Recombinant Human B3GALTL protein (His tag) is a Human Fragment protein, in the 29 to 494 aa range, expressed in HEK 293, with >95% purity, < 1 EU/µg endotoxin level and suitable for SDS-PAGE.
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O-glucosyltransferase that transfers glucose toward fucose with a beta-1,3 linkage. Specifically glucosylates O-linked fucosylglycan on TSP type-1 domains of proteins, thereby contributing to elongation of O-fucosylglycan.
B3GALTL, B3GTL, B3GLCT, Beta3Glc-T, Beta 3-glucosyltransferase, Beta-3-glycosyltransferase-like
Recombinant Human B3GALTL protein (His tag) is a Human Fragment protein, in the 29 to 494 aa range, expressed in HEK 293, with >95% purity, < 1 EU/µg endotoxin level and suitable for SDS-PAGE.
pH: 7.4
Constituents: 100% PBS
O-glucosyltransferase that transfers glucose toward fucose with a beta-1,3 linkage. Specifically glucosylates O-linked fucosylglycan on TSP type-1 domains of proteins, thereby contributing to elongation of O-fucosylglycan.
Belongs to the glycosyltransferase 31 family.
The B3GALTL protein also known as beta-13-galactosyltransferase-like protein is an enzyme with an approximate mass of 65 kDa. It adds galactose to specific glycoproteins and plays a role in the O-fucosylation of thrombospondin type 1 repeats. B3GALTL is expressed in various tissues including the placenta and brain. It participates in glycosylation processes that are essential for protein function and stability within the cell.
The B3GALTL protein participates in glycosylation mechanisms necessary for the functionality of numerous proteins. This enzyme acts independently rather than as part of a complex to catalyze glycosidic bond formation which is integral to modifying proteins like Notch and Thrombospondin. It ensures that proteins acquire correct structural conformations optimizing their interactions and functions within the cellular environment.
B3GALTL engages in the Notch signaling pathway and the biosynthesis of glycan structures. This protein's glycosylation activity directly impacts these pathways influencing cellular communication and signaling. It interacts with proteins like fucosyltransferases within these processes further highlighting its role in modifying the activity and stability of signaling pathways vital for cellular functions.
B3GALTL mutations associate with Peters Plus syndrome a genetic condition characterized by developmental delays and eye abnormalities. Another disorder linked to this protein is Atrial Septal Defect associated with thrombosis abnormalities. In these contexts B3GALTL interacts with proteins involved in vascularization and ocular development emphasizing its importance in maintaining cellular and tissue homeostasis.
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