7T8F

G93A mutant of human SOD1 bound with Ebselen in P21 space group

7T8F の概要

• エントリーDOI: 10.2210/pdb7t8f/pdb
• 分子名称: Superoxide dismutase [Cu-Zn], ZINC ION, ACETATE ION, ... (5 entities in total)
• 機能のキーワード: sod1, als, drug discovery, oxidoreductase
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 32556.24

構造登録者

Amporndanai, K.,Hasnain, S.S. (登録日: 2021-12-16, 公開日: 2023-01-25, 最終更新日: 2024-06-05)

主引用文献

Watanabe, S.,Amporndanai, K.,Awais, R.,Latham, C.,Awais, M.,O'Neill, P.M.,Yamanaka, K.,Hasnain, S.S.
Ebselen analogues delay disease onset and its course in fALS by on-target SOD-1 engagement.
Sci Rep, 14:12118-12118, 2024

PubMed Abstract: Amyotrophic lateral sclerosis (ALS) selectively affects motor neurons. SOD1 is the first causative gene to be identified for ALS and accounts for at least 20% of the familial (fALS) and up to 4% of sporadic (sALS) cases globally with some geographical variability. The destabilisation of the SOD1 dimer is a key driving force in fALS and sALS. Protein aggregation resulting from the destabilised SOD1 is arrested by the clinical drug ebselen and its analogues (MR6-8-2 and MR6-26-2) by redeeming the stability of the SOD1 dimer. The in vitro target engagement of these compounds is demonstrated using the bimolecular fluorescence complementation assay with protein-ligand binding directly visualised by co-crystallography in G93A SOD1. MR6-26-2 offers neuroprotection slowing disease onset of SOD1 mice by approximately 15 days. It also protected neuromuscular junction from muscle denervation in SOD1 mice clearly indicating functional improvement.

PubMed: 38802492
DOI: 10.1038/s41598-024-62903-5

実験手法

X-RAY DIFFRACTION (1.4 Å)