Dynamic Protein Acylation: New Substrates, Mechanisms, and Drug Targets von Lanyon-Hogg, Thomas, Faronato, Monica, Serwa, Remigiusz A., Tate, Edward W.

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UCHL1 as a novel target in breast cancer: emerging insights from cell and chemical biology von Mondal, Milon, Conole, Daniel, Nautiyal, Jaya, Tate, Edward W.

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Antibody-PROTAC Conjugates Enable HER2-Dependent Targeted Protein Degradation of BRD4 von Maneiro, Maria, Forte, Nafsika, Shchepinova, Maria M., Kounde, Cyrille S., Chudasama, Vijay, Baker, James Richard, Tate, Edward W.

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A caged E3 ligase ligand for PROTAC-mediated protein degradation with light von Kounde, Cyrille S, Shchepinova, Maria M, Saunders, Charlie N, Muelbaier, Marcel, Rackham, Mark D, Harling, John D, Tate, Edward W

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Bacterial enzymes: powerful tools for protein labeling, cell signaling, and therapeutic discovery von Liu, Lu, Gray, Janine L., Tate, Edward W., Yang, Aimin

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Protein lipidation in cancer: mechanisms, dysregulation and emerging drug targets von Tate, Edward W., Soday, Lior, de la Lastra, Ana Losada, Wang, Mei, Lin, Hening

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Inhibition of vaccinia virus L1 N-myristoylation by the host N-myristoyltransferase inhibitor IMP-1088 generates non-infectious virions defective in cell entry von Priyamvada, Lalita, Kallemeijn, Wouter W, Faronato, Monica, Wilkins, Kimberly, Goldsmith, Cynthia S, Cotter, Catherine A, Ojeda, Suany, Solari, Roberto, Moss, Bernard, Tate, Edward W, Satheshkumar, Panayampalli Subbian

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Global profiling of co- and post-translationally N-myristoylated proteomes in human cells von Thinon, Emmanuelle, Serwa, Remigiusz A., Broncel, Malgorzata, Brannigan, James A., Brassat, Ute, Wright, Megan H., Heal, William P., Wilkinson, Anthony J., Mann, David J., Tate, Edward W.

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Targeting methionine aminopeptidase 2 in cancer, obesity, and autoimmunity von Goya Grocin, Andrea, Kallemeijn, Wouter W., Tate, Edward W.

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High-resolution snapshots of human N-myristoyltransferase in action illuminate a mechanism promoting N-terminal Lys and Gly myristoylation von Dian, Cyril, Pérez-Dorado, Inmaculada, Rivière, Frédéric, Asensio, Thomas, Legrand, Pierre, Ritzefeld, Markus, Shen, Mengjie, Cota, Ernesto, Meinnel, Thierry, Tate, Edward W., Giglione, Carmela

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Weaponizing the proteasome to overcome antimalarial drug resistance von Xiao, Zhangping, Gray, Janine L., Tate, Edward W.

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Photoactive Bifunctional Degraders: Precision Tools To Regulate Protein Stability von Kounde, Cyrille S., Tate, Edward W.

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Global profiling of protein lipidation using chemical proteomic technologies von Tate, Edward W, Kalesh, Karunakaran A, Lanyon-Hogg, Thomas, Storck, Elisabeth M, Thinon, Emmanuelle

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Discovery of lipid-mediated protein-protein interactions in living cells using metabolic labeling with photoactivatable clickable probes von Fedoryshchak, Roman O, Gorelik, Andrii, Shen, Mengjie, Shchepinova, Maria M, Pérez-Dorado, Inmaculada, Tate, Edward W

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A Natural Product Puts Malaria on a Low-Fat Diet von Lucy, Daniel, Zhang, Leran, Tate, Edward W.

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Structural basis for membrane attack complex inhibition by CD59 von Couves, Emma C., Gardner, Scott, Voisin, Tomas B., Bickel, Jasmine K., Stansfeld, Phillip J., Tate, Edward W., Bubeck, Doryen

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Activity-based probes: discovering new biology and new drug targets von Heal, William P, Dang, T. H. Tam, Tate, Edward W

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Deconvoluting the biology and druggability of protein lipidation using chemical proteomics von Losada de la Lastra, Ana, Hassan, Sarah, Tate, Edward W.

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Evaluating Hedgehog Acyltransferase Activity and Inhibition Using the Acylation-coupled Lipophilic Induction of Polarization (Acyl-cLIP) Assay von Andrei, Sebastian A., Tate, Edward W., Lanyon-Hogg, Thomas

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Discovery of a Potent and Selective Covalent Inhibitor and Activity-Based Probe for the Deubiquitylating Enzyme UCHL1, with Antifibrotic Activity von Panyain, Nattawadee, Godinat, Aurélien, Lanyon-Hogg, Thomas, Lachiondo-Ortega, Sofía, Will, Edward J, Soudy, Christelle, Mondal, Milon, Mason, Katie, Elkhalifa, Sarah, Smith, Lisa M, Harrigan, Jeanine A, Tate, Edward W

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