4ZGI

Structure of Truncated Human TIFA

4ZGI の概要

• エントリーDOI: 10.2210/pdb4zgi/pdb
• 関連するPDBエントリー: 4YM4
• 分子名称: TRAF-interacting protein with FHA domain-containing protein A (2 entities in total)
• 機能のキーワード: fha domian, adaptor, signaling protein
• 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: 16720.40

構造登録者

Weng, J.H.,Wei, T.Y.W.,Hsieh, Y.C.,Huang, C.C.F.,Wu, P.Y.G.,Chen, E.S.W.,Huang, K.F.,Chen, C.J.,Tsai, M.D. (登録日: 2015-04-23, 公開日: 2015-10-14, 最終更新日: 2024-10-23)

主引用文献

Weng, J.H.,Hsieh, Y.C.,Huang, C.C.,Wei, T.Y.,Lim, L.H.,Chen, Y.H.,Ho, M.R.,Wang, I.,Huang, K.F.,Chen, C.J.,Tsai, M.D.
Uncovering the Mechanism of Forkhead-Associated Domain-Mediated TIFA Oligomerization That Plays a Central Role in Immune Responses.
Biochemistry, 54:6219-6229, 2015

PubMed Abstract: Forkhead-associated (FHA) domain is the only signaling domain that recognizes phosphothreonine (pThr) specifically. TRAF-interacting protein with an FHA domain (TIFA) was shown to be involved in immune responses by binding with TRAF2 and TRAF6. We recently reported that TIFA is a dimer in solution and that, upon stimulation by TNF-α, TIFA is phosphorylated at Thr9, which triggers TIFA oligomerization via pThr9-FHA domain binding and activates nuclear factor κB (NF-κB). However, the structural mechanism for the functionally important TIFA oligomerization remains to be established. While FHA domain-pThr binding is known to mediate protein dimerization, its role in oligomerization has not been demonstrated at the structural level. Here we report the crystal structures of TIFA (residues 1-150, with the unstructured C-terminal tail truncated) and its complex with the N-terminal pThr9 peptide (residues 1-15), which show unique features in the FHA structure (intrinsic dimer and extra β-strand) and in its interaction with the pThr peptide (with residues preceding rather than following pThr). These structural features support previous and additional functional analyses. Furthermore, the structure of the complex suggests that the pThr9-FHA domain interaction can occur only between different sets of dimers rather than between the two protomers within a dimer, providing the structural mechanism for TIFA oligomerization. Our results uncover the mechanism of FHA domain-mediated oligomerization in a key step of immune responses and expand the paradigm of FHA domain structure and function.

PubMed: 26389808
DOI: 10.1021/acs.biochem.5b00500

実験手法

X-RAY DIFFRACTION (2.701 Å)