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Literature summary for 3.2.1.40 extracted from

  • Provencher, L.; Steensma, D.H.; Wong, C.H.
    Five-membered ring azasugars as potent inhibitors of alpha-L-rhamnosidase (naringinase) from Penicillium decumbens (1994), Bioorg. Med. Chem., 2, 1179-1188.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
five-membered ring azasugars with L-rhamnose configuration, substitution at the nitrogen shifts the inhibition mechanism from mixed to competitive Penicillium sp.

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
alpha-L-rhamnoside + H2O Penicillium sp. alpha-L-rhamnose in glycolipids or glycosides alpha-L-rhamnose + ?
-
?

Organism

Organism UniProt Comment Textmining
Penicillium sp.
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
alpha-L-rhamnoside + H2O alpha-L-rhamnose in glycolipids or glycosides Penicillium sp. alpha-L-rhamnose + ?
-
?
p-nitrophenyl alpha-L-rhamnoside + H2O
-
Penicillium sp. p-nitrophenol + alpha-L-rhamnose
-
?