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Sergey A. Kozmin grad student 2006 Chicago
 (Bistramide A: From practical chemical synthesis to identification of the cellular receptor.)
Kevan Michael Shokat post-doc 2006-2009 UCSF
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Publications

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Chuong P, Statsyuk A. (2023) Selective Smurf1 E3 ligase inhibitors that prevent transthiolation. Biorxiv : the Preprint Server For Biology
Olp MD, Sprague DJ, Goetz CJ, et al. (2020) Covalent-fragment screening of BRD4 identifies a ligandable site orthogonal to the acetyl-lysine binding sites. Acs Chemical Biology
Kathman SG, Statsyuk AV. (2019) Methodology for Identification of Cysteine-Reactive Covalent Inhibitors. Methods in Molecular Biology (Clifton, N.J.). 1967: 245-262
Chowdhury SR, Kennedy S, Zhu K, et al. (2018) Discovery of covalent enzyme inhibitors using virtual docking of covalent fragments. Bioorganic & Medicinal Chemistry Letters
Foote PK, Statsyuk AV. (2018) Monitoring PARKIN RBR Ubiquitin Ligase Activation States with UbFluor. Current Protocols in Chemical Biology. e45
Ramirez YA, Adler T, Altmann E, et al. (2018) Structural basis of substrate recognition and covalent inhibition of Cdu1 from Chlamydia trachomatis. Chemmedchem
Statsyuk AV. (2018) Let K-Ras activate its own inhibitor. Nature Structural & Molecular Biology
Juenemann K, Jansen AHP, van Riel L, et al. (2018) Dynamic recruitment of ubiquitin to mutant huntingtin inclusion bodies. Scientific Reports. 8: 1405
Ramirez YA, Adler TB, Altmann E, et al. (2018) Front Cover: Structural Basis of Substrate Recognition and Covalent Inhibition of Cdu1 from Chlamydia trachomatis (ChemMedChem 19/2018) Chemmedchem. 13: 2012-2012
Foote PK, Krist DT, Statsyuk AV. (2017) High-Throughput Screening of HECT E3 Ubiquitin Ligases Using UbFluor. Current Protocols in Chemical Biology. 9: 174-195
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