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Literature summary extracted from

  • Hayaishi, O.; Tabor, H.; Hayaishi, T
    N-Formimino-L-aspartic acid as an intermediate in the enzymic conversion of imidazoleacetic acid to formylaspartic acid (1957), J. Biol. Chem., 227, 161-180.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.5.3.5 p-chloromercuribenzoate 0.00025 M, 25% inhibition Pseudomonas sp.

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
3.5.3.5 N-formimino-L-aspartic acid + H2O Pseudomonas sp.
-
 N-formylaspartic acid + NH3
-
 ?

Organism

EC Number Organism UniProt Comment Textmining
3.5.3.5 Pseudomonas sp.
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
3.5.3.5
-
 Pseudomonas sp.

Specific Activity [micromol/min/mg]

EC Number Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
3.5.3.5 10.8
-
-
 Pseudomonas sp.

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.5.3.5 additional information formiminoglutamic acid and formiminoglycine are no substrates Pseudomonas sp. ?
-
 ?
3.5.3.5 N-formimino-L-aspartic acid + H2O
-
 Pseudomonas sp. N-formylaspartic acid + NH3
-
 ?

Synonyms

EC Number Synonyms Comment Organism
3.5.3.5 FIA hydrolase
-
 Pseudomonas sp.

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
3.5.3.5 9
-
-
 Pseudomonas sp.