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Plos One|May 27, 2016
Crystal Structure of the FERM-SH2 Module of Human Jak2Randall McNally, Angela V Toms, Michael J EckActa Crystallographica. Section D, Biological Crystallography|October 22, 2005
Novel multisubstrate inhibitors of mammalian purine nucleoside phosphorylaseAngela V Toms, Weiru Wang, Yingbo Li, et al.The Journal of Biological Chemistry|May 20, 2004
Evolutionary links as revealed by the structure of Thermotoga maritima S-adenosylmethionine decarboxylaseAngela V Toms, Cynthia Kinsland, Diane E McCloskey, et al.ACS Chemical Biology|September 1, 2010
Binucleine 2, an isoform-specific inhibitor of Drosophila Aurora B kinase, provides insights into the mechanism of cytokinesisYegor Smurnyy, Angela V Toms, Gilles R Hickson, et al.Biochemistry|February 16, 2005
Structural characterization of the regulatory proteins TenA and TenI from Bacillus subtilis and identification of TenA as a thiaminase IIAngela V Toms, Amy L Haas, Joo-Heon Park, et al.Molecular Cell|March 31, 2019
Distinct USP25 and USP28 Oligomerization States Regulate Deubiquitinating ActivityMalte Gersch, Jane L Wagstaff, Angela V Toms, et al.Proceedings of the National Academy of Sciences of the United States of America|July 7, 2011
Structure and function of the interacting domains of Spire and Fmn-family forminsChristina L Vizcarra, Barry Kreutz, Avital A Rodal, et al.Proceedings of the National Academy of Sciences of the United States of America|January 30, 2008
The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATPCai-Hong Yun, Kristen E Mengwasser, Angela V Toms, et al.Plos One|March 30, 2011
Crystal structure of a coiled-coil domain from human ROCK IDaqi Tu, Yiqun Li, Hyun Kyu Song, et al.Nature Structural & Molecular Biology|September 10, 2013
Structure of a pseudokinase-domain switch that controls oncogenic activation of Jak kinasesAngela V Toms, Anagha Deshpande, Randall McNally, et al.Pageof 2