Molecular mechanisms of beta-catenin recognition by adenomatous polyposis coli revealed by the structure of an APC-beta-catenin complex.
The adenomatous polyposis coli (APC) tumor suppressor protein plays a critical role in regulating cellular levels of the oncogene product beta-catenin. APC binds to beta-catenin through a series of homologous 15 and 20 amino acid repeats. We have determined the crystal structure of a 15 amino acid beta-catenin binding repeat ... from APC bound to the armadillo repeat region of beta-catenin. Although it lacks significant sequence homology, the N-terminal half of the repeat binds in a manner similar to portions of E-cadherin and XTcf3, but the remaining interactions are unique to APC. We discuss the implications of this new structure for the design of therapeutics, and present evidence from structural, biochemical and sequence data, which suggest that the 20 amino acid repeats can adopt two modes of binding to beta-catenin.
Mesh Terms:
Adenomatous Polyposis Coli, Adenomatous Polyposis Coli Protein, Amino Acid Sequence, Cadherins, Crystallography, X-Ray, Cytoskeletal Proteins, HMGB Proteins, Humans, Ligands, Models, Molecular, Molecular Sequence Data, Peptides, Plasmids, Protein Binding, Protein Biosynthesis, Protein Structure, Tertiary, Sequence Homology, Amino Acid, TCF Transcription Factors, Trans-Activators, Transcription Factors, beta Catenin
Adenomatous Polyposis Coli, Adenomatous Polyposis Coli Protein, Amino Acid Sequence, Cadherins, Crystallography, X-Ray, Cytoskeletal Proteins, HMGB Proteins, Humans, Ligands, Models, Molecular, Molecular Sequence Data, Peptides, Plasmids, Protein Binding, Protein Biosynthesis, Protein Structure, Tertiary, Sequence Homology, Amino Acid, TCF Transcription Factors, Trans-Activators, Transcription Factors, beta Catenin
EMBO J.
Date: Nov. 15, 2001
PubMed ID: 11707392
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