDS-PAGE Dictyostelium discoideum