KEGG   PATHWAY: bpt00360Help
Entry
bpt00360                    Pathway                                

Name
Phenylalanine metabolism - Bordetella petrii
Class
Metabolism; Amino acid metabolism
BRITE hierarchy
Pathway map
bpt00360  Phenylalanine metabolism
bpt00360

Ortholog table
Other DBs
BSID: 62379
GO: 0006558
Organism
Bordetella petrii [GN:bpt]
Gene
Bpet4206  amine oxidase, flavin-containing [KO:K00274] [EC:1.4.3.4]
Bpet1935  paaK; phenylacetate-coenzyme A ligase [KO:K01912] [EC:6.2.1.30]
Bpet4737  putative phenylacetate-CoA ligase [KO:K01912] [EC:6.2.1.30]
Bpet1118  putative phenylacetate-CoA ligase [KO:K01912] [EC:6.2.1.30]
Bpet1934  paaI; phenylacetic acid degradation protein [KO:K02614] [EC:3.1.2.-]
Bpet1924  paaA; putative phenylacetic acid degradation protein [KO:K02609] [EC:1.14.13.149]
Bpet1925  paaB; phenylacetic acid degradation protein [KO:K02610]
Bpet1926  paaC; phenylacetic acid degradation protein [KO:K02611] [EC:1.14.13.149]
Bpet1927  paaD; phenylacetic acid degradation protein [KO:K02612]
Bpet1928  paaE; Predicted phenylacetic acid degradation NADH oxidoreductase [KO:K02613]
Bpet1933  paaG; enoyl-CoA hydratase probably involved in phenylacetate degradation [KO:K15866] [EC:5.3.3.18]
Bpet0817  enoyl-CoA hydratase [KO:K15866] [EC:5.3.3.18]
Bpet0373  hypothetical protein, probable enoyl-CoA hydratase/isomerase family member [KO:K15866] [EC:5.3.3.18]
Bpet3284  conserved hypothetical protein, enoyl-CoA hydratase/isomerase family member [KO:K01692] [EC:4.2.1.17]
Bpet0362  conserved hypothetical protein [KO:K01692] [EC:4.2.1.17]
Bpet0333  enoyl-CoA hydratase [KO:K01692] [EC:4.2.1.17]
Bpet0783  enoyl-CoA hydratase [KO:K01692] [EC:4.2.1.17]
Bpet2912  probable 3-hydroxybutyryl-CoA dehydrogenase [KO:K00074] [EC:1.1.1.157]
Bpet4524  probable 3-hydroxybutyryl-CoA dehydrogenase [KO:K00074] [EC:1.1.1.157]
Bpet0368  paaH; putative 3-hydroxybutyryl-CoA dehydrogenase [KO:K00074] [EC:1.1.1.157]
Bpet1243  hbd; 3-hydroxybutyryl-CoA dehydrogenase [KO:K00074] [EC:1.1.1.157]
Bpet4447  aspC; aspartate aminotransferase [KO:K00812] [EC:2.6.1.1]
Bpet3801  aspartate aminotransferase A [KO:K00812] [EC:2.6.1.1]
Bpet0137  hisC1; putative histidinol-phosphate aminotransferase [KO:K00817] [EC:2.6.1.9]
Bpet2024  hisC3; histidinol-phosphate aminotransferase [KO:K00817] [EC:2.6.1.9]
Bpet1886  hisC2; histidinol-phosphate aminotransferase [KO:K00817] [EC:2.6.1.9]
Bpet2781  tyrB; tyrB [KO:K00832] [EC:2.6.1.57]
Bpet1387  areB; Aryl-alcohol dehydrogenase [KO:K00055] [EC:1.1.1.90]
Bpet0681  bllY; putative 4-hydroxyphenylpyruvate dioxygenase [KO:K00457] [EC:1.13.11.27]
Bpet1992  D-amino acid dehydrogenase small subunit [KO:K00285] [EC:1.4.5.1]
Bpet2614  D-amino acid dehydrogenase small subunit [KO:K00285] [EC:1.4.5.1]
Bpet2578  D-amino acid dehydrogenase, small subunit [KO:K00285] [EC:1.4.5.1]
Bpet0709  D-amino acid dehydrogenase, small subunit [KO:K00285] [EC:1.4.5.1]
Bpet1260  dadA; D-amino acid dehydrogenase, small subunit [KO:K00285] [EC:1.4.5.1]
Bpet4806  D-alanine aminotransferase [KO:K00824] [EC:2.6.1.21]
Bpet3846  probable amidase [KO:K01426] [EC:3.5.1.4]
Bpet0304  putative 2-polyprenyl-6-methoxyphenol hydroxylase [KO:K05712] [EC:1.14.13.127]
Bpet4008  putative oxygenase [KO:K05712] [EC:1.14.13.127]
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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