DNA damage induced hyperphosphorylation of replication protein A. 2. Characterization of DNA binding activity, protein interactions, and activity in DNA replication and repair.

No abstract is available for this paper.

• Publication year

  2005

• Venue

  Biochemistry

• Publication date

  2005-06-14

• Fields of study

  Biology, Medicine, Chemistry

• Identifiers
  DOI 10.1021/bi048057bPMID 15938633PMCID PMC4328999
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• UV-induced hyperphosphorylation of replication protein a depends on DNA replication and expression of ATM protein.

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• Damaged DNA-binding Protein DDB Stimulates the Excision of Cyclobutane Pyrimidine Dimers in Vitro in Concert with XPA and Replication Protein A*

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• Stopped-flow Kinetic Analysis of Replication Protein A-binding DNA

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• Adozelesin Triggers DNA Damage Response Pathways and Arrests SV40 DNA Replication through Replication Protein A Inactivation*

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• Werner syndrome protein: biochemical properties and functional interactions.

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  1999cited by this paper
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• Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair.

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• Synthesis of the Mammalian Telomere Lagging Strand in Vitro *

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• Replication protein A: a heterotrimeric, single-stranded DNA-binding protein required for eukaryotic DNA metabolism.

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• Interaction between replication protein A and p53 is disrupted after UV damage in a DNA repair-dependent manner.

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• Role of protein-protein interactions in the function of replication protein A (RPA): RPA modulates the activity of DNA polymerase alpha by multiple mechanisms.

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• A shuttle vector plasmid for studying carcinogen-induced point mutations in mammalian cells.

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