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Medchemcomm|January 28, 2014
The structure-activity relationships of L3MBTL3 inhibitors: flexibility of the dimer interfaceMichelle A Camerino, Nan Zhong, Aiping Dong, et al.
Communications Biology|December 16, 2023
The co-crystal structure of Cbl-b and a small-molecule inhibitor reveals the mechanism of Cbl-b inhibitionSerah W Kimani, Sumera Perveen, Magdalena Szewezyk, et al.
The Journal of Biological Chemistry|May 7, 2003
Integrating structure, bioinformatics, and enzymology to discover function: BioH, a new carboxylesterase from Escherichia coliRuslan Sanishvili, Alexander F Yakunin, Roman A Laskowski, et al.
Journal of Medicinal Chemistry|September 18, 2013
Small-molecule ligands of methyl-lysine binding proteins: optimization of selectivity for L3MBTL3Lindsey I James, Victoria K Korboukh, Liubov Krichevsky, et al.
Experimental Hematology|December 10, 2023
Epigenetic vulnerabilities of leukemia harboring inactivating EZH2 mutationsMona A Alqazzaz, Genna M Luciani, Victoria Vu, et al.
Journal of Medicinal Chemistry|October 12, 2017
Small Molecule Antagonists of the Interaction between the Histone Deacetylase 6 Zinc-Finger Domain and UbiquitinRachel J Harding, Renato Ferreira de Freitas, Patrick Collins, et al.
Nature Chemical Biology|June 8, 2022
Structure and activity of human TMPRSS2 protease implicated in SARS-CoV-2 activationBryan J Fraser, Serap Beldar, Almagul Seitova, et al.
Nucleic Acids Research|November 22, 2018
Direct interaction between the PRDM3 and PRDM16 tumor suppressors and the NuRD chromatin remodeling complexDanton Ivanochko, Levon Halabelian, Elizabeth Henderson, et al.
Biorxiv : the Preprint Server for Biology|May 22, 2023
SETDB1 Triple Tudor Domain Ligand, ( R,R )-59, Promotes Methylation of Akt1 in CellsMélanie Uguen, Yu Deng, Fengling Li, et al.
Journal of Medicinal Chemistry|November 3, 2016
Structure-Based Design of a Covalent Inhibitor of the SET Domain-Containing Protein 8 (SETD8) Lysine MethyltransferaseKyle V Butler, Anqi Ma, Wenyu Yu, et al.
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