8PVU

Cryo-EM structure of DHS-ERK2 complex with 1:1 stoichiometry refined in C1 symmetry

8PVU の概要

• エントリーDOI: 10.2210/pdb8pvu/pdb
• EMDBエントリー: 17972
• 分子名称: Mitogen-activated protein kinase 1, Deoxyhypusine synthase (2 entities in total)
• 機能のキーワード: hypusination, transferase, protein-protein interaction, erk1/2 kinase-independent function, translation
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 5
• 化学式量合計: 205929.78

構造登録者

Kochanowski, P.,Biela, A.P.,Grudnik, P. (登録日: 2023-07-18, 公開日: 2024-10-16, 最終更新日: 2024-10-23)

主引用文献

Becker, A.E.,Kochanowski, P.,Wu, P.K.,Wator, E.,Chen, W.,Guchhait, K.,Biela, A.P.,Grudnik, P.,Park, J.I.
ERK1/2 interaction with DHPS regulates eIF5A deoxyhypusination independently of ERK kinase activity.
Cell Rep, 43:114831-114831, 2024

PubMed Abstract: This study explores a non-kinase effect of extracellular regulated kinases 1/2 (ERK1/2) on the interaction between deoxyhypusine synthase (DHPS) and its substrate, eukaryotic translation initiation factor 5A (eIF5A). We report that Raf/MEK/ERK activation decreases the DHPS-ERK1/2 interaction while increasing DHPS-eIF5A association in cells. We determined the cryoelectron microscopy (cryo-EM) structure of the DHPS-ERK2 complex at 3.5 Å to show that ERK2 hinders substrate entrance to the DHPS active site, subsequently inhibiting deoxyhypusination in vitro. In cells, impairing the ERK2 activation loop, but not the catalytic site, prolongs the DHPS-ERK2 interaction irrespective of Raf/MEK signaling. The ERK2 Ser-Pro-Ser motif, but not the common docking or F-site recognition sites, also regulates this complex. These data suggest that ERK1/2 dynamically regulate the DHPS-eIF5A interaction in response to Raf/MEK activity, regardless of its kinase function. In contrast, ERK1/2 kinase activity is necessary to regulate the expression of DHPS and eIF5A. These findings highlight an ERK1/2-mediated dual kinase-dependent and -independent regulation of deoxyhypusination.

PubMed: 39392755
DOI: 10.1016/j.celrep.2024.114831

実験手法

ELECTRON MICROSCOPY (3.5 Å)