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3S8Z

Crystal structure of LRP6-E3E4

Summary for 3S8Z
Entry DOI10.2210/pdb3s8z/pdb
Related3S8V 3S94
DescriptorLow-density lipoprotein receptor-related protein 6, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose (3 entities in total)
Functional Keywordswnt, receptor, lrp5, lrp6, ldl receptor-like protein, dickkopf (dkk), ywtd b-propeller, signaling protein
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight71916.77
Authors
Cheng, Z.,Xu, W. (deposition date: 2011-05-31, release date: 2011-10-26, Last modification date: 2023-09-13)
Primary citationCheng, 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: 21984209
DOI: 10.1038/nsmb.2139
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.8 Å)
Structure validation

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