From: Investigating hookworm genomes by comparative analysis of two Ancylostoma species
 | AC | Clusters per library |  | AE | Clusters per library |  | Total # of enzymes in KEGG | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
KEGG CATEGORY REPRESENTEDa | Clb | iL3 | taL3 | ssL3 | Mixed | Enzc | Clb | iL3 | Ad | Mixed | Enzc | Â |
1. Carbohydrate metabolism | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   1.1 Glycolysis / Gluconeogenesis | 23 | 13 | 0 | 5 | 5 | 22 | 25 | 10 | 11 | 4 | 23 | 40 |
   1.2 Citrate cycle (TCA cycle) | 17 | 8 | 0 | 4 | 5 | 16 | 15 | 4 | 8 | 3 | 15 | 23 |
   1.3 Pentose phosphate pathway | 9 | 3 | 0 | 4 | 2 | 9 | 12 | 5 | 3 | 4 | 8 | 34 |
   1.4 Pentose and glucuronate interconversions | 8 | 3 | 0 | 3 | 2 | 9 | 9 | 5 | 4 | 0 | 8 | 53 |
   1.5 Fructose and mannose metabolism | 14 | 6 | 0 | 4 | 4 | 15 | 20 | 7 | 11 | 2 | 15 | 61 |
   1.6 Galactose metabolism | 10 | 4 | 0 | 4 | 2 | 8 | 12 | 6 | 5 | 1 | 12 | 37 |
   1.7 Ascorbate and aldarate metabolism | 7 | 4 | 0 | 2 | 1 | 4 | 5 | 5 | 0 | 0 | 4 | 29 |
   1.8 Pyruvate metabolism | 25 | 11 | 0 | 11 | 3 | 23 | 27 | 8 | 17 | 2 | 26 | 67 |
   1.9 Glyoxylate and dicarboxylate metabolism | 13 | 6 | 0 | 5 | 2 | 14 | 9 | 1 | 5 | 3 | 17 | 58 |
   1.10 Propanoate metabolism | 22 | 7 | 1 | 10 | 4 | 20 | 25 | 11 | 8 | 6 | 22 | 46 |
   1.11 Butanoate metabolism | 22 | 9 | 1 | 7 | 5 | 23 | 29 | 14 | 14 | 1 | 26 | 52 |
   1.12 C5-Branched dibasic acid metabolism | 4 | 3 | 0 | 1 | 0 | 2 | 2 | 1 | 0 | 1 | 1 | 20 |
   1.13 Inositol metabolism | 6 | 2 | 0 | 1 | 3 | 4 | 7 | 2 | 3 | 2 | 4 | 5 |
2. Energy metabolism | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   2.1 Oxidative phosphorylation | 24 | 7 | 0 | 6 | 11 | 11 | 33 | 10 | 14 | 9 | 13 | 14 |
   2.2 ATP synthesis | 8 | 2 | 0 | 3 | 3 | 1 | 11 | 4 | 3 | 4 | 1 | 1 |
   2.4 Carbon fixation | 11 | 3 | 0 | 3 | 5 | 11 | 11 | 3 | 5 | 3 | 13 | 23 |
   2.5 Reductive carboxylate cycle (CO2 fixation) | 12 | 7 | 0 | 1 | 4 | 8 | 9 | 2 | 4 | 3 | 7 | 13 |
   2.6 Methane metabolism | 6 | 4 | 0 | 0 | 2 | 5 | 6 | 0 | 4 | 2 | 6 | 26 |
   2.7 Nitrogen metabolism | 11 | 2 | 0 | 5 | 4 | 14 | 12 | 5 | 5 | 2 | 15 | 64 |
   2.8 Sulfur metabolism | 5 | 1 | 0 | 1 | 3 | 9 | 6 | 3 | 1 | 2 | 9 | 30 |
3. Lipid metabolism | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   3.1 Fatty acid biosynthesis (path 1) | 6 | 2 | 0 | 3 | 1 | 11 | 7 | 3 | 3 | 1 | 6 | 14 |
   3.2 Fatty acid biosynthesis (path 2) | 8 | 2 | 0 | 5 | 1 | 6 | 6 | 3 | 2 | 1 | 5 | 8 |
   3.3 Fatty acid metabolism | 14 | 6 | 1 | 6 | 1 | 17 | 21 | 13 | 7 | 1 | 16 | 28 |
   3.4 Synthesis and degradation of ketone bodies | 2 | 0 | 0 | 1 | 1 | 2 | 8 | 4 | 3 | 1 | 3 | 6 |
   3.5 Sterol biosynthesis | 4 | 1 | 1 | 2 | 0 | 4 | 4 | 2 | 2 | 0 | 9 | 35 |
   3.6 Bile acid biosynthesis | 11 | 7 | 1 | 2 | 1 | 11 | 11 | 6 | 4 | 1 | 10 | 27 |
   3.8 Androgen and estrogen metabolism | 7 | 5 | 0 | 2 | 0 | 9 | 7 | 4 | 3 | 0 | 8 | 26 |
4. Nucleotide metabolism | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   4.1 Purine metabolism | 27 | 11 | 0 | 11 | 5 | 28 | 32 | 14 | 11 | 7 | 32 | 99 |
   4.2 Pyrimidine metabolism | 16 | 8 | 1 | 5 | 2 | 15 | 22 | 9 | 12 | 1 | 22 | 61 |
   4.3 Nucleotide sugars metabolism | 6 | 4 | 0 | 0 | 2 | 3 | 4 | 2 | 2 | 0 | 4 | 30 |
5. Amino acid metabolism | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   5.1 Glutamate metabolism | 11 | 3 | 0 | 5 | 3 | 14 | 16 | 8 | 7 | 1 | 18 | 36 |
   5.2 Alanine and aspartate metabolism | 14 | 1 | 0 | 8 | 5 | 15 | 14 | 5 | 6 | 3 | 15 | 38 |
   5.3 Glycine, serine and threonine metabolism | 19 | 7 | 0 | 9 | 3 | 14 | 21 | 8 | 10 | 3 | 24 | 56 |
   5.4 Methionine metabolism | 6 | 1 | 0 | 4 | 1 | 9 | 6 | 5 | 1 | 0 | 8 | 24 |
   5.5 Cysteine metabolism | 8 | 2 | 0 | 2 | 4 | 11 | 7 | 5 | 2 | 0 | 9 | 23 |
   5.6 Valine, leucine and isoleucine degradation | 16 | 3 | 1 | 8 | 4 | 16 | 22 | 11 | 6 | 5 | 18 | 32 |
   5.7 Valine, leucine and isoleucine biosynthesis | 7 | 1 | 0 | 4 | 2 | 7 | 9 | 6 | 2 | 1 | 8 | 15 |
   5.8 Lysine biosynthesis | 11 | 1 | 0 | 6 | 4 | 10 | 9 | 4 | 3 | 2 | 8 | 31 |
   5.9 Lysine degradation | 19 | 8 | 0 | 8 | 3 | 14 | 19 | 12 | 6 | 1 | 17 | 47 |
   5.10 Arginine and proline metabolism | 18 | 4 | 0 | 8 | 6 | 20 | 22 | 11 | 7 | 4 | 20 | 71 |
   5.11 Histidine metabolism | 10 | 4 | 0 | 4 | 2 | 8 | 10 | 5 | 4 | 1 | 8 | 39 |
   5.12 Tyrosine metabolism | 18 | 8 | 0 | 7 | 3 | 19 | 19 | 11 | 5 | 3 | 19 | 67 |
   5.13 Phenylalanine metabolism | 13 | 5 | 0 | 3 | 5 | 11 | 14 | 7 | 6 | 1 | 12 | 40 |
   5.14 Tryptophan metabolism | 17 | 8 | 0 | 8 | 1 | 15 | 22 | 16 | 4 | 2 | 18 | 61 |
   5.15 Phenylalanine, tyrosine and tryptophan biosynthesis | 5 | 1 | 0 | 2 | 2 | 6 | 4 | 2 | 0 | 2 | 7 | 31 |
   5.16 Urea cycle and metabolism of amino groups | 10 | 1 | 0 | 5 | 4 | 14 | 10 | 2 | 6 | 2 | 11 | 35 |
6. Metabolism of other amino acids | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   6.1 beta-Alanine metabolism | 14 | 4 | 1 | 7 | 2 | 13 | 11 | 8 | 1 | 2 | 10 | 32 |
   6.2 Taurine and hypotaurine metabolism | 1 | 0 | 0 | 0 | 1 | 1 | 2 | 2 | 0 | 0 | 3 | 14 |
   6.3 Aminophosphonate metabolism | 4 | 0 | 0 | 3 | 1 | 3 | 5 | 2 | 3 | 0 | 5 | 15 |
   6.4 Selenoamino acid metabolism | 7 | 0 | 0 | 4 | 3 | 12 | 12 | 6 | 4 | 2 | 15 | 22 |
   6.5 Cyanoamino acid metabolism | 2 | 1 | 0 | 1 | 0 | 1 | 7 | 5 | 1 | 1 | 6 | 19 |
   6.6 D-Glutamine and D-glutamate metabolism | 2 | 0 | 0 | 1 | 1 | 2 | 2 | 1 | 0 | 1 | 2 | 12 |
   6.7 D-Arginine and D-ornithine metabolism | 3 | 1 | 0 | 0 | 2 | 2 | 3 | 0 | 2 | 1 | 2 | 10 |
   6.9 Glutathione metabolism | 5 | 1 | 0 | 0 | 4 | 4 | 9 | 5 | 3 | 1 | 6 | 27 |
7. Metabolism of complex carbohydrates | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   7.1 Starch and sucrose metabolism | 18 | 2 | 0 | 13 | 3 | 18 | 20 | 13 | 6 | 1 | 20 | 75 |
   7.2 N-Glycans biosynthesis | 7 | 4 | 0 | 1 | 2 | 7 | 7 | 2 | 4 | 1 | 9 | 27 |
   7.3 O-Glycans biosynthesis | 3 | 1 | 0 | 1 | 1 | 2 | 6 | 5 | 1 | 0 | 3 | 8 |
   7.5 Aminosugars metabolism | 6 | 3 | 0 | 2 | 1 | 6 | 10 | 5 | 5 | 0 | 10 | 39 |
   7.8 Glycosaminoglycan degradation | 1 | 1 | 0 | 0 | 0 | 1 | 1 | 1 | 0 | 0 | 1 | 13 |
   7.9 Chondroitin / Heparan sulfate biosynthesis | 5 | 3 | 0 | 1 | 1 | 4 | 6 | 2 | 4 | 0 | 4 | 18 |
   7.10 Keratan sulfate biosynthesis | 1 | 0 | 0 | 1 | 0 | 1 | 2 | 1 | 1 | 0 | 1 | 6 |
8. Metabolism og complex lipids | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   8.1 Glycerolipid metabolism | 24 | 10 | 0 | 9 | 5 | 22 | 25 | 10 | 13 | 2 | 22 | 80 |
   8.3 Inositol phosphate metabolism | 8 | 4 | 0 | 4 | 0 | 4 | 8 | 5 | 2 | 1 | 3 | 25 |
   8.4 Sphingophospholipid biosynthesis | 1 | 1 | 0 | 0 | 0 | 1 | 2 | 1 | 1 | 0 | 2 | 8 |
   8.5 Phospholipid degradation | 3 | 2 | 0 | 0 | 1 | 3 | 1 | 1 | 0 | 0 | 1 | 11 |
   8.6 Sphingoglycolipid metabolism | 11 | 1 | 1 | 9 | 0 | 7 | 10 | 8 | 2 | 0 | 4 | 20 |
   8.9 Globoside metabolism | 2 | 1 | 0 | 1 | 0 | 2 | 2 | 1 | 1 | 0 | 1 | 12 |
   8.11 Prostaglandin and leukotriene metabolism | 8 | 2 | 0 | 1 | 5 | 8 | 7 | 4 | 3 | 0 | 6 | 19 |
9. Metabolism of cofactors and vitamins | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   9.2 Riboflavin metabolism | 4 | 1 | 0 | 3 | 0 | 2 | 2 | 2 | 0 | 0 | 2 | 13 |
   9.3 Vitamin B6 metabolism | 6 | 4 | 0 | 1 | 1 | 3 | 6 | 4 | 1 | 1 | 5 | 23 |
   9.4 Nicotinate and nicotinamide metabolism | 11 | 2 | 0 | 7 | 2 | 7 | 15 | 8 | 7 | 0 | 7 | 32 |
   9.5 Pantothenate and CoA biosynthesis | 8 | 2 | 0 | 4 | 2 | 9 | 8 | 6 | 2 | 0 | 7 | 27 |
   9.7 Folate biosynthesis | 5 | 2 | 1 | 0 | 2 | 5 | 6 | 1 | 4 | 1 | 5 | 25 |
   9.8 One carbon pool by folate | 5 | 3 | 0 | 2 | 0 | 10 | 7 | 3 | 3 | 1 | 8 | 24 |
   9.10 Porphyrin and chlorophyll metabolism | 18 | 4 | 0 | 10 | 4 | 12 | 27 | 15 | 8 | 4 | 13 | 56 |
   9.11 Ubiquinone biosynthesis | 19 | 10 | 0 | 5 | 4 | 13 | 28 | 11 | 14 | 3 | 14 | 22 |
10. Biosynthesis of secondary metabolites | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   10.1 Terpenoid biosynthesis | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 0 | 2 | 0 | 4 | 12 |
   10.3 Flavonoids, stilbene and lignin biosynthesis | 6 | 3 | 0 | 1 | 2 | 7 | 8 | 5 | 3 | 0 | 7 | 39 |
   10.4 Alkaloid biosynthesis I | 5 | 2 | 0 | 3 | 0 | 6 | 3 | 3 | 0 | 0 | 5 | 36 |
   10.8 Streptomycin biosynthesis | 2 | 0 | 0 | 2 | 0 | 3 | 4 | 2 | 1 | 1 | 4 | 14 |
   10.9 Erythromycin biosynthesis | 2 | 0 | 0 | 2 | 0 | 3 | 3 | 2 | 1 | 0 | 3 | 6 |
11. Biodegradation of xenobiotics | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â | Â |
   11.4 Nitrobenzene degradation | 4 | 1 | 0 | 3 | 0 | 5 | 4 | 2 | 1 | 1 | 3 | 17 |
   11.9 Tetrachloroethene degradation | 6 | 4 | 0 | 1 | 1 | 3 | 2 | 2 | 0 | 0 | 3 | 5 |
   11.10 Styrene degradation | 4 | 2 | 0 | 2 | 0 | 3 | 6 | 5 | 0 | 1 | 5 | 18 |
   11.1 gamma-Hexachlorocyclohexane degradation | 6 | 3 | 0 | 3 | 0 | 5 | 5 | 3 | 2 | 0 | 4 | 12 |
   11.1 Fluorene degradation | 3 | 1 | 0 | 2 | 0 | 4 | 2 | 2 | 0 | 0 | 2 | 13 |
   11.2 Benzoate degradation via CoA ligation | 22 | 8 | 1 | 10 | 3 | 18 | 25 | 14 | 10 | 1 | 18 | 38 |
   11.2 Benzoate degradation via hydroxylation | 7 | 2 | 0 | 5 | 0 | 7 | 5 | 4 | 1 | 0 | 5 | 45 |