4KT1

Complex of R-spondin 1 with LGR4 extracellular domain

4KT1 の概要

• エントリーDOI: 10.2210/pdb4kt1/pdb
• 分子名称: Leucine-rich repeat-containing G-protein coupled receptor 4, R-spondin-1, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total)
• 機能のキーワード: r-spondin, lgr receptor, complex structure, wnt signaling, hormone receptor-cell adhesion complex, hormone receptor/cell adhesion
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 66164.89

構造登録者

Wang, X.Q.,Wang, D.L. (登録日: 2013-05-19, 公開日: 2013-06-19, 最終更新日: 2024-11-20)

主引用文献

Wang, D.L.,Huang, B.,Zhang, S.,Yu, X.,Wu, W.,Wang, X.Q.
Structural basis for R-spondin recognition by LGR4/5/6 receptors
Genes Dev., 27:1339-1344, 2013

PubMed Abstract: The R-spondin (RSPO) family of secreted proteins (RSPO1-RSPO4) has pleiotropic functions in development and stem cell growth by strongly enhancing Wnt pathway activation. Recently, leucine-rich repeat-containing G-protein-coupled receptor 4 (LGR4), LGR5, and LGR6 have been identified as receptors for RSPOs. Here we report the complex structure of the LGR4 extracellular domain (ECD) with the RSPO1 N-terminal fragment (RSPO1-2F) containing two adjacent furin-like cysteine-rich domains (FU-CRDs). The LGR4-ECD adopts the anticipated TLR horseshoe structure and uses its concave surface close to the N termini to bind RSPO1-2F. Both the FU-CRD1 and FU-CRD2 domains of RSPO1 contribute to LGR4 interaction, and binding and cellular assays identified critical RSPO1 residues for its biological activities. Our results define the molecular mechanism by which the LGR4/5/6 receptors recognize RSPOs and also provide structural insights into the signaling difference between the LGR4/5/6 receptors and other members in the LGR family.

PubMed: 23756652
DOI: 10.1101/gad.219360.113

実験手法

X-RAY DIFFRACTION (2.497 Å)