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Proceedings of the National Academy of Sciences of the United States of America|May 31, 2008
ALIX-CHMP4 interactions in the human ESCRT pathwayJohn McCullough, Robert D Fisher, Frank G Whitby, et al.Nature Communications|June 9, 2026
Structural basis of insulin receptor antagonism by bivalent site 1-site 2 ligands S961 and Ins-AC-S2Amber Vogel, Alan Blakely, Yuankun Dao, et al.Journal of Molecular Biology|February 19, 2008
Cryo-EM structure of dodecameric Vps4p and its 2:1 complex with Vta1pZhiheng Yu, Malgorzata D Gonciarz, Wesley I Sundquist, et al.Journal of Molecular Biology|June 25, 2002
Crystal structure of a biliverdin IXalpha reductase enzyme-cofactor complexFrank G Whitby, John D Phillips, Christopher P Hill, et al.Molecular Cell|October 13, 2015
FACT Disrupts Nucleosome Structure by Binding H2A-H2B with Conserved Peptide MotifsDavid J Kemble, Laura L McCullough, Frank G Whitby, et al.The Journal of Biological Chemistry|April 3, 2015
Binding of Substrates to the Central Pore of the Vps4 ATPase Is Autoinhibited by the Microtubule Interacting and Trafficking (MIT) Domain and Activated by MIT Interacting Motifs (MIMs)Han Han, Nicole Monroe, Jörg Votteler, et al.Molecular Cell|May 9, 2006
The structure of the yFACT Pob3-M domain, its interaction with the DNA replication factor RPA, and a potential role in nucleosome depositionAndrew P VanDemark, Mary Blanksma, Elliott Ferris, et al.Biorxiv : the Preprint Server for Biology|September 2, 2025
Structural basis of insulin receptor antagonism by bivalent site 1-site 2 ligandsAmber Vogel, Alan Blakely, Yuankun Dao, et al.Proceedings of the National Academy of Sciences of the United States of America|October 19, 2007
Potent D-peptide inhibitors of HIV-1 entryBrett D Welch, Andrew P VanDemark, Annie Heroux, et al.Journal of Molecular Biology|April 14, 2009
Substrate shuttling between active sites of uroporphyrinogen decarboxylase is not required to generate coproporphyrinogenJohn D Phillips, Christy A Warby, Frank G Whitby, et al.Pageof 15