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PMID: 17143292 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Review

beta-catenin destruction complex: insights and questions from a structural perspective.

Oncogene ·Vol. 25 ·No. 57 ·2006-12-04 ·Pages 7482-91

Kimelman D, Xu W

Abstract

At the heart of the canonical Wnt signaling pathway is the beta-catenin destruction complex, which functions in the absence of Wnt signaling to keep the cytosolic and nuclear levels of beta-catenin very low by promoting the phosphorylation and ubiquitination of beta-catenin. Structural studies, combined with other experimental approaches, have begun to provide important insights into the mechanism of the destruction complex. We suggest a working model for the destruction complex based on the existing structural and experimental data, and focus on the questions that this model and other studies have raised about the function of the complex in both the normal and Wnt-inhibited states.

MeSH Terms
Animals Cell Nucleus/metabolism Colonic Neoplasms/metabolism Cytosol/metabolism Humans Models, Biological Phosphorylation Protein Conformation Stem Cells/metabolism Ubiquitin/chemistry beta Catenin/chemistry,physiology
Chemicals
Ubiquitin beta Catenin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kimelman D
Department of Biochemistry, University of Washington, Seattle, WA 98195-7350, USA. kimelman@u.washington.edu
Xu W
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
2006-12-04
Pages
7482-91
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NCI NIH HHS · CA90351 · United States
NICHD NIH HHS · HD27262 · United States
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