KEGG   PATHWAY: pvd00350
Entry
pvd00350                    Pathway                                
Name
Tyrosine metabolism - Pseudomonas viridiflava
Class
Metabolism; Amino acid metabolism
Pathway map
pvd00350  Tyrosine metabolism
pvd00350

Module
pvd_M00044  Tyrosine degradation, tyrosine => homogentisate [PATH:pvd00350]
Other DBs
GO: 0006570
Organism
Pseudomonas viridiflava [GN:pvd]
Gene
CFBP1590_0348  davD; Glutarate-semialdehyde dehydrogenase DavD [KO:K00135] [EC:1.2.1.16 1.2.1.79 1.2.1.20]
CFBP1590_0408  davD; Glutarate-semialdehyde dehydrogenase DavD [KO:K00135] [EC:1.2.1.16 1.2.1.79 1.2.1.20]
CFBP1590_0475  [KO:K00274] [EC:1.4.3.4]
CFBP1590__1141  hisC; Histidinol-phosphate aminotransferase [KO:K00817] [EC:2.6.1.9]
CFBP1590__2021  aspC; Aspartate aminotransferase [KO:K00832] [EC:2.6.1.57]
CFBP1590__2541  araE; Alpha-ketoglutaric semialdehyde dehydrogenase [KO:K00135] [EC:1.2.1.16 1.2.1.79 1.2.1.20]
CFBP1590__2749  [KO:K00274] [EC:1.4.3.4]
CFBP1590__3430  fah; Fumarylacetoacetase [KO:K01555] [EC:3.7.1.2]
CFBP1590__3431  hmgA; Homogentisate 1,2-dioxygenase [KO:K00451] [EC:1.13.11.5]
CFBP1590__3433  hpd; 4-hydroxyphenylpyruvate dioxygenase [KO:K00457] [EC:1.13.11.27]
CFBP1590__3434  maiA; Maleylacetoacetate isomerase [KO:K01800] [EC:5.2.1.2]
CFBP1590__3569  phhC; Aromatic-amino-acid aminotransferase [KO:K00813] [EC:2.6.1.1]
CFBP1590__4021  frmA; S-(hydroxymethyl)glutathione dehydrogenase [KO:K00121] [EC:1.1.1.284 1.1.1.1]
CFBP1590__5153  tyrB; Aromatic-amino-acid aminotransferase [KO:K00832] [EC:2.6.1.57]
Compound
C00022  Pyruvate
C00042  Succinate
C00082  L-Tyrosine
C00122  Fumarate
C00146  Phenol
C00164  Acetoacetate
C00232  Succinate semialdehyde
C00355  3,4-Dihydroxy-L-phenylalanine
C00483  Tyramine
C00530  Hydroquinone
C00544  Homogentisate
C00547  L-Noradrenaline
C00628  2,5-Dihydroxybenzoate
C00642  4-Hydroxyphenylacetate
C00788  L-Adrenaline
C00811  4-Coumarate
C00822  Dopaquinone
C01036  4-Maleylacetoacetate
C01060  3,5-Diiodo-L-tyrosine
C01061  4-Fumarylacetoacetate
C01161  3,4-Dihydroxyphenylacetate
C01179  3-(4-Hydroxyphenyl)pyruvate
C01384  Maleic acid
C01693  L-Dopachrome
C01829  Thyroxine
C01850  Rosmarinate
C02167  Maleylpyruvate
C02442  N-Methyltyramine
C02465  Triiodothyronine
C02514  3-Fumarylpyruvate
C02515  3-Iodo-L-tyrosine
C03063  2-Oxohept-3-enedioate
C03077  4-Chlorophenylacetate
C03758  Dopamine
C03765  4-Hydroxyphenylacetaldehyde
C03964  (R)-3-(4-Hydroxyphenyl)lactate
C04043  3,4-Dihydroxyphenylacetaldehyde
C04045  3-(3,4-Dihydroxyphenyl)pyruvate
C04052  5-Carboxy-2-oxohept-3-enedioate
C04185  5,6-Dihydroxyindole-2-carboxylate
C04186  5-Carboxymethyl-2-hydroxymuconate
C04368  3-Amino-3-(4-hydroxyphenyl)propanoate
C04642  2-Hydroxy-5-carboxymethylmuconate semialdehyde
C04796  4-(L-Alanin-3-yl)-2-hydroxy-cis,cis-muconate 6-semialdehyde
C04797  5-(L-Alanin-3-yl)-2-hydroxy-cis,cis-muconate 6-semialdehyde
C05338  4-Hydroxyphenylacetyl-CoA
C05350  2-Hydroxy-3-(4-hydroxyphenyl)propenoate
C05576  3,4-Dihydroxyphenylethyleneglycol
C05577  3,4-Dihydroxymandelaldehyde
C05578  5,6-Dihydroxyindole
C05579  Indole-5,6-quinone
C05580  3,4-Dihydroxymandelate
C05581  3-Methoxy-4-hydroxyphenylacetaldehyde
C05582  Homovanillate
C05583  3-Methoxy-4-hydroxyphenylglycolaldehyde
C05584  3-Methoxy-4-hydroxymandelate
C05585  Gentisate aldehyde
C05587  3-Methoxytyramine
C05588  L-Metanephrine
C05589  L-Normetanephrine
C05593  3-Hydroxyphenylacetate
C05594  3-Methoxy-4-hydroxyphenylethyleneglycol
C05595  4-Hydroxyphenylacetylglutamic acid
C05596  p-Hydroxyphenylacetylglycine
C05600  2-Hydroxyhepta-2,4-dienedioate
C05604  2-Carboxy-2,3-dihydro-5,6-dihydroxyindole
C06044  4-Hydroxyphenylethanol
C06046  Salidroside
C06047  Stizolobate
C06048  Stizolobinate
C06199  Hordenine
C06201  2,4-Dihydroxyhept-2-enedioate
C10447  3,4-Dihydroxyphenylpropanoate
C17935  Cysteinyldopa
C17936  Phaeomelanin
C17937  Eumelanin
C17938  5,6-Indolequinone-2-carboxylic acid
C22038  (R)-3-(3,4-Dihydroxyphenyl)lactate
C23042  Atromentin
Reference
PMID:8550403
  Authors
Prieto MA, Diaz E, Garcia JL.
  Title
Molecular characterization of the 4-hydroxyphenylacetate catabolic pathway of Escherichia coli W: engineering a mobile aromatic degradative cluster.
  Journal
J Bacteriol 178:111-20 (1996)
DOI:10.1128/JB.178.1.111-120.1996
Reference
PMID:1194238
  Authors
Sparnins VL, Dagley S.
  Title
Alternative routes of aromatic catabolism in Pseudomonas acidovorans and Pseudomonas putida: gallic acid as a substrate and inhibitor of dioxygenases.
  Journal
J Bacteriol 124:1374-81 (1975)
DOI:10.1128/JB.124.3.1374-1381.1975
Reference
PMID:18435614
  Authors
Ito S, Wakamatsu K
  Title
Chemistry of mixed melanogenesis--pivotal roles of dopaquinone.
  Journal
Photochem Photobiol 84:582-92 (2008)
DOI:10.1111/j.1751-1097.2007.00238.x
Reference
PMID:11171088
  Authors
Olivares C, Jimenez-Cervantes C, Lozano JA, Solano F, Garcia-Borron JC
  Title
The 5,6-dihydroxyindole-2-carboxylic acid (DHICA) oxidase activity of human tyrosinase.
  Journal
Biochem J 354:131-9 (2001)
DOI:10.1042/bj3540131
Related
pathway
pvd00020  Citrate cycle (TCA cycle)
pvd00360  Phenylalanine metabolism
pvd00400  Phenylalanine, tyrosine and tryptophan biosynthesis
pvd00620  Pyruvate metabolism
pvd00650  Butanoate metabolism
KO pathway
ko00350   

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