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<< < Results 41 - 50 of 60 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more phylogenetic analysis Alkalihalobacillus alcalophilus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more phylogenetic analysis Sporosarcina psychrophila ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more phylogenetic analysis Sporosarcina pasteurii ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more phylogenetic analysis Virgibacillus salexigens ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more phylogenetic analysis Chromohalobacter salexigens ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more the enzyme is osmoregulated in response to medium salinity allowing the organism to live in environments with high concentration of osmolytes Marinococcus halophilus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more ectoine synthase accepts more than one substrate and is a reversible enzyme able to catalyze both the intramolecular condensation into and the hydrolytic cleavage of cyclic amino acid derivatives. It forms 5-amino-3,4-dihydro-2H-pyrrole-2-carboxylate, ADPC, by cyclic condensation of glutamine in a reversible reaction. A number of ectoine derivatives, in particular 4,5-dihydro-2-methylimidazole-4-carboxylate and L-homoectoine, are also cleaved by ectoine synthase. Proposed reaction mechanism leading to L-ectoine and 5-amino-3,4-dihydro-2H-pyrrole-2-carboxylate, respectively, catalyzed by ectoine synthase, overview Halomonas elongata ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more EctC not only effectively converts its natural substrate N-gamma-acetyl-L-2,4-diaminobutyric acid into ectoine through a cyclocondensation reaction, but it can also use the isomer N-alpha-acetyl-L-2,4-diaminobutyric acid as its substrate, albeit with substantially reduced catalytic efficiency Sphingopyxis alaskensis ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more EctC not only effectively converts its natural substrate N-gamma-acetyl-L-2,4-diaminobutyric acid into ectoine through a cyclocondensation reaction, but it can also use the isomer N-alpha-acetyl-L-2,4-diaminobutyric acid as its substrate, albeit with substantially reduced catalytic efficiency Sphingopyxis alaskensis DSM 13593 / LMG 18877 / RB2256 ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.108more ectoine synthase accepts more than one substrate and is a reversible enzyme able to catalyze both the intramolecular condensation into and the hydrolytic cleavage of cyclic amino acid derivatives. It forms 5-amino-3,4-dihydro-2H-pyrrole-2-carboxylate, ADPC, by cyclic condensation of glutamine in a reversible reaction. A number of ectoine derivatives, in particular 4,5-dihydro-2-methylimidazole-4-carboxylate and L-homoectoine, are also cleaved by ectoine synthase. Proposed reaction mechanism leading to L-ectoine and 5-amino-3,4-dihydro-2H-pyrrole-2-carboxylate, respectively, catalyzed by ectoine synthase, overview Halomonas elongata DSM 2581 ? - ?
<< < Results 41 - 50 of 60 > >>