Title of article :
Crystal Structure of a β-Catenin/Tcf Complex
Author/Authors :
Thomas A. Graham، نويسنده , , Carole Weaver، نويسنده , , Feng Mao، نويسنده , , David Kimelman، نويسنده , , Wenqing Xu، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2000
Pages :
12
From page :
885
To page :
896
Abstract :
The Wnt signaling pathway plays critical roles in embryonic development and tumorigenesis. Stimulation of the Wnt pathway results in the accumulation of a nuclear β-catenin/Tcf complex, activating Wnt target genes. A crystal structure of β-catenin bound to the β-catenin binding domain of Tcf3 (Tcf3-CBD) has been determined. The Tcf3-CBD forms an elongated structure with three binding modules that runs antiparallel to β-catenin along the positively charged groove formed by the armadillo repeats. Structure-based mutagenesis defines three sites in β-catenin that are critical for binding the Tcf3-CBD and are differentially involved in binding APC, cadherin, and Axin. The structural and mutagenesis data reveal a potential target for molecular drug design studies.
Journal title :
CELL
Serial Year :
2000
Journal title :
CELL
Record number :
1017207
Link To Document :
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