Loading
PDBj
メニューPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

7NWJ

Solution NMR structure of the N-terminal domain of CEP164 (1-109)

7NWJ の概要
エントリーDOI10.2210/pdb7nwj/pdb
NMR情報BMRB: 50793
分子名称Centrosomal protein of 164 kDa (1 entity in total)
機能のキーワードcentriolar protein, ttbk2 binding, ciliopathies, protein binding
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数1
化学式量合計12950.51
構造登録者
van Breugel, M.,Rutherford, T.J. (登録日: 2021-03-16, 公開日: 2021-09-15, 最終更新日: 2024-06-19)
主引用文献Rosa E Silva, I.,Bino, L.,Johnson, C.M.,Rutherford, T.J.,Neuhaus, D.,Andreeva, A.,Cajanek, L.,van Breugel, M.
Molecular mechanisms underlying the role of the centriolar CEP164-TTBK2 complex in ciliopathies.
Structure, 30:114-128.e9, 2022
Cited by
PubMed Abstract: Cilia formation is essential for human life. One of the earliest events in the ciliogenesis program is the recruitment of tau-tubulin kinase 2 (TTBK2) by the centriole distal appendage component CEP164. Due to the lack of high-resolution structural information on this complex, it is unclear how it is affected in human ciliopathies such as nephronophthisis. Furthermore, it is poorly understood if binding to CEP164 influences TTBK2 activities. Here, we present a detailed biochemical, structural, and functional analysis of the CEP164-TTBK2 complex and demonstrate how it is compromised by two ciliopathic mutations in CEP164. Moreover, we also provide insights into how binding to CEP164 is coordinated with TTBK2 activities. Together, our data deepen our understanding of a crucial step in cilia formation and will inform future studies aimed at restoring CEP164 functionality in a debilitating human ciliopathy.
PubMed: 34499853
DOI: 10.1016/j.str.2021.08.007
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 7nwj
検証レポート(詳細版)ダウンロードをダウンロード

252456

件を2026-04-22に公開中

PDB statisticsPDBj update infoContact PDBjnumon