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6XF3

Crystal structure of STING in complex with E7766

Summary for 6XF3
Entry DOI10.2210/pdb6xf3/pdb
DescriptorStimulator of interferon genes protein, (1R,3R,15E,28R,29R,30R,31R,34R,36R,39S,41R)-29,41-difluoro-34,39-disulfanyl-2,33,35,38,40,42-hexaoxa-4,6,9,11,13,18,20,22,25,27-decaaza-34,39-diphosphaoctacyclo[28.6.4.1~3,36~.1~28,31~.0~4,8~.0~7,12~.0~19,24~.0~23,27~]dotetraconta-5,7,9,11,15,19,21,23,25-nonaene 34,39-dioxide (non-preferred name) (3 entities in total)
Functional Keywordsstimulator of interferon genes (sting), e7766, agonist, macrocycle, immune system
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight43947.11
Authors
Chen, Y.,Wang, J.Y.,Kim, D.-S. (deposition date: 2020-06-15, release date: 2021-02-17, Last modification date: 2023-10-18)
Primary citationKim, D.S.,Endo, A.,Fang, F.G.,Huang, K.C.,Bao, X.,Choi, H.W.,Majumder, U.,Shen, Y.Y.,Mathieu, S.,Zhu, X.,Sanders, K.,Noland, T.,Hao, M.H.,Chen, Y.,Wang, J.Y.,Yasui, S.,TenDyke, K.,Wu, J.,Ingersoll, C.,Loiacono, K.A.,Hutz, J.E.,Sarwar, N.
E7766, a Macrocycle-Bridged Stimulator of Interferon Genes (STING) Agonist with Potent Pan-Genotypic Activity.
Chemmedchem, 16:1740-1743, 2021
Cited by
PubMed Abstract: A strategy for creating potent and pan-genotypic stimulator of interferon genes (STING) agonists is described. Locking a bioactive U-shaped conformation of cyclic dinucleotides by introducing a transannular macrocyclic bridge between the nucleic acid bases leads to a topologically novel macrocycle-bridged STING agonist (MBSA). In addition to substantially enhanced potency, the newly designed MBSAs, exemplified by clinical candidate E7766, exhibit broad pan-genotypic activity in all major human STING variants. E7766 is shown to have potent antitumor activity with long lasting immune memory response in a mouse liver metastatic tumor model. Two complementary stereoselective synthetic routes to E7766 are also described.
PubMed: 33522135
DOI: 10.1002/cmdc.202100068
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.38 Å)
Structure validation

226707

數據於2024-10-30公開中

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