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6S64

Crystal structure of hTEAD2 in complex with a trisubstituted pyrazole inhibitor

Summary for 6S64
Entry DOI10.2210/pdb6s64/pdb
Related6S60
DescriptorTranscriptional enhancer factor TEF-4, MYRISTIC ACID, PALMITIC ACID, ... (5 entities in total)
Functional Keywordstead2, inhibitor, transcription
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight55881.26
Authors
Sturbaut, M.,Allemand, F.,Guichou, J.F. (deposition date: 2019-07-02, release date: 2020-07-22, Last modification date: 2024-11-06)
Primary citationSturbaut, M.,Bailly, F.,Coevoet, M.,Sileo, P.,Pugniere, M.,Liberelle, M.,Magnez, R.,Thuru, X.,Chartier-Harlin, M.C.,Melnyk, P.,Gelin, M.,Allemand, F.,Guichou, J.F.,Cotelle, P.
Discovery of a cryptic site at the interface 2 of TEAD - Towards a new family of YAP/TAZ-TEAD inhibitors.
Eur.J.Med.Chem., 226:113835-113835, 2021
Cited by
PubMed Abstract: The Hippo pathway is involved in organ size control and tissue homeostasis by regulating cell growth, proliferation and apoptosis. It controls the phosphorylation of the transcription co-activator YAP (Yes associated protein) and TAZ (Transcriptional coactivator with PDZ-binding motif) in order to control their nuclear import and their interaction with TEAD (Transcriptional Enhanced Associated Domain). YAP, TAZ and TEADs are dysregulated in several cancers making YAP/TAZ-TEAD interaction a new emerging anti-cancer target. We report the synthesis of a set of trisubstituted pyrazoles which bind to hTEAD2 at the interface 2 revealing for the first time a cryptic pocket created by the movement of the phenol ring of Y382. Compound 6 disrupts YAP/TAZ-TEAD interaction in HEK293T cells and inhibits TEAD target genes and cell proliferation in MDA-MB-231 cells. Compound 6 is therefore the first inhibitor of YAP/TAZ-TEAD targeting interface 2. This molecule could serve with other pan-TEAD inhibitors such as interface 3 ligands, for the delineation of the relative importance of VGLL vs YAP/TAZ in a given cellular model.
PubMed: 34509860
DOI: 10.1016/j.ejmech.2021.113835
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.22 Å)
Structure validation

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