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Literature summary extracted from

  • Fetterolf, B.; Bewley, C.A.
    Synthesis of a bromotyrosine-derived natural product inhibitor of mycothiol-S-conjugate amidase (2004), Bioorg. Med. Chem. Lett., 14, 3785-3788.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.5.1.115 bromotyrosine oxime
-
Mycobacterium tuberculosis
3.5.1.115 hemibastidin-2
-
Mycobacterium tuberculosis
3.5.1.115 psammaplin A
-
Mycobacterium tuberculosis
3.5.1.115 verongamine
-
Mycobacterium tuberculosis

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
3.5.1.115 a mycothiol S-conjugate + H2O Mycobacterium tuberculosis
-
an N-acetyl L-cysteine-S-conjugate + 1-O-(2-amino-2-deoxy-alpha-D-glucopyranosyl)-1D-myo-inositol
-
?

Organism

EC Number Organism UniProt Comment Textmining
3.5.1.115 Mycobacterium tuberculosis
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.5.1.115 a mycothiol S-conjugate + H2O
-
Mycobacterium tuberculosis an N-acetyl L-cysteine-S-conjugate + 1-O-(2-amino-2-deoxy-alpha-D-glucopyranosyl)-1D-myo-inositol
-
?

Synonyms

EC Number Synonyms Comment Organism
3.5.1.115 MCA
-
Mycobacterium tuberculosis

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
3.5.1.115 0.03
-
pH and temperature not specified in the publication Mycobacterium tuberculosis bromotyrosine oxime