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Information on Organism Rhodococcus rhodochrous B-276

TaxTree of Organism Rhodococcus rhodochrous B-276
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EC NUMBER
COMMENTARY hide
PATHWAY
BRENDA Link
KEGG Link
MetaCyc Link
2-methylpropene degradation
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-
PWY-7778
2-nitrotoluene degradation
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-
PWY-5641
4-hydroxy-2-nonenal detoxification
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-
PWY-7112
acetone degradation II (to acetoacetate)
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PWY-5533
aerobic toluene degradation
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Benzoate degradation
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-
camalexin biosynthesis
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CAMALEXIN-SYN
Caprolactam degradation
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-
catechol degradation to 2-hydroxypentadienoate I
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-
P183-PWY
catechol degradation to 2-hydroxypentadienoate II
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PWY-5419
Chloroalkane and chloroalkene degradation
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-
Chlorocyclohexane and chlorobenzene degradation
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-
cutin biosynthesis
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-
PWY-321
Cutin, suberine and wax biosynthesis
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-
Drug metabolism - cytochrome P450
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Drug metabolism - other enzymes
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-
ethene and chloroethene degradation
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-
PWY-7776
Fatty acid degradation
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-
gliotoxin biosynthesis
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-
PWY-7533
Glutathione metabolism
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glutathione metabolism
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glutathione-mediated detoxification I
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PWY-4061
glutathione-mediated detoxification II
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-
PWY-6842
indole glucosinolate activation (intact plant cell)
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-
PWYQT-4477
isoprene degradation
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-
PWY-7777
Metabolic pathways
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Metabolism of xenobiotics by cytochrome P450
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Microbial metabolism in diverse environments
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octane oxidation
pentachlorophenol degradation
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-
PCPDEG-PWY
phenol degradation
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-
propanol degradation
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propene degradation
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PWY-5534
Styrene degradation
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-
toluene degradation II (aerobic) (via 4-methylcatechol)
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-
TOLUENE-DEG-3-OH-PWY
toluene degradation to 2-hydroxypentadienoate (via toluene-cis-diol)
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-
TOLUENE-DEG-DIOL-PWY
toluene degradation to 2-hydroxypentadienoate I (via o-cresol)
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TOLUENE-DEG-2-OH-PWY
traumatin and (Z)-3-hexen-1-yl acetate biosynthesis
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-
PWY-5410
vernolate biosynthesis III
-
-
PWY-6917
Xylene degradation
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-
ORGANISM
COMMENTARY hide
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
LINKS TO OTHER DATABASES (specific for Rhodococcus rhodochrous B-276)
NCBI: Taxonomy, PubMed, Genome