Pathway | #Steps | #Present | #Specific |
acetate and ATP formation from acetyl-CoA III | 1 | 1 | 1 |
acetate conversion to acetyl-CoA | 1 | 1 | 1 |
benzoyl-CoA biosynthesis | 3 | 3 | 2 |
(R)- and (S)-3-hydroxybutanoate biosynthesis (engineered) | 5 | 4 | 3 |
oleate β-oxidation (thioesterase-dependent, yeast) | 2 | 2 | 1 |
acetoacetate degradation (to acetyl CoA) | 2 | 1 | 1 |
2-methyl-branched fatty acid β-oxidation | 14 | 10 | 6 |
5,6-dehydrokavain biosynthesis (engineered) | 10 | 6 | 4 |
fatty acid β-oxidation II (plant peroxisome) | 5 | 3 | 2 |
oleate β-oxidation | 35 | 30 | 12 |
superpathway of acetate utilization and formation | 3 | 3 | 1 |
ethanol degradation IV | 3 | 3 | 1 |
ketolysis | 3 | 3 | 1 |
ethanol degradation II | 3 | 3 | 1 |
valproate β-oxidation | 9 | 7 | 3 |
pyruvate fermentation to butanol II (engineered) | 6 | 4 | 2 |
ethanol degradation III | 3 | 2 | 1 |
L-isoleucine biosynthesis V | 3 | 2 | 1 |
polyhydroxybutanoate biosynthesis | 3 | 2 | 1 |
fatty acid β-oxidation I (generic) | 7 | 5 | 2 |
fatty acid β-oxidation VI (mammalian peroxisome) | 7 | 4 | 2 |
pyruvate fermentation to hexanol (engineered) | 11 | 8 | 3 |
(8E,10E)-dodeca-8,10-dienol biosynthesis | 11 | 6 | 3 |
(2S)-ethylmalonyl-CoA biosynthesis | 4 | 2 | 1 |
chitin deacetylation | 4 | 2 | 1 |
benzoate biosynthesis I (CoA-dependent, β-oxidative) | 9 | 3 | 2 |
4-hydroxybenzoate biosynthesis III (plants) | 5 | 5 | 1 |
adipate degradation | 5 | 5 | 1 |
adipate biosynthesis | 5 | 4 | 1 |
fatty acid β-oxidation IV (unsaturated, even number) | 5 | 4 | 1 |
ketogenesis | 5 | 3 | 1 |
propanoyl-CoA degradation II | 5 | 3 | 1 |
acrylate degradation I | 5 | 3 | 1 |
glutaryl-CoA degradation | 5 | 3 | 1 |
9-cis, 11-trans-octadecadienoyl-CoA degradation (isomerase-dependent, yeast) | 10 | 4 | 2 |
3-phenylpropanoate degradation | 10 | 4 | 2 |
benzoate biosynthesis III (CoA-dependent, non-β-oxidative) | 5 | 2 | 1 |
fatty acid β-oxidation VII (yeast peroxisome) | 5 | 2 | 1 |
isopropanol biosynthesis (engineered) | 5 | 1 | 1 |
pyruvate fermentation to acetone | 5 | 1 | 1 |
ethylbenzene degradation (anaerobic) | 5 | 1 | 1 |
fatty acid salvage | 6 | 6 | 1 |
β-alanine biosynthesis II | 6 | 5 | 1 |
L-isoleucine degradation I | 6 | 5 | 1 |
propanoate fermentation to 2-methylbutanoate | 6 | 4 | 1 |
methyl ketone biosynthesis (engineered) | 6 | 3 | 1 |
4-ethylphenol degradation (anaerobic) | 6 | 2 | 1 |
superpathway of bitter acids biosynthesis | 18 | 3 | 3 |
adlupulone and adhumulone biosynthesis | 6 | 1 | 1 |
10-trans-heptadecenoyl-CoA degradation (MFE-dependent, yeast) | 6 | 1 | 1 |
colupulone and cohumulone biosynthesis | 6 | 1 | 1 |
lupulone and humulone biosynthesis | 6 | 1 | 1 |
jasmonic acid biosynthesis | 19 | 4 | 3 |
(4Z,7Z,10Z,13Z,16Z)-docosapentaenoate biosynthesis (6-desaturase) | 13 | 2 | 2 |
superpathway of glyoxylate cycle and fatty acid degradation | 14 | 11 | 2 |
acetyl-CoA fermentation to butanoate | 7 | 4 | 1 |
benzoyl-CoA degradation I (aerobic) | 7 | 3 | 1 |
pyruvate fermentation to butanoate | 7 | 3 | 1 |
docosahexaenoate biosynthesis III (6-desaturase, mammals) | 14 | 2 | 2 |
mevalonate pathway II (haloarchaea) | 7 | 1 | 1 |
mevalonate pathway I (eukaryotes and bacteria) | 7 | 1 | 1 |
L-valine degradation I | 8 | 6 | 1 |
2-deoxy-D-ribose degradation II | 8 | 4 | 1 |
pyruvate fermentation to butanol I | 8 | 3 | 1 |
2-methylpropene degradation | 8 | 2 | 1 |
mevalonate pathway III (Thermoplasma) | 8 | 1 | 1 |
mevalonate pathway IV (archaea) | 8 | 1 | 1 |
isoprene biosynthesis II (engineered) | 8 | 1 | 1 |
androstenedione degradation I (aerobic) | 25 | 7 | 3 |
photosynthetic 3-hydroxybutanoate biosynthesis (engineered) | 26 | 19 | 3 |
phenylacetate degradation I (aerobic) | 9 | 9 | 1 |
4-oxopentanoate degradation | 9 | 5 | 1 |
superpathway of Clostridium acetobutylicum acidogenic fermentation | 9 | 5 | 1 |
reductive glycine pathway of autotrophic CO2 fixation | 9 | 5 | 1 |
cis-geranyl-CoA degradation | 9 | 2 | 1 |
superpathway of testosterone and androsterone degradation | 28 | 7 | 3 |
superpathway of coenzyme A biosynthesis II (plants) | 10 | 9 | 1 |
L-glutamate degradation V (via hydroxyglutarate) | 10 | 5 | 1 |
superpathway of geranylgeranyldiphosphate biosynthesis I (via mevalonate) | 10 | 4 | 1 |
L-lysine fermentation to acetate and butanoate | 10 | 3 | 1 |
methyl tert-butyl ether degradation | 10 | 2 | 1 |
superpathway of cholesterol degradation I (cholesterol oxidase) | 42 | 9 | 4 |
superpathway of phenylethylamine degradation | 11 | 11 | 1 |
Spodoptera littoralis pheromone biosynthesis | 22 | 4 | 2 |
ethylmalonyl-CoA pathway | 11 | 2 | 1 |
superpathway of cholesterol degradation II (cholesterol dehydrogenase) | 47 | 9 | 4 |
L-glutamate degradation VII (to butanoate) | 12 | 3 | 1 |
10-trans-heptadecenoyl-CoA degradation (reductase-dependent, yeast) | 12 | 2 | 1 |
10-cis-heptadecenoyl-CoA degradation (yeast) | 12 | 2 | 1 |
superpathway of Clostridium acetobutylicum solventogenic fermentation | 13 | 4 | 1 |
platensimycin biosynthesis | 26 | 6 | 2 |
1-butanol autotrophic biosynthesis (engineered) | 27 | 19 | 2 |
androstenedione degradation II (anaerobic) | 27 | 5 | 2 |
L-tryptophan degradation III (eukaryotic) | 15 | 3 | 1 |
glycerol degradation to butanol | 16 | 9 | 1 |
crotonate fermentation (to acetate and cyclohexane carboxylate) | 16 | 4 | 1 |
superpathway of Clostridium acetobutylicum acidogenic and solventogenic fermentation | 17 | 6 | 1 |
benzoate fermentation (to acetate and cyclohexane carboxylate) | 17 | 4 | 1 |
cholesterol degradation to androstenedione I (cholesterol oxidase) | 17 | 2 | 1 |
3-hydroxypropanoate/4-hydroxybutanate cycle | 18 | 9 | 1 |
toluene degradation VI (anaerobic) | 18 | 4 | 1 |
sitosterol degradation to androstenedione | 18 | 1 | 1 |
cholesterol degradation to androstenedione II (cholesterol dehydrogenase) | 22 | 2 | 1 |
superpathway of cholesterol degradation III (oxidase) | 49 | 5 | 2 |
superpathway of ergosterol biosynthesis I | 26 | 3 | 1 |
superpathway of cholesterol biosynthesis | 38 | 3 | 1 |
superpathway of L-lysine degradation | 43 | 23 | 1 |
Methanobacterium thermoautotrophicum biosynthetic metabolism | 56 | 21 | 1 |