3.2.1.171: rhamnogalacturonan hydrolase
This is an abbreviated version!
For detailed information about rhamnogalacturonan hydrolase, go to the full flat file.
Word Map on EC 3.2.1.171
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3.2.1.171
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aspergillus
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aculeatus
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pectic
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rgases
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galacturonic
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galactan
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homogalacturonans
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right-handed
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endo-polygalacturonase
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polygalacturonase
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irpex
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pectate
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lacteus
- 3.2.1.171
- aspergillus
- aculeatus
-
pectic
-
rgases
-
galacturonic
- galactan
- homogalacturonans
-
right-handed
- endo-polygalacturonase
- polygalacturonase
- irpex
- pectate
- lacteus
Reaction
Endohydrolysis of alpha-D-GalA-(1->2)-alpha-L-Rha glycosidic bond in the rhamnogalacturonan I backbone with initial inversion of anomeric configuration releasing oligosaccharides with beta-D-GalA at the reducing end =
Synonyms
endo-rhamnogalacturonase, HIRHG, RG hydrolase, RG-hydrolase, RGase A, RGH, RGI endo-hydrolase, RGI hydrolase, rhamnogalacturonan hydrolase, rhamnogalacturonase A, RhgA, RhgA_An, RhgB, RhgB_An
ECTree
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Reaction
Reaction on EC 3.2.1.171 - rhamnogalacturonan hydrolase
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Endohydrolysis of alpha-D-GalA-(1->2)-alpha-L-Rha glycosidic bond in the rhamnogalacturonan I backbone with initial inversion of anomeric configuration releasing oligosaccharides with beta-D-GalA at the reducing end
Endohydrolysis of alpha-D-GalA-(1->2)-alpha-L-Rha glycosidic bond in the rhamnogalacturonan I backbone with initial inversion of anomeric configuration releasing oligosaccharides with beta-D-GalA at the reducing end
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Endohydrolysis of alpha-D-GalA-(1->2)-alpha-L-Rha glycosidic bond in the rhamnogalacturonan I backbone with initial inversion of anomeric configuration releasing oligosaccharides with beta-D-GalA at the reducing end
mode of action and site of action, overview. 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
Endohydrolysis of alpha-D-GalA-(1->2)-alpha-L-Rha glycosidic bond in the rhamnogalacturonan I backbone with initial inversion of anomeric configuration releasing oligosaccharides with beta-D-GalA at the reducing end
mode of action and site of action, overview. 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