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Literature summary for 1.13.11.53 extracted from

  • Szajna, E.; Arif, A.M.; Berreau, L.M.
    Aliphatic carbon-carbon bond cleavage reactivity of a mononuclear Ni(II) cis-beta-keto-enolate complex in the presence of base and O2: a model reaction for acireductone dioxygenase (ARD) (2005), J. Am. Chem. Soc., 127, 17186-17187.
    View publication on PubMed

Metals/Ions

Metals/Ions Comment Organism Structure
Ni2+ Ni2+-containg enzyme Klebsiella pneumoniae

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1,2-dihydroxy-5-(methylthio)pent-1-en-3-one + O2 Klebsiella pneumoniae reaction is a shunt out of the methionine salvage pathway 3-(methylthio)propanoate + formate + CO
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Organism

Organism UniProt Comment Textmining
Klebsiella pneumoniae
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1,2-dihydroxy-5-(methylthio)pent-1-en-3-one + O2 reaction is a shunt out of the methionine salvage pathway Klebsiella pneumoniae 3-(methylthio)propanoate + formate + CO
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additional information aliphatic carbon-carbon bond cleavage reactivity of a mononuclear Ni(II) cis-beta-keto-enolate complex in the presence of base and O2: a model reaction for acireductone dioxygenase Klebsiella pneumoniae ?
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Synonyms

Synonyms Comment Organism
ARD
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Klebsiella pneumoniae