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PDBsum entry 6sio

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Top Page protein ligands metals Protein-protein interface(s) links
Peptide binding protein PDB id
6sio
Contents
Protein chains
225 a.a.
12 a.a.
Ligands
LFQ ×2
Metals
_MG ×2
_CL
Waters ×355

References listed in PDB file
Key reference
Title Fragment-Based differential targeting of ppi stabilizer interfaces.
Authors X.Guillory, M.Wolter, S.Leysen, J.F.Neves, A.Kuusk, S.Genet, B.Somsen, J.K.Morrow, E.Rivers, L.Van beek, J.Patel, R.Goodnow, H.Schoenherr, N.Fuller, Q.Cao, R.G.Doveston, L.Brunsveld, M.R.Arkin, P.Castaldi, H.Boyd, I.Landrieu, H.Chen, C.Ottmann.
Ref. J Med Chem, 2020, 63, 6694-6707. [DOI no: 10.1021/acs.jmedchem.9b01942]
PubMed id 32501690
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.
PROCHECK
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 Headers

 

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