8VH5
Cryo-EM structure of Rab12-LRRK2 complex in the LRRK2 dimer state
8VH5 の概要
エントリーDOI | 10.2210/pdb8vh5/pdb |
EMDBエントリー | 43235 |
分子名称 | Leucine-rich repeat serine/threonine-protein kinase 2, Ras-related protein Rab-12, GUANOSINE-5'-DIPHOSPHATE, ... (6 entities in total) |
機能のキーワード | cryo-em, parkinson's disease, kinase, lrrk2, rab gtpases, hydrolase |
由来する生物種 | Homo sapiens (human) 詳細 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 616261.84 |
構造登録者 | |
主引用文献 | Li, X.,Zhu, H.,Huang, B.T.,Li, X.,Kim, H.,Tan, H.,Zhang, Y.,Choi, I.,Peng, J.,Xu, P.,Sun, J.,Yue, Z. RAB12-LRRK2 complex suppresses primary ciliogenesis and regulates centrosome homeostasis in astrocytes. Nat Commun, 15:8434-8434, 2024 Cited by PubMed Abstract: The leucine-rich repeat kinase 2 (LRRK2) phosphorylates a subset of RAB GTPases, and their phosphorylation levels are elevated by Parkinson's disease (PD)-linked mutations of LRRK2. However, the precise function of the LRRK2-regulated RAB GTPase in the brain remains to be elucidated. Here, we identify RAB12 as a robust LRRK2 substrate in the mouse brain through phosphoproteomics profiling and solve the structure of RAB12-LRRK2 protein complex through Cryo-EM analysis. Mechanistically, RAB12 cooperates with LRRK2 to inhibit primary ciliogenesis and regulate centrosome homeostasis in astrocytes through enhancing the phosphorylation of RAB10 and recruiting RILPL1, while the functions of RAB12 require a direct interaction with LRRK2 and LRRK2 activity. Furthermore, the ciliary and centrosome defects caused by the PD-linked LRRK2-G2019S mutation are prevented by Rab12 deletion in astrocytes. Thus, our study reveals a physiological function of the RAB12-LRRK2 complex in regulating ciliogenesis and centrosome homeostasis. The RAB12-LRRK2 structure offers a guidance in the therapeutic development of PD by targeting the RAB12-LRRK2 interaction. PubMed: 39343966DOI: 10.1038/s41467-024-52723-6 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (4 Å) |
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