| Volkers, G.; Worrall, L.; Strynadka, N.C.J. (2015). Structure of human sialyltransferase ST8SiaIII in complex with CDP. Protein Data Bank: 5bo6. |
CMCF-BM |
PDB Deposition |
Health |
| Volkers, G.; Worrall, L.; Strynadka, N.C.J. (2015). Structure of human sialyltransferase ST8SiaIII in complex with CTP. Protein Data Bank: 5bo7. |
CMCF-BM |
PDB Deposition |
Health |
| Volkers, G.; Worrall, L.; Strynadka, N.C.J. (2015). Structure of human sialyltransferase ST8SiaIII. Protein Data Bank: 5bo8. |
CMCF-ID |
PDB Deposition |
Health |
| Von Kreudenstein, Thomas Spreter; Escobar-Carbrera, Eric; Lario, Paula I.; D’Angelo, Igor; Brault, Karine et al. (2013). Improving biophysical properties of a bispecific antibody scaffold to aid developability. mAbs 5(5) , 646-654. 10.4161/mabs.25632. [PDB: 4bsv, 4bsw] |
CMCF-BM |
Peer-Reviewed Article |
Health |
| Voth, K.; Chung, I.Y.W.; van Straaten, K.E.; Cygler, M. (2018). Structure of LpnE Effector Protein from Legionella pneumophila (sp. Philadelphia). Protein Data Bank: 6deh. |
CMCF-ID |
PDB Deposition |
Health |
| Voth, Kevin A.; Chung, Ivy Yeuk Wah; Straaten, Karin; Li, Lei; Boniecki, Michal T. et al. (2018). The structure of
Legionella
effector protein LpnE provides insights into its interaction with Oculocerebrorenal syndrome of Lowe (
OCRL
) protein. FEBS Journal 286(4) , 710-725. 10.1111/febs.14710. [PDB: 6deh] |
CMCF-ID |
Peer-Reviewed Article |
Health |
| Wagner, Florence F.; Benajiba, Lina; Campbell, Arthur J.; Weïwer, Michel; Sacher, Joshua R. et al. (2018). Exploiting an Asp-Glu “switch” in glycogen synthase kinase 3 to design paralog-selective inhibitors for use in acute myeloid leukemia. Science Translational Medicine 10(431) , eaam8460. 10.1126/scitranslmed.aam8460. [PDB: 5kpl, 5kpm] |
CMCF-ID |
Peer-Reviewed Article |
Health |
| Wahba, Haytham M.; Stevenson, Michael J.; Mansour, Ahmed; Sygusch, Jurgen; Wilcox, Dean E. et al. (2017). Structural and Biochemical Characterization of Organotin and Organolead Compounds Binding to the Organomercurial Lyase MerB Provide New Insights into Its Mechanism of Carbon–Metal Bond Cleavage. Journal of the American Chemical Society 139(2) , 910-921. 10.1021/jacs.6b11327. [PDB: 5u79, 5u7b, 5u7c, 5u82, 5u83] |
CMCF-ID |
Peer-Reviewed Article |
Health |
| Walker, J.R.; Qiu, L.; Butler-Cole, C.; Weigelt, J.; Bountra, C. et al. (2009). Crystal structure of the tandem IG-like C2-type 2 domains of the human mucosa-associated lymphoid tissue lymphoma translocation protein 1. Protein Data Bank: 3k0w. |
CMCF-ID |
PDB Deposition |
Health |
| Wang, H.; Tong, Y.; Nedyalkova, L.; Tempel, W.; Guan, X. et al. (2010). Crystal structure of ARFGAP1-ARF1 fusion protein. Protein Data Bank: 3o47. |
CMCF-ID |
PDB Deposition |
Health |
| Wang, W.; Bourhis, E.; Zhang, Y.; Rouge, L.; Wu, Y. et al. (2011). The structure of a beta propeller domain in complex with peptide S. Protein Data Bank: 3sov. |
CMCF-ID |
PDB Deposition |
Health |
| Wan, Honghe; Schroeder, Gretchen M.; Hart, Amy C.; Inghrim, Jennifer; Grebinski, James et al. (2015). Discovery of a Highly Selective JAK2 Inhibitor, BMS-911543, for the Treatment of Myeloproliferative Neoplasms. ACS Medicinal Chemistry Letters 6(8) , 850-855. 10.1021/acsmedchemlett.5b00226. [PDB: 5cf8] |
CMCF-ID |
Peer-Reviewed Article |
Health |
| Watanabe, Nobuhiko (2011). LL-Diaminopimelate Aminotransferase: The Mechanism of Substrate Recognition and Specificity. Supervisor: James, Michael N. G.. Alberta, Canada: University of Alberta. http://hdl.handle.net/10048/1649. |
CMCF-BM |
Doctoral Thesis |
Health |
| Watanabe, Nobuhiko; Clay, Matthew D.; van Belkum, Marco J.; Fan, Chenguang; Vederas, John C. et al. (2011). The Structure of ll-Diaminopimelate Aminotransferase from Chlamydia trachomatis: Implications for Its Broad Substrate Specificity. Journal of Molecular Biology 411(3) , 649-660. 10.1016/j.jmb.2011.06.023. [PDB: 3asb] |
CMCF-ID |
Peer-Reviewed Article |
Health |
| Watterson, Scott H.; De Lucca, George V.; Shi, Qing; Langevine, Charles M.; Liu, Qingjie et al. (2016). Discovery of 6-Fluoro-5-(R)-(3-(S)-(8-fluoro-1-methyl-2,4-dioxo-1,2-dihydroquinazolin-3(4H)-yl)-2-methylphenyl)-2-(S)-(2-hydroxypropan-2-yl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide (BMS-986142): A Reversible Inhibitor of Bruton’s Tyrosine Kinase (BTK) Conformationally Constrained by Two Locked Atropisomers. Journal of Medicinal Chemistry 59(19) , 9173-9200. 10.1021/acs.jmedchem.6b01088. [PDB: 5t18] |
CMCF-ID |
Peer-Reviewed Article |
Health |