• Register
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.


Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.


Rad53 phosphorylation site clusters are important for Rad53 regulation and signaling.

Budding yeast Rad53 is an essential protein kinase that is phosphorylated and activated in a MEC1- and TEL1-dependent manner in response to DNA damage. We studied the role of Rad53 phosphorylation through mutation of consensus phosphorylation sites for upstream kinases Mec1 and Tel1. Alanine substitution of the Rad53 amino-terminal TQ cluster region reduced viability and impaired checkpoint functions. These substitution mutations spared the basal interaction with Asf1 and the DNA damage-induced interactions with Rad9. However, they caused a decrease in DNA damage-induced Rad53 kinase activity and an impaired interaction with the protein kinase Dun1. The Dun1 FHA (Forkhead-associated) domain recognized the amino-terminal TQ cluster of Rad53 after DNA damage or replication blockade. Thus, the phosphorylation of Rad53 by upstream kinases is important not only for Rad53 activation but also for creation of an interface between Rad53 and Dun1.

Pubmed ID: 12917350


  • Lee SJ
  • Schwartz MF
  • Duong JK
  • Stern DF


Molecular and cellular biology

Publication Data

September 14, 2003

Associated Grants

  • Agency: NCI NIH HHS, Id: R01CA82257
  • Agency: NIGMS NIH HHS, Id: T32GM07223

Mesh Terms

  • Alanine
  • Amino Acid Substitution
  • Binding Sites
  • Cell Cycle Proteins
  • Checkpoint Kinase 2
  • DNA Damage
  • Fungal Proteins
  • Intracellular Signaling Peptides and Proteins
  • MAP Kinase Kinase 1
  • Mitogen-Activated Protein Kinase Kinases
  • Mutation
  • Phosphorylation
  • Protein Kinases
  • Protein Structure, Tertiary
  • Protein-Serine-Threonine Kinases
  • Saccharomyces cerevisiae Proteins
  • Saccharomycetales
  • Schizosaccharomyces pombe Proteins
  • Signal Transduction