KEGG   PATHWAY: zof00790
Entry
zof00790                    Pathway                                
Name
Folate biosynthesis - Zingiber officinale (ginger)
Class
Metabolism; Metabolism of cofactors and vitamins
Pathway map
zof00790  Folate biosynthesis
zof00790

Module
zof_M00126  Tetrahydrofolate biosynthesis, GTP => THF [PATH:zof00790]
zof_M00880  Molybdenum cofactor biosynthesis, GTP => molybdenum cofactor [PATH:zof00790]
Other DBs
GO: 0046656
Organism
Zingiber officinale (ginger) [GN:zof]
Gene
121967392  [KO:K01930] [EC:6.3.2.17]
121967739  [KO:K01113] [EC:3.1.3.1]
121970686  [KO:K14652] [EC:4.1.99.12 3.5.4.25]
121971840  [KO:K20457] [EC:6.3.2.12]
121972083  [KO:K01495] [EC:3.5.4.16]
121975769  [KO:K14652] [EC:4.1.99.12 3.5.4.25]
121975936  [KO:K01724] [EC:4.2.1.96]
121976883  [KO:K20457] [EC:6.3.2.12]
121977089  [KO:K01495] [EC:3.5.4.16]
121981902  [KO:K03637] [EC:4.6.1.17]
121982127  [KO:K03635] [EC:2.8.1.12]
121985745  [KO:K03637] [EC:4.6.1.17]
121986391  [KO:K18482] [EC:4.1.3.38]
121986808  [KO:K01495] [EC:3.5.4.16]
121988359  [KO:K13998] [EC:1.5.1.3 2.1.1.45]
121989401  [KO:K18482] [EC:4.1.3.38]
121992192  [KO:K01633] [EC:4.1.2.25 5.1.99.8 1.13.11.81]
121992362  [KO:K01724] [EC:4.2.1.96]
121993095  [KO:K15631] [EC:2.8.1.9]
121994979  [KO:K01495] [EC:3.5.4.16]
121997072  [KO:K15631] [EC:2.8.1.9]
121998350  [KO:K18482] [EC:4.1.3.38]
122000256  [KO:K00079] [EC:1.1.1.184 1.1.1.189 1.1.1.197]
122000612  [KO:K01633] [EC:4.1.2.25 5.1.99.8 1.13.11.81]
122000853  [KO:K14652] [EC:4.1.99.12 3.5.4.25]
122003070  [KO:K15376] [EC:2.10.1.1 2.7.7.75]
122003844  [KO:K00079] [EC:1.1.1.184 1.1.1.189 1.1.1.197]
122004904  [KO:K01633] [EC:4.1.2.25 5.1.99.8 1.13.11.81]
122005144  [KO:K14652] [EC:4.1.99.12 3.5.4.25]
122007322  [KO:K15376] [EC:2.10.1.1 2.7.7.75]
122008414  [KO:K13941] [EC:2.7.6.3 2.5.1.15]
122010039  [KO:K01724] [EC:4.2.1.96]
122011019  [KO:K01495] [EC:3.5.4.16]
122012504  [KO:K03635] [EC:2.8.1.12]
122012766  [KO:K14652] [EC:4.1.99.12 3.5.4.25]
122014059  [KO:K01495] [EC:3.5.4.16]
122014339  [KO:K01724] [EC:4.2.1.96]
122014695  [KO:K03635] [EC:2.8.1.12]
122015440  [KO:K01930] [EC:6.3.2.17]
122015476  [KO:K14652] [EC:4.1.99.12 3.5.4.25]
122016031  [KO:K13941] [EC:2.7.6.3 2.5.1.15]
122019870  [KO:K01495] [EC:3.5.4.16]
122020894  [KO:K01930] [EC:6.3.2.17]
122023607  [KO:K01930] [EC:6.3.2.17]
122023626  [KO:K01495] [EC:3.5.4.16]
122027017  [KO:K13950] [EC:2.6.1.85]
122027350  [KO:K03639] [EC:4.1.99.22]
122028585  [KO:K03639] [EC:4.1.99.22]
122029324  [KO:K13950] [EC:2.6.1.85]
122032251  [KO:K03639] [EC:4.1.99.22]
122032634  [KO:K00079] [EC:1.1.1.184 1.1.1.189 1.1.1.197]
122034637  [KO:K03639] [EC:4.1.99.22]
122034977  [KO:K00079] [EC:1.1.1.184 1.1.1.189 1.1.1.197]
122035342  [KO:K01495] [EC:3.5.4.16]
122038154  [KO:K03635] [EC:2.8.1.12]
122038571  [KO:K18482] [EC:4.1.3.38]
122038701  [KO:K13998] [EC:1.5.1.3 2.1.1.45]
122039019  [KO:K01633] [EC:4.1.2.25 5.1.99.8 1.13.11.81]
122040454  [KO:K01307] [EC:3.4.19.9]
122044276  [KO:K01495] [EC:3.5.4.16]
122044975  [KO:K01307] [EC:3.4.19.9]
122047118  [KO:K01930] [EC:6.3.2.17]
122051343  [KO:K01495] [EC:3.5.4.16]
122052605  [KO:K01930] [EC:6.3.2.17]
122052607  [KO:K01930] [EC:6.3.2.17]
122052981  [KO:K01113] [EC:3.1.3.1]
122055748  [KO:K01495] [EC:3.5.4.16]
Compound
C00044  GTP
C00101  Tetrahydrofolate
C00119  5-Phospho-alpha-D-ribose 1-diphosphate
C00156  4-Hydroxybenzoate
C00251  Chorismate
C00266  Glycolaldehyde
C00268  Dihydrobiopterin
C00272  Tetrahydrobiopterin
C00415  Dihydrofolate
C00504  Folate
C00568  4-Aminobenzoate
C00835  Sepiapterin
C00921  Dihydropteroate
C01217  5,6,7,8-Tetrahydromethanopterin
C01300  6-(Hydroxymethyl)-7,8-dihydropterin
C01304  2,5-Diamino-6-(5-phospho-D-ribosylamino)pyrimidin-4(3H)-one
C02587  Pyrimidodiazepine
C02953  7,8-Dihydrobiopterin
C03541  THF-polyglutamate
C03684  6-Pyruvoyltetrahydropterin
C04244  6-Lactoyl-5,6,7,8-tetrahydropterin
C04807  6-Hydroxymethyl-7,8-dihydropterin diphosphate
C04874  7,8-Dihydroneopterin
C04895  7,8-Dihydroneopterin 3'-triphosphate
C05922  Formamidopyrimidine nucleoside triphosphate
C05923  2,5-Diaminopyrimidine nucleoside triphosphate
C05924  Molybdopterin
C05925  Dihydroneopterin phosphate
C05926  Neopterin
C05927  7,8-Dihydromethanopterin
C06148  2,5-Diamino-6-(5'-triphosphoryl-3',4'-trihydroxy-2'-oxopentyl)-amino-4-oxopyrimidine
C06313  Biopterin
C09332  THF-L-glutamate
C11355  4-Amino-4-deoxychorismate
C15522  4a-Hydroxytetrahydrobiopterin
C15996  7-Cyano-7-carbaguanine
C16675  7-Aminomethyl-7-carbaguanine
C18237  Molybdoenzyme molybdenum cofactor
C18239  Precursor Z
C18802  Tetrahydrosarcinapterin
C19848  Adenylated molybdopterin
C19871  Guanylyl molybdenum cofactor
C20239  6-Carboxy-5,6,7,8-tetrahydropterin
C20248  7-Carboxy-7-carbaguanine
C20264  L-threo-Tetrahydrobiopterin
C20559  4-(beta-D-Ribofuranosyl)aniline 5'-phosphate
C20562  N-[(7,8-Dihydropterin-6-yl)methyl]-4-(beta-D-ribofuranosyl)aniline 5'-phosphate
C20566  7,8-Dihydroneopterin 2'-phosphate
C20567  7,8-Dihydroneopterin 2',3'-cyclic phosphate
C21007  5,6,7,8-Tetrahydromonapterin
C21008  7,8-Dihydromonapterin
C21065  7,8-Dihydroxanthopterin
C21094  7,8-Dihydromonapterin 3'-triphosphate
C21107  4-(beta-D-Ribofuranosyl)phenol 5'-phosphate
C21310  (8S)-3',8-Cyclo-7,8-dihydroguanosine 5'-triphosphate
C21485  Cytidylyl molybdenum cofactor
C21486  Thio-molybdenum cofactor
C21640  6-(1'-Hydroxy-2'-oxopropyl)-tetrahydropterin
Reference
  Authors
Nishizuka Y, Seyama Y, Ikai A, Ishimura Y, Kawaguchi A (eds).
  Title
[Cellular Functions and Metabolic Maps] (In Japanese)
  Journal
Tokyo Kagaku Dojin (1997)
Reference
  Authors
Schwarz G, Mendel RR, Ribbe MW
  Title
Molybdenum cofactors, enzymes and pathways.
  Journal
Nature 460:839-47 (2009)
DOI:10.1038/nature08302
Reference
  Authors
Hanzelmann P, Schindelin H
  Title
Binding of 5'-GTP to the C-terminal FeS cluster of the radical S-adenosylmethionine enzyme MoaA provides insights into its mechanism.
  Journal
Proc Natl Acad Sci U S A 103:6829-34 (2006)
DOI:10.1073/pnas.0510711103
Reference
  Authors
Daniels JN, Wuebbens MM, Rajagopalan KV, Schindelin H
  Title
Crystal structure of a molybdopterin synthase-precursor Z complex: insight into its sulfur transfer mechanism and its role in molybdenum cofactor deficiency.
  Journal
Biochemistry 47:615-26 (2008)
DOI:10.1021/bi701734g
Reference
  Authors
Wuebbens MM, Rajagopalan KV
  Title
Mechanistic and mutational studies of Escherichia coli molybdopterin synthase clarify the final step of molybdopterin biosynthesis.
  Journal
J Biol Chem 278:14523-32 (2003)
DOI:10.1074/jbc.M300453200
Reference
  Authors
Werner ER, Blau N, Thony B
  Title
Tetrahydrobiopterin: biochemistry and pathophysiology.
  Journal
Biochem J 438:397-414 (2011)
DOI:10.1042/BJ20110293
Reference
  Authors
Iino T, Tabata M, Takikawa S, Sawada H, Shintaku H, Ishikura S, Hara A
  Title
Tetrahydrobiopterin is synthesized from 6-pyruvoyl-tetrahydropterin by the human aldo-keto reductase AKR1 family members.
  Journal
Arch Biochem Biophys 416:180-7 (2003)
DOI:10.1016/S0003-9861(03)00295-9
Reference
PMID:1902669
  Authors
Park YS, Heizmann CW, Wermuth B, Levine RA, Steinerstauch P, Guzman J, Blau N
  Title
Human carbonyl and aldose reductases: new catalytic functions in tetrahydrobiopterin biosynthesis.
  Journal
Biochem Biophys Res Commun 175:738-44 (1991)
DOI:10.1016/0006-291X(91)91628-P
Related
pathway
zof00230  Purine metabolism
zof00400  Phenylalanine, tyrosine and tryptophan biosynthesis
zof00670  One carbon pool by folate
KO pathway
ko00790   

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