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-Structure paper
Title | Discovery of Potent, Selective, and Orally Bioavailable Inhibitors of USP7 with In Vivo Antitumor Activity. |
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Journal, issue, pages | J. Med. Chem., Vol. 63, Page 5398-5420, Year 2020 |
Publish date | Jan 29, 2020 (structure data deposition date) |
Authors | Leger, P.R. / Hu, D.X. / Biannic, B. / Bui, M. / Han, X. / Karbarz, E. / Maung, J. / Okano, A. / Osipov, M. / Shibuya, G.M. ...Leger, P.R. / Hu, D.X. / Biannic, B. / Bui, M. / Han, X. / Karbarz, E. / Maung, J. / Okano, A. / Osipov, M. / Shibuya, G.M. / Young, K. / Higgs, C. / Abraham, B. / Bradford, D. / Cho, C. / Colas, C. / Jacobson, S. / Ohol, Y.M. / Pookot, D. / Rana, P. / Sanchez, J. / Shah, N. / Sun, M. / Wong, S. / Brockstedt, D.G. / Kassner, P.D. / Schwarz, J.B. / Wustrow, D.J. |
External links | J. Med. Chem. / PubMed:32302140 |
Methods | X-ray diffraction |
Resolution | 2.69 - 2.99 Å |
Structure data | PDB-6vn2: PDB-6vn3: PDB-6vn4: PDB-6vn5: PDB-6vn6: |
Chemicals | ChemComp-R44: ChemComp-ACT: ChemComp-HOH: ChemComp-R3Y: ChemComp-R4D: ChemComp-R41: ChemComp-R4J: ChemComp-ZN: |
Source |
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Keywords | HYDROLASE / USP7 / DUB / DEUBIQUITINASE |