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. 1996 May 1;24(9):1727-33.
doi: 10.1093/nar/24.9.1727.

A 39 amino acid fragment of the cell cycle regulator p21 is sufficient to bind PCNA and partially inhibit DNA replication in vivo

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A 39 amino acid fragment of the cell cycle regulator p21 is sufficient to bind PCNA and partially inhibit DNA replication in vivo

J Chen et al. Nucleic Acids Res. .

Abstract

The cell cycle regulator p21 interacts with and inhibits the DNA replication and repair factor proliferating cell nuclear antigen (PCNA). We have defined a 39 amino acid fragment of p21 which is sufficient to bind PCNA with high affinity (Kd 10-20 nM). This peptide can inhibit DNA replication in vitro and microinjection of a GST fusion protein containing this domain inhibited S phase in vivo. Despite its high affinity for PCNA, the free 39 amino acid peptide does not have a well-defined structure, as judged from circular dichroism and nuclear magnetic resonance measurements, suggesting an induced fit mechanism for the PCNA-p21 interaction. The association of the small peptide with PCNA was thermolabile, suggesting that portions of p21 adjoining the minimal region of contact stabilize the interaction. In addition, a domain containing 67 amino acids from the N-terminus of PCNA was defined as both necessary and sufficient for binding to p21.

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    1. Curr Biol. 1994 Dec 1;4(12):1062-8 - PubMed
    1. Nature. 1995 Mar 23;374(6520):386-8 - PubMed
    1. Curr Biol. 1995 Mar 1;5(3):275-82 - PubMed
    1. Oncogene. 1995 Jun 15;10(12):2281-7 - PubMed
    1. Biochemistry. 1995 Jul 11;34(27):8869-75 - PubMed

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