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9RUS

Structure of WRN in complex with ATPgS and Compound 3

Summary for 9RUS
Entry DOI10.2210/pdb9rus/pdb
Related9RTI
DescriptorBifunctional 3'-5' exonuclease/ATP-dependent helicase WRN, PHOSPHOTHIOPHOSPHORIC ACID-ADENYLATE ESTER, 1-[(4-fluorophenyl)methyl]benzimidazole, ... (9 entities in total)
Functional Keywordsdna damage repair, inhibitor, complex, helicase, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight99896.98
Authors
Fletcher, C.T.,Rucktooa, P. (deposition date: 2025-07-04, release date: 2025-10-22, Last modification date: 2025-11-05)
Primary citationSmith, G.M.T.,Aithani, L.,Barrett, C.E.,Bucher, A.O.,Cooper, C.D.O.,Degorce, S.L.,Dore, A.S.,Fletcher, C.T.,Huber, S.,Huckvale, R.,Kennedy, A.J.,Mornement, A.A.,Pickworth, M.,Rucktooa, P.,Scully, C.C.G.,Skerratt, S.E.
AI-assisted delivery of novel covalent WRN inhibitors from a non-covalent fragment screen.
Bioorg.Med.Chem.Lett., 131:130421-130421, 2025
Cited by
PubMed Abstract: Werner (WRN) helicase, has emerged as a promising therapeutic target for cancers associated with microsatellite instability (MSI). This letter describes the discovery of small molecule inhibitors from a fragment screen that occupy a cryptic, allosteric site of WRN helicase. Key findings include the identification of benzimidazole and amino-indazole scaffolds, exploiting their proximity to Cys727 via covalent modification. The use of our proprietary co-folding model DragonFold assisted the identification of novel WRN helicase inhibitors. These, together with near-neighbor profiling, offer tools for furthering the understanding of WRN and BLM helicase function, and potential therapeutic avenues for MSI-associated cancers.
PubMed: 41038585
DOI: 10.1016/j.bmcl.2025.130421
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.193 Å)
Structure validation

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