3.5.2.15: cyanuric acid amidohydrolase
This is an abbreviated version!
For detailed information about cyanuric acid amidohydrolase, go to the full flat file.
Word Map on EC 3.5.2.15
-
3.5.2.15
-
biuret
-
agriculture
-
barbituric
-
thermoacetica
-
moorella
-
ring-opening
-
swimming
-
hydrolases
-
disinfect
-
adp
-
herbicide
-
melamine
-
environmental protection
-
ammeline
-
atrazine
-
rhodococcus
-
ser-lys
-
dyad
-
chlorine
-
acidovorax
-
citrulli
-
aminohydrolase
-
acid-degrading
-
allophanate
-
tight-binding
-
enterobacter
-
caulinodans
-
hypochlorite
-
prebiotic
-
azorhizobium
- 3.5.2.15
- biuret
- agriculture
-
barbituric
- thermoacetica
-
moorella
-
ring-opening
-
swimming
- hydrolases
-
disinfect
- adp
-
herbicide
- melamine
- environmental protection
- ammeline
- atrazine
-
rhodococcus
- ser-lys
-
dyad
-
chlorine
-
acidovorax
- citrulli
-
aminohydrolase
-
acid-degrading
- allophanate
-
tight-binding
- enterobacter
- caulinodans
-
hypochlorite
-
prebiotic
-
azorhizobium
Reaction
Synonyms
amidase, cyanurate, AtzD, CAH, cyanurate amidase, cyanuric acid hydrolase, s-triazine ring-cleavage enzyme, TrzD, trzD gene product
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Substrates Products
Substrates Products on EC 3.5.2.15 - cyanuric acid amidohydrolase
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REACTION DIAGRAM
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
cyanuric acid + H2O
biuret + CO2
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
Gordonia rubripertincta DSM 10347 / NRRLB-15444R
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
Gordonia rubripertincta DSM 10347 / NRRLB-15444R
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
Gordonia rubripertincta DSM 10347 / NRRLB-15444R
-
2,4,6-trihydroxy-s-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
Hormodendrum sp.
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-s-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
heterocyclic ring cleavage
-
-
?
cyanuric acid + H2O
biuret + CO2
-
first enzyme of degradative pathway of cyanuric acid
-
-
?
cyanuric acid + H2O
biuret + CO2
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
cyanuric acid + H2O
biuret + CO2
-
herterocyclic ring cleavage
-
-
?
cyanuric acid + H2O
biuret + CO2
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-s-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-s-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-s-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-s-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-s-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
Penicillium spp.
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-s-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
heterocyclic ring cleavage
-
-
?
cyanuric acid + H2O
biuret + CO2
-
fourth step in the six-step pathway for metabolism of melamine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
first enzyme of degradative pathway of cyanuric acid
-
-
?
cyanuric acid + H2O
biuret + CO2
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
cyanuric acid + H2O
biuret + CO2
-
herterocyclic ring cleavage
-
-
?
cyanuric acid + H2O
biuret + CO2
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
cyanuric acid + H2O
biuret + CO2
-
2,4,6-trihydroxy-1,3,5-triazine
-
-
?
cyanuric acid + H2O
biuret + CO2
-
1,3,5-triazine-2,4,6(1H,3H,5H)-trione
-
-
?
carboxybiuret
-
-
product spontaneously decarboxylates to give biuret and CO2. Therefore cyanuric acid hydrolase and barbiturase catalyze completely analogous reactions
-
?
cyanuric acid + H2O
carboxybiuret
-
-
product spontaneously decarboxylates to give biuret and CO2. Therefore cyanuric acid hydrolase and barbiturase catalyze completely analogous reactions
-
?
cyanuric acid + H2O
carboxybiuret
-
-
product spontaneously decarboxylates to give biuret and CO2. Therefore cyanuric acid hydrolase and barbiturase catalyze completely analogous reactions
-
?
cyanuric acid + H2O
carboxybiuret
-
product spontaneously decarboxylates to give biuret and CO2. Therefore cyanuric acid hydrolase and barbiturase catalyze completely analogous reactions
-
?
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
Gordonia rubripertincta DSM 10347 / NRRLB-15444R
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
Gordonia rubripertincta DSM 10347 / NRRLB-15444R
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
strain A, no activity with ammeline, 2,4-diamino-6-hydroxy-s-triazine, ammelide, 2-amino-4,6-dihydroxy-s-triazine, uracil, 2,4-dihydroxypyrimidine, 5,6-dihydrouracil, cytosine, 4-amino-2-hydroxypyrimidine, 2,4,5-trihydroxypyrimidine and barbituric acid, 2,4,6-trihydroxypyrimidine
-
-
?
additional information
?
-
-
strain A, high substrate specificity, no activity with any other s-triazine or hydroxypyrimidine compound
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
one step in the six-step pathway for metabolism of melamine
-
-
?
additional information
?
-
hypothetical reaction mechanism consistent with a Ser85 nucleophile. Lys42 is a general base, activating Ser85 and promoting formation of a tetrahedral intermediate between Ser85 and the closest substrate carbonyl carbon, this then resolves into the acyl:enzyme intermediate following ring opening. Thereafter, a solvent water molecule is required to hydrolyse the acyl intermediate and regenerate the serine, liberating carboxybiuret
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?
additional information
?
-
-
one step in the six-step pathway for metabolism of melamine
-
-
?
additional information
?
-
-
strain A, no activity with ammeline, 2,4-diamino-6-hydroxy-s-triazine, ammelide, 2-amino-4,6-dihydroxy-s-triazine, uracil, 2,4-dihydroxypyrimidine, 5,6-dihydrouracil, cytosine, 4-amino-2-hydroxypyrimidine, 2,4,5-trihydroxypyrimidine and barbituric acid, 2,4,6-trihydroxypyrimidine
-
-
?
additional information
?
-
-
strain A, high substrate specificity, no activity with any other s-triazine or hydroxypyrimidine compound
-
-
?
additional information
?
-
-
involved in a pathway by which herbicides or pesticides based on the symmetrical triazine ring, s-triazine, including atrazine, 2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine, are degraded in bacteria
-
-
?
additional information
?
-
-
involved in metabolism of s-triazine ring structure, component of several important herbicides, including atrazine
-
-
?