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6RJQ

Fragment AZ-006 binding at the TAZpS89/14-3-3 sigma interface

Summary for 6RJQ
Entry DOI10.2210/pdb6rjq/pdb
Descriptor14-3-3 protein sigma, TAZpS89, 4-[[(2~{S})-1-azanylpropan-2-yl]amino]-6-(sulfanylmethyl)-1-benzothiophene-2-carboximidamide, ... (4 entities in total)
Functional Keywordsprotein protein interaction, fragment soaking, stabilization, peptide binding protein
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains2
Total formula weight30221.83
Authors
Genet, S.,Wolter, M.,Guillory, X.,Somsen, B.,Leysen, S.,Castaldi, P.,Ottmann, C.,Patel, J. (deposition date: 2019-04-29, release date: 2020-06-17, Last modification date: 2024-10-23)
Primary citationGuillory, X.,Wolter, M.,Leysen, S.,Neves, J.F.,Kuusk, A.,Genet, S.,Somsen, B.,Morrow, J.K.,Rivers, E.,van Beek, L.,Patel, J.,Goodnow, R.,Schoenherr, H.,Fuller, N.,Cao, Q.,Doveston, R.G.,Brunsveld, L.,Arkin, M.R.,Castaldi, P.,Boyd, H.,Landrieu, I.,Chen, H.,Ottmann, C.
Fragment-based Differential Targeting of PPI Stabilizer Interfaces.
J.Med.Chem., 63:6694-6707, 2020
Cited by
PubMed Abstract: Stabilization of protein-protein interactions (PPIs) holds great potential for therapeutic agents, as illustrated by the successful drugs rapamycin and lenalidomide. However, how such interface-binding molecules can be created in a rational, bottom-up manner is a largely unanswered question. We report here how a fragment-based approach can be used to identify chemical starting points for the development of small-molecule stabilizers that differentiate between two different PPI interfaces of the adapter protein 14-3-3. The fragments discriminately bind to the interface of 14-3-3 with the recognition motif of either the tumor suppressor protein p53 or the oncogenic transcription factor TAZ. This X-ray crystallography driven study shows that the rim of the interface of individual 14-3-3 complexes can be targeted in a differential manner with fragments that represent promising starting points for the development of specific 14-3-3 PPI stabilizers.
PubMed: 32501690
DOI: 10.1021/acs.jmedchem.9b01942
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.885 Å)
Structure validation

226707

건을2024-10-30부터공개중

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