9PQA

Fem-1 homolog B (FEM1B) in complex with VU0432623

これはPDB形式変換不可エントリーです。

9PQA の概要

• エントリーDOI: 10.2210/pdb9pqa/pdb
• 分子名称: Protein fem-1 homolog B, (6R)-6-phenyl-1,3-thiazinane-2,4-dione, SULFATE ION, ... (4 entities in total)
• 機能のキーワード: fem1b, ligand, e3 ligase, ligase
• 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: 79486.43

構造登録者

Katinas, J.M.,Fesik, S.W. (登録日: 2025-07-22, 公開日: 2025-11-26)

主引用文献

Katinas, J.M.,Amporndanai, K.,Taylor, A.J.,Rose, K.L.,Gareiss, P.C.,Crespo, R.A.,Phan, J.,Waterson, A.G.,Fesik, S.W.
Nuclear Magnetic Resonance-based fragment screen of the E3 ligase Fem-1 homolog B.
Protein Sci., 34:e70365-e70365, 2025

PubMed Abstract: Targeted protein degradation using PROTACs (PROteolysis TArgeting Chimeras) has emerged as a transformative therapeutic strategy, largely relying on a small number of E3 ubiquitin ligases such as CRBN and VHL. However, resistance, toxicity, and poor oral bioavailability limit the utility of PROTACs and highlight the need to expand the E3 ligase toolbox. Fem-1 homolog B (FEM1B) is a lesser-known E3 ligase that offers a promising alternative due to its broad expression and ability to recognize diverse degron motifs. Here, we describe the development of a stable construct of FEM1B, the results of a protein-observed NMR-based fragment screen using this construct, and the X-ray structures of some of the fragment hits when bound to the protein. From these results, new PROTACs utilizing FEM1B as the E3 ligase may be discovered, providing an alternative E3 ligase for targeted protein degradation.

PubMed: 41229306
DOI: 10.1002/pro.70365

実験手法

X-RAY DIFFRACTION (2.9 Å)