3S8V
Crystal structure of LRP6-Dkk1 complex
Summary for 3S8V
Entry DOI | 10.2210/pdb3s8v/pdb |
Related | 3S8Z 3S94 |
Descriptor | Low-density lipoprotein receptor-related protein 6, Dickkopf-related protein 1 (2 entities in total) |
Functional Keywords | wnt, receptor, lrp5, lrp6, ldl receptor-like protein, dickkopf (dkk), ywtd b-propeller, signaling protein |
Biological source | Homo sapiens (human) More |
Cellular location | Membrane; Single-pass type I membrane protein: O75581 Secreted: O94907 |
Total number of polymer chains | 3 |
Total formula weight | 151433.68 |
Authors | |
Primary citation | 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 Cited by 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: 21984209DOI: 10.1038/nsmb.2139 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.1 Å) |
Structure validation
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