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Results 1 - 10 of 18 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171acetylated rhamnogalacturonan + H2O - Irpex lacteus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171acetylated rhamnogalacturonan + H2O - Irpex lacteus KY2902 ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171azurine dyed and cross-linked galactan + H2O - Aspergillus aculeatus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171MHR-S + H2O i.e. saponified modified hairy regions of rhamnogalacturonan I, from apple pectin, residue remaining after enzymatic liquefaction of pectin Aspergillus aculeatus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171MHR-S + H2O i.e. saponified modified hairy regions of rhamnogalacturonan I, from apple pectin, residue remaining after enzymatic liquefaction of pectin Aspergillus niger ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171more RGI endo-hydrolases, RGHs, attack the RGI backbone randomly in an endo-fashion and catalyse bond cleavage of alpha-(1->2) glycosidic bonds between D-GalpA and L-Rhap. The mechanism involves an inversion of the anomeric C1 configuration in galacturonic acid releasing oligosaccharides with beta-D-GalpA at the reducing end and L-Rhap at the non-reducing end as products Aspergillus niger ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171more RGI endo-hydrolases, RGHs, attack the RGI backbone randomly in an endo-fashion and catalyse bond cleavage of alpha-(1->2) glycosidic bonds between D-GalpA and L-Rhap. The mechanism involves an inversion of the anomeric C1 configuration in galacturonic acid releasing oligosaccharides with beta-D-GalpA at the reducing end and L-Rhap at the non-reducing end as products Aspergillus aculeatus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171more RGI endo-hydrolases, RGHs, attack the RGI backbone randomly in an endo-fashion and catalyse bond cleavage of alpha-(1->2) glycosidic bonds between D-GalpA and L-Rhap. The mechanism involves an inversion of the anomeric C1 configuration in galacturonic acid releasing oligosaccharides with beta-D-GalpA at the reducing end and L-Rhap at the non-reducing end as products. Aspergillus aculeatus RhgA catalyses the hydrolytic cleavage of the alpha-D-GalpA-(1->2)-alpha-L-Rhap glycosidic linkages thus releasing (oligomeric) products with Rhap at the non-reducing end Aspergillus aculeatus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171non-acetylated rhamnogalacturonan + H2O - Irpex lacteus ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 3.2.1.171non-acetylated rhamnogalacturonan + H2O - Irpex lacteus KY2902 ? - ?
Results 1 - 10 of 18 > >>