Search Results - "Tate, Edward W."

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

    “…Post-translational attachment of lipids to proteins is found in all organisms, and is important for many biological processes. Acylation with myristic and…”
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    Global profiling of co- and post-translationally N-myristoylated proteomes in human cells by 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.

    Published in Nature communications (26-09-2014)
    “…Protein N -myristoylation is a ubiquitous co- and post-translational modification that has been implicated in the development and progression of a range of…”
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    High-resolution snapshots of human N-myristoyltransferase in action illuminate a mechanism promoting N-terminal Lys and Gly myristoylation by Dian, Cyril, Pérez-Dorado, Inmaculada, Rivière, Frédéric, Asensio, Thomas, Legrand, Pierre, Ritzefeld, Markus, Shen, Mengjie, Cota, Ernesto, Meinnel, Thierry, Tate, Edward W., Giglione, Carmela

    Published in Nature communications (28-02-2020)
    “…The promising drug target N -myristoyltransferase (NMT) catalyses an essential protein modification thought to occur exclusively at N-terminal glycines (Gly)…”
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    Global profiling of protein lipidation using chemical proteomic technologies by Tate, Edward W, Kalesh, Karunakaran A, Lanyon-Hogg, Thomas, Storck, Elisabeth M, Thinon, Emmanuelle

    Published in Current opinion in chemical biology (01-02-2015)
    “…•Protein lipidation is an essential modification (PTM) in all forms of life.•Key modifications include acylation, prenylation, cholesterylation and GPI…”
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    Structural basis for membrane attack complex inhibition by CD59 by Couves, Emma C., Gardner, Scott, Voisin, Tomas B., Bickel, Jasmine K., Stansfeld, Phillip J., Tate, Edward W., Bubeck, Doryen

    Published in Nature communications (16-02-2023)
    “…CD59 is an abundant immuno-regulatory receptor that protects human cells from damage during complement activation. Here we show how the receptor binds…”
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    Activity-based probes: discovering new biology and new drug targets by Heal, William P, Dang, T H Tam, Tate, Edward W

    Published in Chemical Society reviews (01-01-2011)
    “…The development and application of chemical technologies enabling direct analysis of enzyme activity in living systems has undergone explosive growth in recent…”
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    Discovery of lipid-mediated protein-protein interactions in living cells using metabolic labeling with photoactivatable clickable probes by Fedoryshchak, Roman O, Gorelik, Andrii, Shen, Mengjie, Shchepinova, Maria M, Pérez-Dorado, Inmaculada, Tate, Edward W

    Published in Chemical science (Cambridge) (01-03-2023)
    “…Protein-protein interactions (PPIs) are essential and pervasive regulatory elements in biology. Despite the development of a range of techniques to probe PPIs…”
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    High‐Throughput Kinetic Analysis for Target‐Directed Covalent Ligand Discovery by Craven, Gregory B., Affron, Dominic P., Allen, Charlotte E., Matthies, Stefan, Greener, Joe G., Morgan, Rhodri M. L., Tate, Edward W., Armstrong, Alan, Mann, David J.

    Published in Angewandte Chemie International Edition (04-05-2018)
    “…Cysteine‐reactive small molecules are used as chemical probes of biological systems and as medicines. Identifying high‐quality covalent ligands requires…”
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    Validation and Invalidation of Chemical Probes for the Human N-myristoyltransferases by Kallemeijn, Wouter W, Lueg, Gregor A, Faronato, Monica, Hadavizadeh, Kate, Goya Grocin, Andrea, Song, Ok-Ryul, Howell, Michael, Calado, Dinis P, Tate, Edward W

    Published in Cell chemical biology (20-06-2019)
    “…On-target, cell-active chemical probes are of fundamental importance in chemical and cell biology, whereas poorly characterized probes often lead to invalid…”
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    d-Cycloserine destruction by alanine racemase and the limit of irreversible inhibition by de Chiara, Cesira, Homšak, Miha, Prosser, Gareth A., Douglas, Holly L., Garza-Garcia, Acely, Kelly, Geoff, Purkiss, Andrew G., Tate, Edward W., de Carvalho, Luiz Pedro S.

    Published in Nature chemical biology (01-06-2020)
    “…The broad-spectrum antibiotic d -cycloserine (DCS) is a key component of regimens used to treat multi- and extensively drug-resistant tuberculosis. DCS, a…”
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    Building bridges for highly selective, potent and stable oxytocin and vasopressin analogs by Beard, Rhiannon, Stucki, Andy, Schmitt, Muriel, Py, Gabrielle, Grundschober, Christophe, Gee, Antony D., Tate, Edward W.

    Published in Bioorganic & medicinal chemistry (15-07-2018)
    “…[Display omitted] •Unique SAR discovered for xylene-bridged oxytocin peptide analogs.•Affinity, selectivity and potency influenced by bridging distance.•Meta…”
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    Multifunctional protein labeling via enzymatic N-terminal tagging and elaboration by click chemistry by Heal, William P, Wright, Megan H, Thinon, Emmanuelle, Tate, Edward W

    Published in Nature protocols (01-01-2012)
    “…A protocol for selective and site-specific enzymatic labeling of proteins is described. The method exploits the protein co-/post-translational modification…”
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    Target profiling of zerumbone using a novel cell-permeable clickable probe and quantitative chemical proteomics by Kalesh, Karunakaran A, Clulow, James A, Tate, Edward W

    “…Zerumbone is a phytochemical with diverse biological activities ranging from anti-inflammatory to anti-cancer properties; however, to date the cellular targets…”
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    Dynamics and Molecular Interactions of GPI-Anchored CD59 by Voisin, Tomas B, Couves, Emma C, Tate, Edward W, Bubeck, Doryen

    Published in Toxins (30-06-2023)
    “…CD59 is a GPI-anchored cell surface receptor that serves as a gatekeeper to controlling pore formation. It is the only membrane-bound inhibitor of the…”
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