8GYN
zebrafish TIPE1 strucutre in complex with PE
8GYN の概要
| エントリーDOI | 10.2210/pdb8gyn/pdb |
| 分子名称 | Tumor necrosis factor alpha-induced protein 8-like protein 1, [(2~{R})-1-[2-azanylethoxy(oxidanyl)phosphoryl]oxy-3-hexadecanoyloxy-propan-2-yl] (~{Z})-octadec-9-enoate (3 entities in total) |
| 機能のキーワード | lipid transfer protein, tipe family, lipid binding protein |
| 由来する生物種 | Danio rerio (zebrafish) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 19405.52 |
| 構造登録者 | |
| 主引用文献 | Cao, S.,Zhang, Y.,Jiang, H.,Hou, X.,Wang, W. Structural insight into TIPE1 functioning as a lipid transfer protein. J.Biomol.Struct.Dyn., 41:14049-14062, 2023 Cited by PubMed Abstract: As a member of the tumor necrosis factor-α-induced protein 8 (TNFAIP8/TIPE) family, TIPE1 has been found to be associated with many cellular signaling pathways in regulating apoptosis, autophagy, and tumorigenesis. However, the position of TIPE1 in the signaling network remains elusive. Here we present the crystal structure of zebrafish TIPE1 in complex with phosphatidylethanolamine (PE) at a resolution of 1.38 Å. By comparison with structures of other three TIPE family proteins, a universal phospholipid-binding mode was proposed. Namely, the hydrophobic cavity binds to fatty acid tails, while 'X-R-R' triad nearby the entrance of cavity recognizes the phosphate group head. Using molecular dynamics (MD) simulations, we further elaborated the mechanism of how the lysine-rich N-terminal domain assisting TIPE1 to favorably bind to phosphatidylinositol (PI). Beside small molecule substrate, we identified Gαi3 as a direct-binding partner of TIPE1 using GST pull-down assay and size-exclusion chromatography. Analyses of key-residue mutations and predicted complex structure revealed that the binding mode of TIPE1 to Gαi3 could be non-canonical. In summary, our findings narrowed down TIPE1's position in Gαi3-related and PI-inducing signaling pathways.Communicated by Ramaswamy H. Sarma. PubMed: 36898854DOI: 10.1080/07391102.2023.2187641 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.38 Å) |
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