7OMF

Structure of a minimal SF3B core in complex with sudemycin D6 (form I)

7OMF の概要

• エントリーDOI: 10.2210/pdb7omf/pdb
• 関連するPDBエントリー: 5IFE 6EN4 7B0I 7B92 7B9C 7B9I
• 分子名称: Splicing factor 3B subunit 3, Splicing factor 3B subunit 5, Splicing factor 3B subunit 1, ... (7 entities in total)
• 機能のキーワード: splicing inhibitor, sf3b complex, sudemycin d6, splicing
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 219888.70

構造登録者

Cretu, C.,Pena, V. (登録日: 2021-05-21, 公開日: 2021-08-04, 最終更新日: 2024-10-09)

主引用文献

Cretu, C.,Gee, P.,Liu, X.,Agrawal, A.,Nguyen, T.V.,Ghosh, A.K.,Cook, A.,Jurica, M.,Larsen, N.A.,Pena, V.
Structural basis of intron selection by U2 snRNP in the presence of covalent inhibitors.
Nat Commun, 12:4491-4491, 2021

PubMed Abstract: Intron selection during the formation of prespliceosomes is a critical event in pre-mRNA splicing. Chemical modulation of intron selection has emerged as a route for cancer therapy. Splicing modulators alter the splicing patterns in cells by binding to the U2 snRNP (small nuclear ribonucleoprotein)-a complex chaperoning the selection of branch and 3' splice sites. Here we report crystal structures of the SF3B module of the U2 snRNP in complex with spliceostatin and sudemycin FR901464 analogs, and the cryo-electron microscopy structure of a cross-exon prespliceosome-like complex arrested with spliceostatin A. The structures reveal how modulators inactivate the branch site in a sequence-dependent manner and stall an E-to-A prespliceosome intermediate by covalent coupling to a nucleophilic zinc finger belonging to the SF3B subunit PHF5A. These findings support a mechanism of intron recognition by the U2 snRNP as a toehold-mediated strand invasion and advance an unanticipated drug targeting concept.

PubMed: 34301950
DOI: 10.1038/s41467-021-24741-1

実験手法

X-RAY DIFFRACTION (3 Å)