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7Z6L

Crystal structure of PROTAC 5 in complex with the bromodomain of human SMARCA2 and pVHL:ElonginC:ElonginB

Summary for 7Z6L
Entry DOI10.2210/pdb7z6l/pdb
DescriptorProbable global transcription activator SNF2L2, von Hippel-Lindau disease tumor suppressor, Elongin-C, ... (6 entities in total)
Functional Keywordsbromodomain, protac complex, e3 ligase, ligase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains4
Total formula weight56843.93
Authors
Roy, M.J.,Bader, G.,Farnaby, W.,Ciulli, A. (deposition date: 2022-03-12, release date: 2022-09-07, Last modification date: 2024-01-31)
Primary citationKofink, C.,Trainor, N.,Mair, B.,Wohrle, S.,Wurm, M.,Mischerikow, N.,Roy, M.J.,Bader, G.,Greb, P.,Garavel, G.,Diers, E.,McLennan, R.,Whitworth, C.,Vetma, V.,Rumpel, K.,Scharnweber, M.,Fuchs, J.E.,Gerstberger, T.,Cui, Y.,Gremel, G.,Chetta, P.,Hopf, S.,Budano, N.,Rinnenthal, J.,Gmaschitz, G.,Mayer, M.,Koegl, M.,Ciulli, A.,Weinstabl, H.,Farnaby, W.
A selective and orally bioavailable VHL-recruiting PROTAC achieves SMARCA2 degradation in vivo.
Nat Commun, 13:5969-5969, 2022
Cited by
PubMed: 36216795
DOI: 10.1038/s41467-022-33430-6
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.24 Å)
Structure validation

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