8K6Q

Crystal structure of HOIL-1L LTM domain

8K6Q の概要

• エントリーDOI: 10.2210/pdb8k6q/pdb
• 分子名称: RanBP-type and C3HC4-type zinc finger-containing protein 1 (2 entities in total)
• 機能のキーワード: hoil-1l, ltm, structural protein
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 24664.41

構造登録者

Yan, Z.,Pan, L.F. (登録日: 2023-07-25, 公開日: 2024-07-03)

主引用文献

Zhang, Y.,Xu, X.,Wang, Y.,Wang, Y.,Zhou, X.,Pan, L.
Mechanistic insights into the homo-dimerization of HOIL-1L and SHARPIN.
Biochem.Biophys.Res.Commun., 689:149239-149239, 2023

PubMed Abstract: HOIL-1L and SHARPIN are two essential regulatory subunits of the linear ubiquitin chain assembly complex (LUBAC), which is the only known E3 ligase complex generating linear ubiquitin chains. In addition to their LUBAC-dependent functions, HOIL-1L and SHARPIN alone play crucial roles in many LUBAC-independent cellular processes. Importantly, deficiency of HOIL-1L or SHARPIN leads to severe disorders in humans or mice. However, the mechanistic bases underlying the multi-functions of HOIL-1L and SHARPIN are still largely unknown. Here, we uncover that HOIL-1L and SHARPIN alone can form homo-dimers through their LTM motifs. We solve two crystal structures of the dimeric LTM motifs of HOIL-1L and SHARPIN, which not only elucidate the detailed molecular mechanism underpinning the dimer formations of HOIL-1L and SHARPIN, but also reveal a general mode shared by the LTM motifs of HOIL-1L and SHARPIN for forming homo-dimer or hetero-dimer. Furthermore, we elucidate that the polyglucosan body myopathy-associated HOIL-1L A18P mutation disturbs the structural folding of HOIL-1L LTM, and disrupts the dimer formation of HOIL-1L. In summary, our study provides mechanistic insights into the homo-dimerization of HOIL-1L and SHARPIN mediated by their LTM motifs, and expands our understandings of the multi-functions of HOIL-1L and SHARPIN as well as the etiology of relevant human disease caused by defective HOIL-1L.

PubMed: 37976837
DOI: 10.1016/j.bbrc.2023.149239

実験手法

X-RAY DIFFRACTION (1.59 Å)