Mutation of the serine 312 phosphorylation site does not alter the ability of mouse p53 to inhibit simian virus 40 DNA replication in vivo.
about
Human DNA-activated protein kinase phosphorylates serines 15 and 37 in the amino-terminal transactivation domain of human p53.The p53 tumour suppressor protein is phosphorylated at serine 389 by casein kinase II.Nuclear protein phosphorylation and growth control.Activities and response to DNA damage of latent and active sequence-specific DNA binding forms of mouse p53.Simian virus 40 can overcome the antiproliferative effect of wild-type p53 in the absence of stable large T antigen-p53 binding.Phosphorylation sites in the amino-terminal region of mouse p53.Altered phosphorylation of free and bound forms of monkey p53 and simian virus 40 large T antigen during lytic infection.Mutation of the casein kinase II phosphorylation site abolishes the anti-proliferative activity of p53.p53 is covalently linked to 5.8S rRNA.Growth inhibition by anchorage-deficiency is associated with increased level but reduced phosphorylation of mutant p53.
P2860
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P2860
Mutation of the serine 312 phosphorylation site does not alter the ability of mouse p53 to inhibit simian virus 40 DNA replication in vivo.
description
1990 nî lūn-bûn
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1990年の論文
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name
Mutation of the serine 312 pho ...... us 40 DNA replication in vivo.
@ast
Mutation of the serine 312 pho ...... us 40 DNA replication in vivo.
@en
type
label
Mutation of the serine 312 pho ...... us 40 DNA replication in vivo.
@ast
Mutation of the serine 312 pho ...... us 40 DNA replication in vivo.
@en
prefLabel
Mutation of the serine 312 pho ...... us 40 DNA replication in vivo.
@ast
Mutation of the serine 312 pho ...... us 40 DNA replication in vivo.
@en
P2860
P1433
P1476
Mutation of the serine 312 pho ...... us 40 DNA replication in vivo.
@en
P2093
P2860
P304
P407
P577
1990-04-01T00:00:00Z