KEGG   PATHWAY: syn00360Help
Entry
syn00360                    Pathway                                

Name
Phenylalanine metabolism - Synechocystis sp. PCC 6803
Class
Metabolism; Amino acid metabolism
BRITE hierarchy
Pathway map
syn00360  Phenylalanine metabolism
syn00360

Ortholog table
Other DBs
BSID: 780
GO: 0006558
Organism
Synechocystis sp. PCC 6803 [GN:syn]
Gene
slr0782  amine oxidase [KO:K00274] [EC:1.4.3.4]
sll0402  aspC; aspartate aminotransferase [KO:K00812] [EC:2.6.1.1]
sll1958  hisC; histidinol phosphate aminotransferase [KO:K00817] [EC:2.6.1.9]
slr0090  ppd; 4-hydroxyphenylpyruvic acid dioxgenase [KO:K00457] [EC:1.13.11.27]
sll1987  katG; catalase hpi [KO:K03782] [EC:1.11.1.21]
sll0828  nylA; 6-aminohexanoate-cyclic-dimer hydrolase [KO:K01426] [EC:3.5.1.4]
Compound
C00022  Pyruvate
C00024  Acetyl-CoA
C00042  Succinate
C00079  L-Phenylalanine
C00082  L-Tyrosine
C00083  Malonyl-CoA
C00084  Acetaldehyde
C00091  Succinyl-CoA
C00122  Fumarate
C00156  4-Hydroxybenzoate
C00166  Phenylpyruvate
C00180  Benzoate
C00223  p-Coumaroyl-CoA
C00323  Caffeoyl-CoA
C00406  Feruloyl-CoA
C00423  trans-Cinnamate
C00512  Benzoyl-CoA
C00582  Phenylacetyl-CoA
C00596  2-Hydroxy-2,4-pentadienoate
C00601  Phenylacetaldehyde
C00630  2-Methylpropanoyl-CoA
C00642  4-Hydroxyphenylacetate
C00755  4-Hydroxy-3-methoxy-benzaldehyde
C00805  Salicylate
C00811  4-Coumarate
C01198  3-(2-Hydroxyphenyl)propanoate
C01575  Ephedrine
C01586  Hippurate
C01772  trans-2-Hydroxycinnamate
C02137  alpha-Oxo-benzeneacetic acid
C02232  3-Oxoadipyl-CoA
C02265  D-Phenylalanine
C02505  2-Phenylacetamide
C02763  2-Hydroxy-3-phenylpropenoate
C02765  (+)-Pseudoephedrine
C03519  N-Acetyl-L-phenylalanine
C03589  4-Hydroxy-2-oxopentanoate
C04044  3-(2,3-Dihydroxyphenyl)propanoate
C04148  Phenylacetylglutamine
C04351  (R)-2-Methylimino-1-phenylpropan-1-ol
C04479  2-Hydroxy-6-oxonona-2,4-diene-1,9-dioate
C05332  Phenethylamine
C05593  3-Hydroxyphenylacetate
C05598  Phenylacetylglycine
C05607  Phenyllactate
C05620  N-Acetyl-D-phenylalanine
C05629  Phenylpropanoate
C05852  2-Hydroxyphenylacetate
C05853  Phenylethyl alcohol
C06207  2,6-Dihydroxyphenylacetate
C06866  Capsaicin
C07086  Phenylacetic acid
C07303  4-Hydroxy-3-methoxyphenyl-beta-hydroxypropanoyl-CoA
C08300  D-Cathine
C08301  D-Cathinone
C11457  3-(3-Hydroxyphenyl)propanoic acid
C11588  cis-3-(Carboxy-ethyl)-3,5-cyclo-hexadiene-1,2-diol
C12621  trans-3-Hydroxycinnamate
C12622  cis-3-(3-Carboxyethenyl)-3,5-cyclohexadiene-1,2-diol
C12623  trans-2,3-Dihydroxycinnamate
C12624  2-Hydroxy-6-ketononatrienedioate
C14144  5-Carboxy-2-pentenoyl-CoA
C14145  (3S)-3-Hydroxyadipyl-CoA
C15524  Phenylglyoxylyl-CoA
C16666  Vanillylamine
C16719  (-)-Norephedrine
C17268  Pyruvophenone
C18202  8-Methyl-6-nonenoic acid
C19945  3-Oxo-5,6-dehydrosuberyl-CoA
C19946  3-Oxo-5,6-dehydrosuberyl-CoA semialdehyde
C19975  2-Oxepin-2(3H)-ylideneacetyl-CoA
C20062  2-(1,2-Epoxy-1,2-dihydrophenyl)acetyl-CoA
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
Arai H, Yamamoto T, Ohishi T, Shimizu T, Nakata T, Kudo T.
  Title
Genetic organization and characteristics of the 3-(3-hydroxyphenyl)propionic acid degradation pathway of Comamonas testosteroni TA441.
  Journal
Microbiology 145 ( Pt 10):2813-20 (1999)
DOI:10.1099/00221287-145-10-2813
Reference
PMID:9603882
  Authors
Diaz E, Ferrandez A, Garcia JL.
  Title
Characterization of the hca cluster encoding the dioxygenolytic pathway for initial catabolism of 3-phenylpropionic acid in Escherichia coli K-12.
  Journal
J Bacteriol 180:2915-23 (1998)
Reference
PMID:9098055
  Authors
Ferrandez A, Garcia JL, Diaz E.
  Title
Genetic characterization and expression in heterologous hosts of the 3-(3-hydroxyphenyl)propionate catabolic pathway of Escherichia coli K-12.
  Journal
J Bacteriol 179:2573-81 (1997)
DOI:10.1128/JB.179.8.2573-2581.1997
Reference
  Authors
Hwang JY, Park J, Seo JH, Cha M, Cho BK, Kim J, Kim BG
  Title
Simultaneous synthesis of 2-phenylethanol and L-homophenylalanine using aromatic transaminase with yeast Ehrlich pathway.
  Journal
Biotechnol Bioeng 102:1323-9 (2009)
DOI:10.1002/bit.22178
Reference
  Authors
Teufel R, Mascaraque V, Ismail W, Voss M, Perera J, Eisenreich W, Haehnel W, Fuchs G
  Title
Bacterial phenylalanine and phenylacetate catabolic pathway revealed.
  Journal
Proc Natl Acad Sci U S A 107:14390-5 (2010)
DOI:10.1073/pnas.1005399107
KO pathway
ko00360   

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