- Cell Biology
- Product Type
- Research Area
- New Products
- About Tocris
- Contact Us
Glycosylases are a group of enzymes that includes glucosidases, mannosidases and heparanases. There are two glucosidase subtypes, both found in the gut. They hydrolyze terminal (1,4)α-glucosidic linkages and (1,6)β-glucosidic linkages, liberating α-glucose and β-glucose.
|Cat. No.||Product Name / Activity|
|Glucosidase α inhibitor (intestinal)|
|Glucosidases α and β inhibitor|
|α-Mannosidase I inhibitor|
|Glucosidase I and II inhibitor|
|Inhibitor of class I α-mannosidases|
|α-glucosidase I and II inhibitor. Also inhibits ceramide-specific glycosyltransferases|
|6236||O8 OGG1 Inhibitor|
|Potent and selective 8-oxoguanine DNA glycosylase 1 (OGG1) inhibitor|
|Heparanase inhibitor. Antiangiogenic|
|Inhibitor of α-mannosidase II|
|6749||TH 5487 New|
|Selective 8-oxoguanine DNA glycosylase 1 (OGG1) inhibitor|
|Orally active α-glucosidase inhibitor|
Glycosylases are a group of enzymes that includes glucosidases, mannosidases and heparanases. There are two glucosidase subtypes, α- and β-glucosidase (EC numbers 184.108.40.206 and 220.127.116.11 respectively), which are both found in the gut. They hydrolyze terminal (1,4)α-glucosidic linkages and (1,6)β-glucosidic linkages, liberating α-glucose and β-glucose respectively.
Mannosidases are divided into two subtypes: I and II, (EC numbers 18.104.22.168 and 22.214.171.124 respectively) which display a wide expression pattern. Mannosidase I hydrolyzes (1,2)-linked α-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 and mannosidase II hydrolyzes (1,3)- and (1,6)-linked α-D-mannose residues in Man5(GlcNAc)3. Both subtypes require a divalent cation cofactor.
Heparanases are endo β-D-glucuronidase enzymes that cleave heparan sulfate side chains of heparan sulfate proteoglycans on cell surfaces and the extracellular matrix. Heparanases are involved in the clotting pathway and interact with tissue factor (TF) and TF pathway inhibitor (TFPI) to promote coagulation. Additional physiological roles include heparan sulfate turnover, embryo development, hair growth, and wound healing.
Inherited mutations in glucosidases can cause diseases such as Pompe disease (α-glucosidase deficiency) and mutations in mannosidases can cause mannosidosis (mannosidase I deficiency). Overexpression of heparanases is strongly implicated in tumor metastasis and angiogenesis.
Tocris offers the following scientific literature for Glycosylases to showcase our products. We invite you to request* or download your copy today!
*Please note that Tocris will only send literature to established scientific business / institute addresses.
Our new product guide highlights over 190 new products added to the Tocris Bioscience range during the second half of 2018.
|Gene||Species||Gene Symbol||Gene Accession No.||Protein Accession No.|
|Mannosidase I A1||Human||MAN1A1||NM_005907||P33908|
|Mannosidase I A2||Human||MAN1A2||NM_006699||O60476|
|Mannosidase I B1||Human||MAN1B1||NM_016219||Q9UKM7|
|Mannosidase I C1||Human||MAN1C1||NM_020379||Q9NR34|
|Mannosidase II A1||Human||MAN2A1||NM_002372||Q16706|
|Mannosidase II A2||Human||MAN2A2||NM_006122||P49641|
|Mannosidase II B1||Human||MAN2B1||NM_000528||O00754|
|Mannosidase II B2||Human||MAN2B2||NM_015274||Q9Y2E5|
|Mannosidase II C1||Human||MAN2C1||NM_006715||Q9NTJ4|