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Literature summary for 3.5.4.12 extracted from

  • Keefe, R.G.; Maley, G.F.; Saxl, R.L.; Maley, F.
    A T4-phage deoxycytidylate deaminase mutant that no longer requires deoxycytidine 5'-triphosphate for activation (2000), J. Biol. Chem., 275, 12598-12602.
    View publication on PubMed

Activating Compound

Activating Compound Comment Organism Structure
5-hydroxymethyl-dCTP natural positive allosteric effector, enzyme is much more effectively regulated by its natural effector, 5-hydroxymethyl-dCTP, than by dCTP, binding of 5-hydroxymethyl-dCTP is much more pH dependent than dCTP Tequatrovirus T4
5-hydroxymethyl-dCTP natural positive allosteric effector, enzyme is much more effectively regulated by its natural effector, 5-hydroxymethyl-dCTP, than by dCTP, binding of 5-hydroxymethyl-dCTP is much more pH dependent than dCTP Escherichia phage T2
5-hydroxymethyl-dCTP natural positive allosteric effector, enzyme is much more effectively regulated by its natural effector, 5-hydroxymethyl-dCTP, than by dCTP, binding of 5-hydroxymethyl-dCTP is much more pH dependent than dCTP Enterobacteria phage T6
5-hydroxymethyl-dCTP natural activator, required for activity Tequatrovirus T4
dCTP required for activity Tequatrovirus T4
dCTP positive allosteric effector Tequatrovirus T4
dCTP positive allosteric effector Escherichia phage T2
dCTP positive allosteric effector Enterobacteria phage T6
dCTP hexameric form of enzyme is activated by dCTP, while the dimer is not Tequatrovirus T4
dCTP wild-type, dCTP required for activity, no activity in absence of dCTP and Mg2+ Tequatrovirus T4
dCTP severalfold activation, activation requires presence of Mg2+ Tequatrovirus T4
dCTP severalfold activation, activation requires presence of Mg2+ Escherichia phage T2
dCTP severalfold activation, activation requires presence of Mg2+ Enterobacteria phage T6
dCTP mutants R115E and R115Q: dCTP not required. R115Q: slight, 30-40% activation by 0.02 mM dCTP Tequatrovirus T4
additional information the phage dCMP deaminase expression is increased upon infection of Escherichia coli Tequatrovirus T4

Cloned(Commentary)

Cloned (Comment) Organism
expression of wild-type and mutant enzymes in Escherichia coli Tequatrovirus T4

Protein Variants

Protein Variants Comment Organism
F112A molecular weight analysis using HPLC gel filtration in the presence of SDS and dCTP: wild-type is a hexamer, F112A varies from hexamer to dimer Tequatrovirus T4
F112A site-directed mutagenesis, the mutant enzyme shows reduced turnover and activity compared to the wild-type enzyme Tequatrovirus T4
R115E mutant enzyme active in the absence of dCTP and Mg2+, little if any activation by dCTP, possessing turnover number or kcat that is about 15% that of wild-type enzyme, specific activity about 40-50% of wild-type enzyme. Molecular weight analysis using HPLC gel filtration in the presence of SDS and dCTP: wild-type is a hexamer, R115E a dimer Tequatrovirus T4
R115E site-directed mutagenesis, the mutant enzyme shows reduced turnover and activity compared to the wild-type enzyme, but no longer requires deoxycytidine 5-triphosphate for activation in contrast to the wild-type enzyme Tequatrovirus T4
R115Q mutant enzyme active in the absence of dCTP and Mg2+, possessing turnover number or kcat that is about 15% that of wild-type enzyme, specific activity about 40-50% of wild-type enzyme. Molecular weight analysis using HPLC size gel filtration in the presence of SDS and dCTP: wild-type is a hexamer, R115Q varies from hexamer to dimer Tequatrovirus T4
R115Q site-directed mutagenesis, the mutant enzyme shows reduced turnover and activity compared to the wild-type enzyme, but no longer requires deoxycytidine 5-triphosphate for activation in contrast to the wild-type enzyme Tequatrovirus T4

General Stability

General Stability Organism
2-mercaptoethanol stabilizes Tequatrovirus T4
2-mercaptoethanol stabilizes Escherichia phage T2
EDTA: denaturation, EDTA removes the two resident Zn2+ atoms /subunit Tequatrovirus T4
guanidine-HCl, 6 M, denaturation, complete restoration of activity on removal of denaturant by dilution or dialysis Tequatrovirus T4

Inhibitors

Inhibitors Comment Organism Structure
dTTP allosteric inhibitor Enterobacteria phage T6
dTTP allosteric inhibitor Escherichia phage T2
dTTP allosteric inhibitor; wild-type, 0.1 mM dTTP: 20% inhibition, mutants R115E and R115Q: 0.1 mM dTTP: no inhibition. 0.3 mM dTTP: wild-type 90% inhibition, mutants R115E and R115Q: 30% inhibition Tequatrovirus T4
EDTA
-
Tequatrovirus T4

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
additional information
-
additional information
-
Escherichia phage T2
additional information
-
additional information kinetic analysis, data and characterization of wild-type and mutants R115E, R115Q and F112A Tequatrovirus T4
0.021
-
dCMP wild-type, presence of dCTP and Mg2+ Tequatrovirus T4
0.021
-
dCMP recombinant wild-type enzyme, pH 8.0, 30°C Tequatrovirus T4
0.127
-
dCMP R115Q, absence of dCTP Tequatrovirus T4
0.127
-
dCMP recombinant mutant R115Q, pH 8.0, 30°C Tequatrovirus T4
0.137
-
dCMP R115E, absence of dCTP Tequatrovirus T4
0.137
-
dCMP recombinant mutant R115E, pH 8.0, 30°C Tequatrovirus T4

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+
-
Tequatrovirus T4
Mg2+ required for activation by dCTP and for inhibition by dTTP Tequatrovirus T4
Mg2+ required for activation by dCTP and for inhibition by dTTP Escherichia phage T2
Mg2+ required for activation by dCTP and for inhibition by dTTP Enterobacteria phage T6
Zn2+ two resident Zn2+ atoms /subunit Tequatrovirus T4

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
21200
-
6 * 21200, wild-type, particularly in the presence of dCTP: hexamer, mutants R115Q and F112A varies from hexamers to dimers or something in between depending on protein concentration, HPLC gel filtration in the presence of SDS Tequatrovirus T4
21200
-
2 * 21200, mutant R115E: dimer, mutants R115Q and F112A varies from hexamers to dimers or something in between depending on protein concentration, HPLC gel filtration in the presence of SDS Tequatrovirus T4
38200 113000 recombinant mutant F112A, gel filtration, dependent on protein concentration, in presence and absence of fdCTP Tequatrovirus T4
39800 118000 recombinant mutant R115Q, gel filtration, dependent on protein concentration, in presence and absence of fdCTP Tequatrovirus T4
41600 45400 recombinant mutant R115E, gel filtration, dependent on protein concentration, in presence and absence of fdCTP Tequatrovirus T4
44300
-
R115E, HPLC gel filtration Tequatrovirus T4
110000 122000 recombinant wild-type enzyme, gel filtration, dependent on protein concentration, in presence and absence of fdCTP Tequatrovirus T4
111900
-
F112A, HPLC gel filtration Tequatrovirus T4
124500
-
R115Q, HPLC gel filtration Tequatrovirus T4
127000
-
wild-type, HPLC gel filtration Tequatrovirus T4

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
dCMP + H2O Tequatrovirus T4
-
dUMP + NH3
-
?
dCMP + H2O Escherichia phage T2
-
dUMP + NH3
-
?

Organism

Organism UniProt Comment Textmining
Enterobacteria phage T6
-
T2-, T4-, and T6-phage induced enzyme in Escherichia coli
-
Escherichia phage T2
-
T2-, T4-, and T6-phage induced enzyme in Escherichia coli
-
Tequatrovirus T4
-
-
-
Tequatrovirus T4
-
T2-, T4-, and T6-phage induced enzyme in Escherichia coli
-
Tequatrovirus T4
-
wild-type and R115E and R115Q, mutant enzymes that no longer requires dCTP for activation, and mutant F112A
-
Tequatrovirus T4
-
T4-phage infected Escherichia coli
-

Purification (Commentary)

Purification (Comment) Organism
recombinant wild-type and mutant enzymes from Escherichia coli Tequatrovirus T4
wild-type and mutants R115E, R115Q and F112A Tequatrovirus T4

Reaction

Reaction Comment Organism Reaction ID
dCMP + H2O = dUMP + NH3 regulation, allosteric end-product regulation Tequatrovirus T4
dCMP + H2O = dUMP + NH3 regulation, allosteric end-product regulation Escherichia phage T2
dCMP + H2O = dUMP + NH3 regulation, allosteric end-product regulation Enterobacteria phage T6
dCMP + H2O = dUMP + NH3 highly regulated allosteric enzyme Tequatrovirus T4
dCMP + H2O = dUMP + NH3 highly regulated allosteric enzyme Escherichia phage T2
dCMP + H2O = dUMP + NH3 highly regulated allosteric enzyme Enterobacteria phage T6

Renatured (Commentary)

Renatured (Comment) Organism
after denaturation with EDTA, mutants R115E and R115Q restored 54% and 60% of original activities, wild-type enzyme only marginally restored Tequatrovirus T4
after treatment with guanidine-HCl, 6 M, complete reactivation on removal of denaturant by dilution or dialysis Tequatrovirus T4

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
additional information
-
mutants R115E and R115Q possessing specific activity about 40-50% of wild-type enzyme Tequatrovirus T4
90 100 mutant R115E Tequatrovirus T4
121
-
mutant R115Q Tequatrovirus T4
220
-
wild-type Tequatrovirus T4

Storage Stability

Storage Stability Organism
-40°C, solid ammonium sulfate to 80% saturation, stable for longer periods of storage Tequatrovirus T4
0-4°C, 0.1 M 2-mercaptoethanol, stable for extended periods Tequatrovirus T4

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
dCMP + H2O
-
Tequatrovirus T4 dUMP + NH3
-
?
dCMP + H2O
-
Escherichia phage T2 dUMP + NH3
-
?
dCMP + H2O
-
Enterobacteria phage T6 dUMP + NH3
-
?

Subunits

Subunits Comment Organism
dimer 2 * 21200, mutant R115E: dimer, mutants R115Q and F112A varies from hexamers to dimers or something in between depending on protein concentration, HPLC gel filtration in the presence of SDS Tequatrovirus T4
dimer mutants R115Q and R115E, mutant F112A changes between dimeric and hexameric forms Tequatrovirus T4
hexamer 6 identical subunits Tequatrovirus T4
hexamer 6 identical subunits Escherichia phage T2
hexamer 6 identical subunits Enterobacteria phage T6
hexamer 6 * 21200, wild-type, particularly in the presence of dCTP: hexamer, mutants R115Q and F112A varies from hexamers to dimers or something in between depending on protein concentration, HPLC gel filtration in the presence of SDS Tequatrovirus T4
hexamer wild-type enzyme, mutant F112A changes between dimeric and hexameric forms Tequatrovirus T4
More hexameric form of enzyme is activated by dCTP, while the dimer is not Tequatrovirus T4

Synonyms

Synonyms Comment Organism
dCMP deaminase
-
Tequatrovirus T4
deoxycytidylate deaminase
-
Tequatrovirus T4

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
30
-
assay at Tequatrovirus T4

Turnover Number [1/s]

Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
additional information
-
additional information mutants R115E and R115Q possessing turnover number or kcat that is about 15% that of wild-type enzyme Tequatrovirus T4
69
-
dCMP R115E Tequatrovirus T4
69
-
dCMP mutant R115E, pH 8.0, 30°C Tequatrovirus T4
85
-
dCMP R115Q dimer Tequatrovirus T4
85
-
dCMP mutant R115Q, pH 8.0, 30°C Tequatrovirus T4
255
-
dCMP R115Q hexamer Tequatrovirus T4
466
-
dCMP wild-type Tequatrovirus T4
466
-
dCMP wild-type enzyme, pH 8.0, 30°C Tequatrovirus T4

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
8
-
assay at Tequatrovirus T4
8
-
assay at Escherichia phage T2