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Literature summary for 6.3.4.21 extracted from

  • Kosaka, A.; Spivey, H.O.; Gholson, R.K.
    Nicotinate phosphoribosyltransferase of yeast. Purification and properties (1971), J. Biol. Chem., 246, 3277-3283.
    View publication on PubMed

Activating Compound

Activating Compound Comment Organism Structure
additional information no activation by ADP Saccharomyces cerevisiae
additional information no activation by 3'-AMP, 5'-AMP Saccharomyces cerevisiae

General Stability

General Stability Organism
heat, unstable to, substrates protect Saccharomyces cerevisiae

Inhibitors

Inhibitors Comment Organism Structure
Mg2+ above 10 mM, significant pH alterations Saccharomyces cerevisiae
phosphate 0.1 M and above Saccharomyces cerevisiae

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.09
-
ATP
-
Saccharomyces cerevisiae

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+ requirement Saccharomyces cerevisiae
Mg2+ synergism with ATP Saccharomyces cerevisiae
Mg2+ 1-10 mM Saccharomyces cerevisiae
MgATP2-
-
Saccharomyces cerevisiae
phosphate activation, 0.01-0.1 M, in the presence of Mg2+ Saccharomyces cerevisiae

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
43000
-
gel filtration Saccharomyces cerevisiae

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
nicotinate + 5-phospho-alpha-D-ribose 1-diphosphate + ATP + H2O Saccharomyces cerevisiae first step in NAD+-(salvage) biosynthesis beta-nicotinate D-ribonucleotide + diphosphate + ADP + phosphate
-
?

Organism

Organism UniProt Comment Textmining
Saccharomyces cerevisiae
-
bakers´yeast
-

Purification (Commentary)

Purification (Comment) Organism
extraction, ammonium sulfate fractionation, chromatography on DEAE-cellulose and hydroxylapatite, 1000fold purified Saccharomyces cerevisiae

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
2.3
-
-
Saccharomyces cerevisiae

Storage Stability

Storage Stability Organism
-25°C, at least 1 month Saccharomyces cerevisiae

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
nicotinate + 5-phospho-alpha-D-ribose 1-diphosphate + ATP + H2O
-
Saccharomyces cerevisiae beta-nicotinate D-ribonucleotide + diphosphate + ADP + phosphate
-
?
nicotinate + 5-phospho-alpha-D-ribose 1-diphosphate + ATP + H2O first step in NAD+-(salvage) biosynthesis Saccharomyces cerevisiae beta-nicotinate D-ribonucleotide + diphosphate + ADP + phosphate
-
?

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
37
-
assay at Saccharomyces cerevisiae

Temperature Stability [°C]

Temperature Stability Minimum [°C] Temperature Stability Maximum [°C] Comment Organism
50
-
5 min: 95% loss of activity, MgATP2-, Mg-phosphoribose diphosphate, ATP, GTP or nicotinic acid protect, with 27%, 37%, 52%, 54% or 61% loss of activity, respectively. 10 min: 97% loss of activity, MgATP2-, Mg-5-phospho-alpha-D-ribose 1-diphosphate, ATP, GTP or nicotinic acid protect, with 43%, 52%, 60%, 63% or 69% loss of activity, respectively Saccharomyces cerevisiae

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
7.5 8.5 broad Saccharomyces cerevisiae

pH Range

pH Minimum pH Maximum Comment Organism
5.5 10 about half-maximal activity at pH 5.5 and 10 Saccharomyces cerevisiae

Cofactor

Cofactor Comment Organism Structure
ATP 1 mol ATP is hydrolyzed to ADP plus phosphate per mol product formed Saccharomyces cerevisiae
ATP together with Mg2+ Saccharomyces cerevisiae
CTP one third the activity of ATP Saccharomyces cerevisiae
GTP shows almost as much activity as ATP Saccharomyces cerevisiae
ITP shows almost as much activity as ATP Saccharomyces cerevisiae
TTP not Saccharomyces cerevisiae
UTP one third the activity of ATP Saccharomyces cerevisiae