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{ <http://www.tkuhn.ch/bel2nanopub/RA18UTQH99zdaJvh9_G4hE2CmXZZqO0Yiicw9xranLwM0#_5> ?p ?o ?g. }
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In vitro substrates included the translation repressor PHAS-I and the p53 protein. ATM phosphorylated p53 in vitro on a single residue, serine-15, which is phosphorylated in vivo in response to DNA damage
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