Matches in Nanopublications for { ?s ?p "HsCdc6 is an excellent substrate for Cdk2 in vitro and is phosphorylated in vivo at three sites (Ser-54, Ser-74, and Ser-106) that are phosphorylated by Cdk2 in vitro, strongly suggesting that HsCdc6 is an in vivo Cdk substrate . . . It is thought that Cdk phosphorylation of Cdc6p and Cdc18 triggers their degradation through a ubiquitination-mediated protein-degradation pathway (11?13)." ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- _5 value "HsCdc6 is an excellent substrate for Cdk2 in vitro and is phosphorylated in vivo at three sites (Ser-54, Ser-74, and Ser-106) that are phosphorylated by Cdk2 in vitro, strongly suggesting that HsCdc6 is an in vivo Cdk substrate . . . It is thought that Cdk phosphorylation of Cdc6p and Cdc18 triggers their degradation through a ubiquitination-mediated protein-degradation pathway (11?13)." provenance.
- _5 value "HsCdc6 is an excellent substrate for Cdk2 in vitro and is phosphorylated in vivo at three sites (Ser-54, Ser-74, and Ser-106) that are phosphorylated by Cdk2 in vitro, strongly suggesting that HsCdc6 is an in vivo Cdk substrate . . . It is thought that Cdk phosphorylation of Cdc6p and Cdc18 triggers their degradation through a ubiquitination-mediated protein-degradation pathway (11?13)." provenance.
- _5 value "HsCdc6 is an excellent substrate for Cdk2 in vitro and is phosphorylated in vivo at three sites (Ser-54, Ser-74, and Ser-106) that are phosphorylated by Cdk2 in vitro, strongly suggesting that HsCdc6 is an in vivo Cdk substrate . . . It is thought that Cdk phosphorylation of Cdc6p and Cdc18 triggers their degradation through a ubiquitination-mediated protein-degradation pathway (11?13)." provenance.
- _5 value "HsCdc6 is an excellent substrate for Cdk2 in vitro and is phosphorylated in vivo at three sites (Ser-54, Ser-74, and Ser-106) that are phosphorylated by Cdk2 in vitro, strongly suggesting that HsCdc6 is an in vivo Cdk substrate . . . It is thought that Cdk phosphorylation of Cdc6p and Cdc18 triggers their degradation through a ubiquitination-mediated protein-degradation pathway (11?13)." provenance.