GDP-fucose protein O-fucosyltransferase 1

protein O-fucosyltransferase 1
Identifiers
Symbol	POFUT1
Entrez	23509
HUGO	14988
OMIM	607491
RefSeq	NM_172236
UniProt	Q9H488
Other data
EC number	2.4.1.221
Locus	Chr. 20 q11

GDP-fucose protein O-fucosyltransferase 1 (POFUT-1) is an enzyme belonging to the O-Fuc family of proteins all are involved in the transferring of o-fucose from GDP-β-L-fucose to substrates. POFUT-1 responsible for adding fucose sugars in O linkage to serine or threonine residues between the second and third conserved cysteines in EGF-like repeats on the Notch protein. The protein is an inverting glycosyltransferase, which means that the enzyme uses GDP-β-L-fucose as a donor substrate and transfers the fucose in O linkage to the protein producing fucose-α-O-serine/threonine.

When the gene for POFUT1 is knocked out, or the expression is decreased to very low levels, all Notch signaling is destroyed, which means that fucose on Notch is essential for Notch function. Why this is the case is not yet well understood.

Almost all glycosyltransferases reside in the Golgi apparatus. However, POFUT1 as well as the related enzyme POFUT2 have recently been shown to reside in the endoplasmic reticulum.

POFUT-1 is involved in the attachment of Fucose sugars to a lot of proteins, However a key pathway is the Post-transitional Modification of NOTCH signal proteins.

Pre-NOTCH proteins are translated and deposited in to the endoplasmic reticulum and are then first modified by POFUT-1 then by PGLUT-1 then exported the Golgi apparatus. in the endoplasmic reticulum POFUT-1 utilizes its sub-strait GDP-β-L-fucose as a donor for the five carbon sugar Fucose. fucose is then attached to a serine amino acid residue. Once Pre-notch is done being modified by POFUT-1 and POFUT-2, it is then exported to the Golgi apparatus where it is further modified and exported and incorporated into the cell membrane.

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