7YUJ

Crystal structure of HOIL-1L(365-510)

Summary for 7YUJ

• Entry DOI: 10.2210/pdb7yuj/pdb
• Descriptor: RanBP-type and C3HC4-type zinc finger-containing protein 1, ZINC ION, DI(HYDROXYETHYL)ETHER, ... (4 entities in total)
• Functional Keywords: e3, ubiquitination, rbr, ligase
• Biological source: Homo sapiens (human)
• Total number of polymer chains: 2
• Total formula weight: 34330.76

Authors

Xiao, L.,Pan, L. (deposition date: 2022-08-17, release date: 2023-08-30, Last modification date: 2024-03-13)

Primary citation

Xu, X.,Wang, Y.,Zhang, Y.,Wang, Y.,Yin, Y.,Peng, C.,Gong, X.,Li, M.,Zhang, Y.,Zhang, M.,Tang, Y.,Zhou, X.,Liu, H.,Pan, L.
Mechanistic insights into the enzymatic activity of E3 ligase HOIL-1L and its regulation by the linear ubiquitin chain binding.
Sci Adv, 9:eadi4599-eadi4599, 2023

PubMed Abstract: Heme-oxidized IRP2 ubiquitin ligase 1 (HOIL-1L) serves as a unique E3 ligase to catalyze the mono-ubiquitination of relevant protein or sugar substrates and plays vital roles in numerous cellular processes in mammals. However, the molecular mechanism underpinning the E3 activity of HOIL-1L and the related regulatory mechanism remain elusive. Here, we report the crystal structure of the catalytic core region of HOIL-1L and unveil the key catalytic triad residues of HOIL-1L. Moreover, we discover that HOIL-1L contains two distinct linear di-ubiquitin binding sites that can synergistically bind to linear tetra-ubiquitin, and the binding of HOIL-1L with linear tetra-ubiquitin can promote its E3 activity. The determined HOIL-1L/linear tetra-ubiquitin complex structure not only elucidates the detailed binding mechanism of HOIL-1L with linear tetra-ubiquitin but also uncovers a unique allosteric ubiquitin-binding site for the activation of HOIL-1L. In all, our findings provide mechanistic insights into the E3 activity of HOIL-1L and its regulation by the linear ubiquitin chain binding.

PubMed: 37831767
DOI: 10.1126/sciadv.adi4599

Experimental method

X-RAY DIFFRACTION (1.865 Å)