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Literature summary for 3.2.1.146 extracted from

  • Bordoni, A.; de Lederkremer, R.M.; Marino, C.
    Synthesis of 5-deoxy-beta-D-galactofuranosides as tools for the characterization of beta-D-galactofuranosidases (2010), Bioorg. Med. Chem., 18, 5339-5345.
    View publication on PubMed
Search for more literature for 3.2.1.146

Inhibitors

Inhibitors Comment Organism Structure
4-methylphenyl 1-thio-beta-D-galactofuranoside low inhibitory activity with 30% inhibition at 0.25 mM Penicillium fellutanum
additional information no inhibition at concentrations up to 2.5 mM 4-methylphenyl 5-deoxy-1-thio-beta-D-galactofuranoside Penicillium fellutanum

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.31
-
 4-nitrophenyl beta-D-galactofuranoside in 66 mM NaOAc buffer (pH 4.9), at 37°C Penicillium fellutanum
1.29
-
 4-nitrophenyl 5-deoxy-beta-D-galactofuranoside in 66 mM NaOAc buffer (pH 4.9), at 37°C Penicillium fellutanum

Organism

Organism UniProt Comment Textmining
Penicillium fellutanum
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
4-nitrophenyl 5-deoxy-beta-D-galactofuranoside + H2O substrate with low affinity Penicillium fellutanum ?
-
 ?
4-nitrophenyl beta-D-galactofuranoside + H2O
-
 Penicillium fellutanum 4-nitrophenol + beta-D-galactofuranose
-
 ?
additional information no hydrolysis of 4-methylumbelliferyl beta-D-galactofuranoside and methyl 5-deoxy-alpha-L-arabino-hexofuranoside Penicillium fellutanum ?
-
 ?

Synonyms

Synonyms Comment Organism
exo-beta-D-galactofuranosidase
-
 Penicillium fellutanum