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Results 1 - 10 of 38 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.21,2,3,5-tetrahydroxybenzene + 1,2,3-trihydroxybenzene 2,4,6,3’,4’,5’-hexahydroxydiphenyl ether and 3,4,5,3’,4’,5’-hexahydroxydiphenyl ether can substitute for the cocatalyst 1,2,3,5-tetrahydroxybenzene in vitro. This indicates that the diphenyl ethers can intrude into the active site and initiate the catalytic cycle Pelobacter acidigallici 1,3,5-trihydroxybenzene + 1,2,3,5-tetrahydroxybenzene - ?
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.21,2,3,5-tetrahydroxybenzene + pyrogallol - Pelobacter acidigallici ? - ?
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.21,2,3,5-tetrahydroxybenzene + pyrogallol key step in the anaerobic degradation of gallic acid and releated polyphenolic compounds Pelobacter acidigallici ? - ?
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.21,2,3,5-tetrahydroxybenzene + pyrogallol i.e. 1,2,3-trihydroxybenzene, reaction in fermentative degradation of trihydroxy-derivatives, pathway Pelobacter acidigallici ? - ?
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.21,2,3,5-tetrahydroxybenzene + pyrogallol i.e. 1,2,3-trihydroxybenzene, reaction in fermentative degradation of trihydroxy-derivatives, pathway Pelobacter acidigallici MaGal 2 ? - ?
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.21,2,3,5-tetrahydroxybenzene + pyrogallol key step in the anaerobic degradation of gallic acid and releated polyphenolic compounds Pelobacter acidigallici MaGal 2 ? - ?
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.2more dimethyl sulfoxide at unphysiological high concentrations can replace 1,2,3,5-tetrahydroxybenzene with 0.04% efficiency, no transhydroxylation takes place with catechol or phenol + 1,2,3,5-tetrahydroxybenzene, pyrogallol + catechol, resorcinol, hydroquinone or phenol Pelobacter acidigallici ? - ?
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.2more dimethyl sulfoxide at unphysiological high concentrations can replace 1,2,3,5-tetrahydroxybenzene with 0.04% efficiency, no transhydroxylation takes place with catechol or phenol + 1,2,3,5-tetrahydroxybenzene, pyrogallol + catechol, resorcinol, hydroquinone or phenol Pelobacter massiliensis ? - ?
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.2more intermolecular transhydroxylation Pelobacter acidigallici ? - ?
Show all pathways known for 1.97.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.97.1.2more 1,2,4,5-tetrahydroxybenzene: OH-donor, pyrogallol, hydroxyhydroquinone and resorcinol: OH-acceptors Pelobacter massiliensis ? - ?
Results 1 - 10 of 38 > >>