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人 HS3ST3B1 抗体对
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人 HS3ST3B1 抗体对

01AB00266

Heparan sulfate-glucosamine 3-sulfotransferase 3B1 (HS3ST3B1) is a type II integral membrane protein belonging to the 3-O-sulfotransferases family. It catalyzes the transfer of a sulfo group to an N-unsubstituted glucosamine linked to a 2-O-sulfo iduronic acid unit on heparan sulfate, using 3'-phospho-5'-adenylyl sulfate (PAPS) as a donor. This enzyme is involved in the modification of heparan sulfate, which plays a crucial role in various biological processes, including cell signaling and viral entry. Specifically, HS3ST3B1 generates an enzyme-modified heparan sulfate that acts as a binding receptor for Herpes simplex virus-1 (HSV-1), facilitating its entry into cells. The protein is encoded by the HS3ST3B1 gene located on chromosome 17 and has been associated with diseases such as Herpes simplex and overhydrated hereditary stomatocytosis.

Human
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技术参数

靶点基因名
HS3ST3B1
基因别名
3OST3B1; HS3ST3B
蛋白别名
heparan sulfate-glucosamine 3-sulfotransferase 3B1; HS3ST3B1
UniProt
Q9Y662
物种
Human

产品详情

靶点名称
HS3ST3B1
蛋白名称
heparan sulfate-glucosamine 3-sulfotransferase 3B1
蛋白别名
Heparan sulfate glucosamine 3-O-sulfotransferase 3B1; Heparan sulfate D-glucosaminyl 3-O-sulfotransferase 3B1; 3-OST-3B; Heparan sulfate 3-O-sulfotransferase 3B1; h3-OST-3B
靶点基因名
HS3ST3B1
基因别名
3OST3B1; HS3ST3B
UniProt
Q9Y662
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Heparan sulfate-glucosamine 3-sulfotransferase 3B1 (HS3ST3B1) is a type II integral membrane protein belonging to the 3-O-sulfotransferases family. It catalyzes the transfer of a sulfo group to an N-unsubstituted glucosamine linked to a 2-O-sulfo iduronic acid unit on heparan sulfate, using 3'-phospho-5'-adenylyl sulfate (PAPS) as a donor. This enzyme is involved in the modification of heparan sulfate, which plays a crucial role in various biological processes, including cell signaling and viral entry. Specifically, HS3ST3B1 generates an enzyme-modified heparan sulfate that acts as a binding receptor for Herpes simplex virus-1 (HSV-1), facilitating its entry into cells. The protein is encoded by the HS3ST3B1 gene located on chromosome 17 and has been associated with diseases such as Herpes simplex and overhydrated hereditary stomatocytosis.