KEGG   MODULE: M00116
Entry
M00116            Pathway   Module                                 
Name
Menaquinone biosynthesis, chorismate (+ polyprenyl-PP) => menaquinol
Definition
K02552 K02551 K08680 K02549 K01911 K01661 K19222 K02548 K03183
Diagram
M00116

Orthology
K02552  
isochorismate synthase [EC:5.4.4.2] [RN:R01717]
K02551  
2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase [EC:2.2.1.9] [RN:R08165]
K08680  
2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase [EC:4.2.99.20] [RN:R08166]
K02549  
O-succinylbenzoate-CoA synthase [EC:4.2.1.113] [RN:R04031]
K01911  
O-succinylbenzoic acid--CoA ligase [EC:6.2.1.26] [RN:R04030]
K01661  
naphthoate synthase [EC:4.1.3.36] [RN:R07263]
K19222  
1,4-dihydroxy-2-naphthoyl-CoA hydrolase [EC:3.1.2.28] [RN:R07262]
K02548  
1,4-dihydroxy-2-naphthoate polyprenyltransferase [EC:2.5.1.74] [RN:R10757]
K03183  
demethylmenaquinone methyltransferase [EC:2.1.1.163] [RN:R09736]
Class
Pathway modules; Metabolism of cofactors and vitamins; Cofactor and vitamin metabolism
Pathway
map00130  Ubiquinone and other terpenoid-quinone biosynthesis
map01240  Biosynthesis of cofactors
map01100  Metabolic pathways
map01110  Biosynthesis of secondary metabolites
Reaction
Compound
C00251  Chorismate
C00885  Isochorismate
C16519  2-Succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate
C05817  (1R,6R)-6-Hydroxy-2-succinylcyclohexa-2,4-diene-1-carboxylate
C02730  2-Succinylbenzoate
C03160  2-Succinylbenzoyl-CoA
C15547  1,4-Dihydroxy-2-naphthoyl-CoA
C03657  1,4-Dihydroxy-2-naphthoate
C05847  all-trans-Polyprenyl diphosphate
C19847  Demethylmenaquinol
C05819  Menaquinol
Reference
  Authors
Chen M, Ma X, Chen X, Jiang M, Song H, Guo Z
  Title
Identification of a hotdog fold thioesterase involved in the biosynthesis of menaquinone in Escherichia coli.
  Journal
J Bacteriol 195:2768-75 (2013)
DOI:10.1128/JB.00141-13
Reference
  Authors
Joshi S, Fedoseyenko D, Mahanta N, Manion H, Naseem S, Dairi T, Begley TP
  Title
Novel enzymology in futalosine-dependent menaquinone biosynthesis.
  Journal
Curr Opin Chem Biol 47:134-141 (2018)
DOI:10.1016/j.cbpa.2018.09.015
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