Selected compound(s)
Each orphan metabolite is emphasized in bold.
Click [Fig] on the left hand, and the image of the reaction is shown.
[Suggested reactions |
Reported reactions]
Suggested reactions
- [Fig] 1.3.4.- : Uracil + 1,4-Dithiothreitol = 2,4(1H,3H)-Pyrimidinedione, dihydro- + Oxidized dithiothreitol
- [Fig] 1.3.4.- : Uracil + 1,4-Dithiothreitol = 2,4(1H,3H)-Pyrimidinedione, dihydro- + Oxidized dithiothreitol
- [Fig] 1.3.5.- : Uracil + CoQH2 = 2,4(1H,3H)-Pyrimidinedione, dihydro- + CoQ
- [Fig] 1.3.5.- : Uracil + CoQH2 = 2,4(1H,3H)-Pyrimidinedione, dihydro- + CoQ
- [Fig] 1.3.99.- : 2,4(1H,3H)-Pyrimidinedione, dihydro- + FAD = Uracil + FADH2
- [Fig] 1.3.99.- : 2,4(1H,3H)-Pyrimidinedione, dihydro- + FAD = Uracil + FADH2
- [Fig] 1.3.99.- : 2,4(1H,3H)-Pyrimidinedione, dihydro- + Coenzyme F420 = Uracil + Reduced coenzyme F420
- [Fig] 1.3.99.- : 2,4(1H,3H)-Pyrimidinedione, dihydro- + Coenzyme F420 = Uracil + Reduced coenzyme F420
- [Fig] 1.14.11.- : Uracil + O2 + 2-Ketoglutaric acid = Barbiturate + CO2 + Butanedionic acid
- [Fig] 1.14.13.- : Barbiturate + H2O + NAD+ = Uracil + NADH + O2 + H+
- [Fig] 1.14.13.- : Barbiturate + H2O + NADP+ = Uracil + NADPH + O2 + H+
- [Fig] 1.14.16.- : Barbiturate + 6,7-Dihydrobiopterin + H2O = Uracil + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.17.- : Uracil + Vitamin C + O2 = Barbiturate + Dehydroascorbate + H2O
- [Fig] 2.1.2.- : Uracil 5-carboxylate + THF = Uracil + 10-Formyl-THF
- [Fig] 2.5.1.- : 3-(Uracil-1-yl)-L-alanine + Ammonia = 2,3-Diaminopropanoate + Uracil
- [Fig] 3.2.1.- : Pseudouridine 5'-phosphate + H2O = D-Ribose 5-phosphate + Uracil
- [Fig] 3.5.4.- : Cytosine + H2O = Uracil + Ammonia
- [Fig] 3.5.99.- : UDP + H2O = D-Ribose 5-diphosphate + Uracil
- [Fig] 3.5.99.- : Uridine + H2O = D-Ribose + Uracil
- [Fig] 3.7.1.- : Uracil 5-carboxylate + H2O = Uracil + Formate
- [Fig] 4.1.1.- : Uracil + CO2 = Uracil 5-carboxylate
- [Fig] 6.3.4.- : Uracil + ATP + Ammonia = Cytosine + ADP + Orthophosphate
- [Fig] 6.3.4.- : Uracil + ATP + Ammonia = Cytosine + Orthophosphate
- [Fig] 6.3.4.- : Uracil + ATP + Ammonia = Cytosine + Diphosphate
- [Fig] 6.3.4.- : Uracil + ATP + Ammonia = Cytosine + Diphosphate + 5'-AMP
- [Fig] 6.3.4.- : D-Ribose + Uracil + ATP = Uridine + ADP + Orthophosphate
- [Fig] 6.3.4.- : D-Ribose + Uracil + ATP = Uridine + Diphosphate + 5'-AMP
- [Fig] 6.3.4.- : D-Ribose 5-diphosphate + Uracil + ATP = UDP + ADP + Orthophosphate
- [Fig] 6.3.4.- : D-Ribose 5-diphosphate + Uracil + ATP = UDP + Diphosphate + 5'-AMP
- [Fig] 6.4.1.- : Uracil + ATP + Acid carbonate = Uracil 5-carboxylate + ADP + Orthophosphate
- [Fig] 6.4.1.- : D-Ribose 5-phosphate + Uracil + ATP = Pseudouridine 5'-phosphate + ADP + Orthophosphate
- [Fig] 6.4.1.- : Uracil 5-carboxylate + ADP + Orthophosphate = Uracil + Formate + ATP
Reported reactions
- [Fig] EC 3.2.2.3 : Uridine + H2O = Uracil + D-Ribose
- [Fig] EC 4.1.1.66 : Uracil 5-carboxylate = Uracil + CO2
- [Fig] EC 3.5.4.1 : Cytosine + H2O = Uracil + Ammonia
- [Fig] EC 1.3.3.7 : 2,4(1H,3H)-Pyrimidinedione, dihydro- + O2 = Uracil + H2O2
- [Fig] EC 1.1.99.19 : Uracil + Acceptor = Barbiturate + Reduced acceptor
- [Fig] EC 1.3.1.1 : 2,4(1H,3H)-Pyrimidinedione, dihydro- + NAD+ = Uracil + NADH + H+
- [Fig] EC 1.3.1.2 : 2,4(1H,3H)-Pyrimidinedione, dihydro- + NADP+ = Uracil + NADPH + H+
- [Fig] EC 2.5.1.53 : O-Acetyl-L-serine + Uracil = 3-(Uracil-1-yl)-L-alanine + Acetate
- [Fig] EC 4.2.1.70 : Uracil + D-Ribose 5-phosphate = Pseudouridine 5'-phosphate + H2O
- [Fig] EC 2.4.2.3 : Uridine + Orthophosphate = Uracil + Ribose 1-phosphate
- [Fig] EC 2.4.2.1 : 2'-Deoxyuridine + Orthophosphate = Uracil + 2-Deoxy-D-ribose 1-phosphate
- [Fig] EC 2.4.2.4 : 2'-Deoxyuridine + Orthophosphate = Uracil + 2-Deoxy-D-ribose 1-phosphate
- [Fig] EC 2.4.2.23 : 2'-Deoxyuridine + Orthophosphate = Uracil + Deoxy-ribose 1-phosphate
- [Fig] EC 1.14.11.10 : 2'-Deoxyuridine + 2-Ketoglutaric acid + O2 = Deoxyribonolactone + Uracil + Butanedionic acid + CO2
- [Fig] EC 2.4.2.9 : UMP + Diphosphate = Uracil + 5-Phosphoribosyl diphosphate
GREP v1.0.2 http://bisscat.org/GREP/
Developed by Masaaki Kotera (2008), Department of Biochemistry, Trinity College Dublin.
Science Foundation of Ireland is gratefully acknowledged.