4GS6

Irreversible Inhibition of TAK1 Kinase by 5Z-7-Oxozeaenol

4GS6 の概要

• エントリーDOI: 10.2210/pdb4gs6/pdb
• 関連するPDBエントリー: 2EVA
• 分子名称: Tak1-Tab1 fusion protein, 1,2-ETHANEDIOL, (3S,5Z,8S,9S,11E)-8,9,16-trihydroxy-14-methoxy-3-methyl-3,4,9,10-tetrahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione, ... (4 entities in total)
• 機能のキーワード: kinase fold, tab1 binding, cytosol, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 36503.97

構造登録者

Larsen, N.A.,Ferguson, A.D.,Wu, J. (登録日: 2012-08-27, 公開日: 2013-01-23, 最終更新日: 2024-11-06)

主引用文献

Wu, J.,Powell, F.,Larsen, N.A.,Lai, Z.,Byth, K.F.,Read, J.,Gu, R.F.,Roth, M.,Toader, D.,Saeh, J.C.,Chen, H.
Mechanism and In Vitro Pharmacology of TAK1 Inhibition by (5Z)-7-Oxozeaenol.
Acs Chem.Biol., 8:643-650, 2013

PubMed Abstract: Transforming growth factor-β activated kinase-1 (TAK1) is a member of the mitogen-activated protein kinase kinase kinase (MAP3K) family that regulates several signaling pathways including NF-κB signal transduction and p38 activation. TAK1 deregulation has been implicated in human diseases including cancer and inflammation. Here, we show that, in addition to its kinase activity, TAK1 has intrinsic ATPase activity, that (5Z)-7-Oxozeaenol irreversibly inhibits TAK1, and that sensitivity to (5Z)-7-Oxozeaenol inhibition in hematological cancer cell lines is NRAS mutation status and TAK1 pathway dependent. X-ray crystallographic and mass spectrometric studies showed that (5Z)-7-Oxozeaenol forms a covalent complex with TAK1. Detailed biochemical characterization revealed that (5Z)-7-Oxozeaenol inhibited both the kinase and the ATPase activity of TAK1 following a bi-phase kinetics, consistent with the irreversible inhibition mechanism. In DoHH2 cells, (5Z)-7-Oxozeaenol potently inhibited the p38 phosphorylation driven by TAK1, and the inhibition lasted over 6 h after withdrawal of (5Z)-7-Oxozeaenol. Profiling (5Z)-7-Oxozeaenol in a panel of hematological cancer cells showed that sensitive cell lines tended to carry NRAS mutations and that genes in TAK1 regulated pathways were enriched in sensitive cell lines. Taken together, we have elucidated the molecular mechanism of a TAK1 irreversible inhibitor and laid the foundation for designing next generation TAK1 irreversible inhibitors. The NRAS-TAK1-Wnt signaling network discerned in our study may prove to be useful in patient selection for TAK1 targeted agents in hematological cancers.

PubMed: 23272696
DOI: 10.1021/cb3005897

実験手法

X-RAY DIFFRACTION (2.2 Å)