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Word Map for Organism Nocardioides sp.
TaxTree of Organism Nocardioides sp.
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EC NUMBER 
COMMENTARY 
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PATHWAY
BRENDA Link
KEGG Link
MetaCyc Link
1,5-anhydrofructose degradation
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PWY-6992
2,4-dinitroanisole degradation
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PWY-7628
2,5-xylenol and 3,5-xylenol degradation
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PWY-7698
2-methylpropene degradation
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PWY-7778
2-nitrotoluene degradation
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PWY-5641
3,4-dichlorobenzoate degradation
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PWY-6217
3-chlorobenzoate degradation II (via protocatechuate)
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PWY-6216
4-hydroxy-2-nonenal detoxification
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PWY-7112
4-sulfocatechol degradation
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PWY-6041
acetate and ATP formation from acetyl-CoA III
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PWY-8328
acetate conversion to acetyl-CoA
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PWY0-1313
acetone degradation I (to methylglyoxal)
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PWY-5451
acetone degradation III (to propane-1,2-diol)
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PWY-7466
adenine and adenosine salvage III
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PWY-6609
adenine and adenosine salvage V
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PWY-6611
adenosine nucleotides degradation II
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SALVADEHYPOX-PWY
adlupulone and adhumulone biosynthesis
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PWY-7857
Amaryllidacea alkaloids biosynthesis
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PWY-7826
ammonia oxidation I (aerobic)
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AMMOXID-PWY
ammonia oxidation III
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PWY-2242
arachidonate metabolites biosynthesis
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PWY-8397
arsenate detoxification I
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PWY-8264
arsenate detoxification III
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PWY-8263
arsenic detoxification (plants)
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PWY-8259
arsenic detoxification (yeast)
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PWY-4621
arsenite to oxygen electron transfer (via azurin)
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PWY-7429
atrazine degradation I (aerobic)
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P141-PWY
atrazine degradation III
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PWY-5731
bacterial bioluminescence
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PWY-7723
biphenyl degradation
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PWY5F9-12
bupropion degradation
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PWY66-241
camalexin biosynthesis
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CAMALEXIN-SYN
carbazole degradation
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PWY-6550
catechol degradation to 2-hydroxypentadienoate I
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P183-PWY
catechol degradation to 2-hydroxypentadienoate II
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PWY-5419
catechol degradation to beta-ketoadipate
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CATECHOL-ORTHO-CLEAVAGE-PWY
chitin deacetylation
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PWY-7118
cis-geranyl-CoA degradation
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PWY-6672
colupulone and cohumulone biosynthesis
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PWY-5133
degradation of aromatic, nitrogen containing compounds
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dibenzothiophene desulfurization
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PWY-681
diphenyl ethers degradation
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PWY-7747
docosahexaenoate metabolites biosynthesis
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PWY-8400
ethanol degradation II
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PWY66-21
ethanol degradation III
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PWY66-161
ethanol degradation IV
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PWY66-162
ethene and chloroethene degradation
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PWY-7776
gentisate degradation I
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PWY-6223
gentisate degradation II
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PWY-7469
gliotoxin biosynthesis
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PWY-7533
glutathione-mediated detoxification I
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PWY-4061
glutathione-mediated detoxification II
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PWY-6842
glutathione-peroxide redox reactions
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PWY-4081
icosapentaenoate metabolites biosynthesis
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PWY-8399
indole glucosinolate activation (intact plant cell)
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PWYQT-4477
isoprene degradation
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PWY-7777
ketolysis
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PWY66-368
L-asparagine degradation II
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PWY-4002
L-isoleucine biosynthesis V
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PWY-5108
linoleate metabolites biosynthesis
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PWY-8395
lupulone and humulone biosynthesis
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PWY-5132
maresin biosynthesis
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PWY-8356
melatonin degradation I
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PWY-6398
methane oxidation to methanol I
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PWY-1641
methyl indole-3-acetate interconversion
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PWY-6303
methylsalicylate degradation
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PWY18C3-24
mRNA capping I
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PWY-7375
nicotine degradation I (pyridine pathway)
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P181-PWY
nicotine degradation III (VPP pathway)
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PWY-7128
nicotine degradation IV
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PWY66-201
nicotine degradation V
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PWY66-221
nitrite-dependent anaerobic methane oxidation
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PWY-6523
octane oxidation
pentachlorophenol degradation
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PCPDEG-PWY
poly-hydroxy fatty acids biosynthesis
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PWY-6710
propene degradation
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PWY-5534
protocatechuate degradation I (meta-cleavage pathway)
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P184-PWY
protocatechuate degradation II (ortho-cleavage pathway)
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PROTOCATECHUATE-ORTHO-CLEAVAGE-PWY
purine deoxyribonucleosides degradation I
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PWY-7179
purine deoxyribonucleosides degradation II
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PWY-7179-1
purine ribonucleosides degradation
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PWY0-1296
pyrimidine deoxyribonucleosides degradation
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PWY-7181
pyrimidine deoxyribonucleosides salvage
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PWY-7199
pyrimidine ribonucleosides degradation
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PWY0-1295
pyrimidine ribonucleosides salvage I
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PWY-7193
pyrimidine ribonucleosides salvage II
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PWY-6556
reductive glycine pathway of autotrophic CO2 fixation
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PWY-8303
retinol biosynthesis
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PWY-6857
S-methyl-5-thio-alpha-D-ribose 1-phosphate degradation I
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PWY-4361
salicylate degradation IV
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PWY-6640
sucrose biosynthesis I (from photosynthesis)
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SUCSYN-PWY
sucrose biosynthesis II
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PWY-7238
sucrose biosynthesis III
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PWY-7347
superpathway of methylsalicylate metabolism
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PWY18C3-25
TCA cycle VI (Helicobacter)
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REDCITCYC
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
vanillin biosynthesis I
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PWY-5665
octane oxidation
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P221-PWY
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ORGANISM
COMMENTARY
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
A0A096ZEC9: 2,4-dinitroanisole hydrolase A, A0A096ZED0: 2,4-dinitroanisole hydrolase B
UniProt
use of atrazine as sole nitrogen source and as sole carbon source. Comparison of degradation products with those from Pseudomonas sp. and Pseudoaminobacter sp.
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SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
SOURCE
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additional information
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strain JS614 grows on the C2 alkenes ethene, vinyl chloride, and vinyl fluoride as sole carbon sources. The presence of 400-800 microM ethene oxide extended the growth substrate range to propene and butene. Propene-dependent growth of JS614 is CO2-dependent and is prevented by the carboxylase/reductase inhibitor 2-bromoethanesulfonic acid, while growth on ethene is not CO2-dependent or 2-bromoethanesulfonic acid-sensitive. Propene oxide at 0.05-0.1 mM exerts inhibitory effects on growth of JS614 on both acetate and ethene, and on ethene oxide-induced growth on ethene
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LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY
GeneOntology No.
LITERATURE
SOURCE
: 
