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6VYC

Crystal structure of WD-repeat domain of human WDR91

6VYC の概要
エントリーDOI10.2210/pdb6vyc/pdb
分子名称WD repeat-containing protein 91, UNKNOWN ATOM OR ION (3 entities in total)
機能のキーワードwdr91, wd-repeat, structural genomics, structural genomics consortium, sgc, protein transport
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82128.95
構造登録者
Halabelian, L.,Hutchinson, A.,Li, Y.,Seitova, A.,Bountra, C.,Edwards, A.M.,Arrowsmith, C.H.,Structural Genomics Consortium (SGC) (登録日: 2020-02-26, 公開日: 2020-03-25, 最終更新日: 2024-05-01)
主引用文献Ahmad, S.,Xu, J.,Feng, J.A.,Hutchinson, A.,Zeng, H.,Ghiabi, P.,Dong, A.,Centrella, P.A.,Clark, M.A.,Guie, M.A.,Guilinger, J.P.,Keefe, A.D.,Zhang, Y.,Cerruti, T.,Cuozzo, J.W.,von Rechenberg, M.,Bolotokova, A.,Li, Y.,Loppnau, P.,Seitova, A.,Li, Y.Y.,Santhakumar, V.,Brown, P.J.,Ackloo, S.,Halabelian, L.
Discovery of a First-in-Class Small-Molecule Ligand for WDR91 Using DNA-Encoded Chemical Library Selection Followed by Machine Learning.
J.Med.Chem., 66:16051-16061, 2023
Cited by
PubMed Abstract: WD40 repeat-containing protein 91 (WDR91) regulates early-to-late endosome conversion and plays vital roles in endosome fusion, recycling, and transport. WDR91 was recently identified as a potential host factor for viral infection. We employed DNA-encoded chemical library (DEL) selection against the WDR domain of WDR91, followed by machine learning to predict ligands from the synthetically accessible Enamine REAL database. Screening of predicted compounds identified a WDR91 selective compound , with a of 6 ± 2 μM by surface plasmon resonance. The co-crystal structure confirmed the binding of to the WDR91 side pocket, in proximity to cysteine 487, which led to the discovery of covalent analogues and . The covalent adduct formation for and was confirmed by intact mass liquid chromatography-mass spectrometry. The discovery of , , and , accompanying structure-activity relationship, and the co-crystal structures provide valuable insights for designing potent and selective chemical tools against WDR91 to evaluate its therapeutic potential.
PubMed: 37996079
DOI: 10.1021/acs.jmedchem.3c01471
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.1 Å)
構造検証レポート
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件を2025-06-18に公開中

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