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6M1K

USP7 in complex with a novel inhibitor

Summary for 6M1K
Entry DOI10.2210/pdb6m1k/pdb
DescriptorUbiquitin carboxyl-terminal hydrolase 7, methyl 4-[[4-[[3-[4-(aminomethyl)phenyl]-2-methyl-7-oxidanylidene-pyrazolo[4,3-d]pyrimidin-6-yl]methyl]-4-oxidanyl-piperidin-1-yl]methyl]-3-chloranyl-benzoate (3 entities in total)
Functional Keywordsinhibitor, complex, usp7, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight81450.90
Authors
Liu, S.J.,Zhou, X.Y.,Li, M.L.,Sun, H.B.,Wen, X.A. (deposition date: 2020-02-26, release date: 2021-03-10, Last modification date: 2023-11-29)
Primary citationLi, M.,Liu, S.,Chen, H.,Zhou, X.,Zhou, J.,Zhou, S.,Yuan, H.,Xu, Q.L.,Liu, J.,Cheng, K.,Sun, H.,Wang, Y.,Chen, C.,Wen, X.
N-benzylpiperidinol derivatives as novel USP7 inhibitors: Structure-activity relationships and X-ray crystallographic studies.
Eur.J.Med.Chem., 199:112279-112279, 2020
Cited by
PubMed: 32497973
DOI: 10.1016/j.ejmech.2020.112279
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.255 Å)
Structure validation

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