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Literature summary extracted from

  • Zalkin, H.
    NAD synthetase (1985), Methods Enzymol., 113, 297-302.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
6.3.1.5 Decoyinine
-
 Escherichia coli
6.3.1.5 Psicofuranine i.e. 9-D-psicofuranosyl-6-aminopurine, each substrate provides some protection Escherichia coli

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
6.3.1.5 0.065
-
 NH3
-
 Escherichia coli
6.3.1.5 0.11
-
 deamido-NAD+
-
 Escherichia coli
6.3.1.5 0.2
-
 ATP
-
 Escherichia coli
6.3.1.5 5
-
 Gln
-
 Escherichia coli

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
6.3.1.5 ATP + deamido-NAD+ + NH3 Escherichia coli
-
 ?
-
 ?

Organism

EC Number Organism UniProt Comment Textmining
6.3.1.5 Escherichia coli
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
6.3.1.5
-
 Escherichia coli

Specific Activity [micromol/min/mg]

EC Number Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
6.3.1.5 6.9
-
-
 Escherichia coli

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
6.3.1.5 ATP + deamido-NAD+ + NH3 NH3 is the preferred nitrogen donor Escherichia coli AMP + diphosphate + NAD+
-
 ?
6.3.1.5 ATP + deamido-NAD+ + NH3
-
 Escherichia coli ?
-
 ?