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chaxamycin biosynthesis

State Icon Reaction EC-Number Confidence maximal confidence score from EnzymeDetector
3-amino-5-hydroxybenzoate + ATP + polyketide-[acp] <=> 3-amino-5-hydroxybenzoyl-[chaxamycin_PKS] + AMP + diphosphate 6.2.1.al

3-amino-5-hydroxybenzoyl-[chaxamycin_PKS] + (S)-methylmalonyl-CoA + malonyl-CoA + NADPH + H+ <=> tetraketide-[chaxamycin_PKS] + CoA + NADP+ + CO2 2.3.1

S-adenosyl-L-methionine + 3-demethylchaxamycin_B <=> S-adenosyl-L-homocysteine + chaxamycin_B + H+ 2.1.1

25-acetylchaxamycin_C + O2 + reduced_ferredoxin_[iron-sulfur]_cluster + H+ <=> chaxamycin_D + CO2 + H2O + oxidized_ferredoxin 1.14.15

prochaxamycin + acceptor <=> 3-demethylchaxamycin_A + reduced_acceptor not assigned

S-adenosyl-L-methionine + 3-demethylchaxamycin_A <=> S-adenosyl-L-homocysteine + chaxamycin_A + H+ 2.1.1

7-(3-amino-2,5-dihydroxyphenyl)-7-hydroxy-2,6-dimethyl-3,5-dioxoheptanoyl-[chaxamycin_PKS] + acceptor <=> 7-(5-amino-3,6-dioxocyclohexa-1,4-dien-1-yl)-7-hydroxy-2,6-dimethyl-3,5-dioxoheptanoyl-[chaxamycin_PKS] + reduced_acceptor not assigned

tetraketide-[chaxamycin_PKS] + O2 + NADPH + H+ <=> 7-(3-amino-2,5-dihydroxyphenyl)-7-hydroxy-2,6-dimethyl-3,5-dioxoheptanoyl-[chaxamycin_PKS] + H2O + NADP+ 1.14.13.M73

chaxamycin_A + O2 + reduced_ferredoxin_[iron-sulfur]_cluster + H+ <=> chaxamycin_C + H2O + oxidized_ferredoxin 1.14.15

prochaxamycin <=> 3-demethylchaxamycin_B + H2O not assigned

undecaketide-[chaxamycin-PKS] <=> prochaxamycin + polyketide-[acp] 2.3.1.M74

acetyl-CoA + chaxamycin_C <=> 25-acetylchaxamycin_C + CoA 2.3.1

7-(5-amino-3,6-dioxocyclohexa-1,4-dien-1-yl)-7-hydroxy-2,6-dimethyl-3,5-dioxoheptanoyl-[chaxamycin_PKS] + (S)-methylmalonyl-CoA + malonyl-CoA + NADPH + H+ <=> undecaketide-[chaxamycin-PKS] + CoA + NADP+ + CO2 + H2O 2.3.1

Visualization of the pathway