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3HRN

crystal structure of a C-terminal coiled coil domain of Transient receptor potential (TRP) channel subfamily P member 2 (TRPP2, polycystic kidney disease 2)

3HRN の概要
エントリーDOI10.2210/pdb3hrn/pdb
関連するPDBエントリー3HRO
分子名称Transient receptor potential (TRP) channel subfamily P member 2 (TRPP2) (2 entities in total)
機能のキーワードcoiled coil, helix bundle, trimer, calcium, disease mutation, glycoprotein, ion transport, ionic channel, membrane, phosphoprotein, polymorphism, transmembrane, transport, transport protein
由来する生物種Homo sapiens (human)
細胞内の位置Cell projection, cilium membrane ; Multi-pass membrane protein : Q13563
タンパク質・核酸の鎖数1
化学式量合計7352.63
構造登録者
Yu, Y.,Ulbrich, M.H.,Li, M.-H.,Buraei, Z.,Chen, X.-Z.,Ong, A.C.M.,Tong, L.,Isacoff, E.Y.,Yang, J. (登録日: 2009-06-09, 公開日: 2009-07-28, 最終更新日: 2023-09-06)
主引用文献Yu, Y.,Ulbrich, M.H.,Li, M.H.,Buraei, Z.,Chen, X.Z.,Ong, A.C.,Tong, L.,Isacoff, E.Y.,Yang, J.
Structural and molecular basis of the assembly of the TRPP2/PKD1 complex.
Proc.Natl.Acad.Sci.USA, 106:11558-11563, 2009
Cited by
PubMed Abstract: Mutations in PKD1 and TRPP2 account for nearly all cases of autosomal dominant polycystic kidney disease (ADPKD). These 2 proteins form a receptor/ion channel complex on the cell surface. Using a combination of biochemistry, crystallography, and a single-molecule method to determine the subunit composition of proteins in the plasma membrane of live cells, we find that this complex contains 3 TRPP2 and 1 PKD1. A newly identified coiled-coil domain in the C terminus of TRPP2 is critical for the formation of this complex. This coiled-coil domain forms a homotrimer, in both solution and crystal structure, and binds to a single coiled-coil domain in the C terminus of PKD1. Mutations that disrupt the TRPP2 coiled-coil domain trimer abolish the assembly of both the full-length TRPP2 trimer and the TRPP2/PKD1 complex and diminish the surface expression of both proteins. These results have significant implications for the assembly, regulation, and function of the TRPP2/PKD1 complex and the pathogenic mechanism of some ADPKD-producing mutations.
PubMed: 19556541
DOI: 10.1073/pnas.0903684106
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 3hrn
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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