3S8V

Crystal structure of LRP6-Dkk1 complex

3S8V の概要

• エントリーDOI: 10.2210/pdb3s8v/pdb
• 関連するPDBエントリー: 3S8Z 3S94
• 分子名称: Low-density lipoprotein receptor-related protein 6, Dickkopf-related protein 1 (2 entities in total)
• 機能のキーワード: wnt, receptor, lrp5, lrp6, ldl receptor-like protein, dickkopf (dkk), ywtd b-propeller, signaling protein
• 由来する生物種: Homo sapiens (human); 詳細
• 細胞内の位置: Membrane; Single-pass type I membrane protein: O75581; Secreted: O94907
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 151433.68

構造登録者

Cheng, Z.,Xu, W. (登録日: 2011-05-31, 公開日: 2011-10-26, 最終更新日: 2024-10-09)

主引用文献

Cheng, Z.,Biechele, T.,Wei, Z.,Morrone, S.,Moon, R.T.,Wang, L.,Xu, W.
Crystal structures of the extracellular domain of LRP6 and its complex with DKK1.
Nat.Struct.Mol.Biol., 18:1204-1210, 2011

PubMed Abstract: Low-density-lipoprotein (LDL) receptor-related proteins 5 and 6 (LRP5/6) are Wnt co-receptors essential for Wnt/β-catenin signaling. Dickkopf 1 (DKK1) inhibits Wnt signaling by interacting with the extracellular domains of LRP5/6 and is a drug target for multiple diseases. Here we present the crystal structures of a human LRP6-E3E4-DKK1 complex and the first and second halves of human LRP6's four propeller-epidermal growth factor (EGF) pairs (LRP6-E1E2 and LRP6-E3E4). Combined with EM analysis, these data demonstrate that LRP6-E1E2 and LRP6-E3E4 form two rigid structural blocks, with a short intervening hinge that restrains their relative orientation. The C-terminal domain of DKK1 (DKK1c) interacts with the top surface of the LRP6-E3 YWTD propeller and given their structural similarity, probably also that of the LRP6-E1 propeller, through conserved hydrophobic patches buttressed by a network of salt bridges and hydrogen bonds. Our work provides key insights for understanding LRP5/6 structure and the interaction of LRP5/6 with DKK, as well as for drug discovery.

PubMed: 21984209
DOI: 10.1038/nsmb.2139

実験手法

X-RAY DIFFRACTION (3.1 Å)