Structural basis of influenza virus fusion inhibition by the antiviral drug Arbidol von Kadam, Rameshwar U., Wilson, Ian A.

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Design of protein-binding proteins from the target structure alone von Cao, Longxing, Coventry, Brian, Goreshnik, Inna, Huang, Buwei, Sheffler, William, Park, Joon Sung, Jude, Kevin M., Marković, Iva, Kadam, Rameshwar U., Verschueren, Koen H. G., Verstraete, Kenneth, Walsh, Scott Thomas Russell, Bennett, Nathaniel, Phal, Ashish, Yang, Aerin, Kozodoy, Lisa, DeWitt, Michelle, Picton, Lora, Miller, Lauren, Strauch, Eva-Maria, DeBouver, Nicholas D., Pires, Allison, Bera, Asim K., Halabiya, Samer, Hammerson, Bradley, Yang, Wei, Bernard, Steffen, Stewart, Lance, Wilson, Ian A., Ruohola-Baker, Hannele, Schlessinger, Joseph, Lee, Sangwon, Savvides, Savvas N., Garcia, K. Christopher, Baker, David

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Hepatitis C Virus E2 Envelope Glycoprotein Core Structure von Kong, Leopold, Giang, Erick, Nieusma, Travis, Kadam, Rameshwar U., Cogburn, Kristin E., Hua, Yuanzi, Dai, Xiaoping, Stanfield, Robyn L., Burton, Dennis R., Ward, Andrew B., Wilson, Ian A., Law, Mansun

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Potent peptidic fusion inhibitors of influenza virus von Kadam, Rameshwar U., Juraszek, Jarek, Brandenburg, Boerries, Buyck, Christophe, Schepens, Wim B. G., Kesteleyn, Bart, Stoops, Bart, Vreeken, Rob J., Vermond, Jan, Goutier, Wouter, Tang, Chan, Vogels, Ronald, Friesen, Robert H. E., Goudsmit, Jaap, van Dongen, Maria J. P., Wilson, Ian A.

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Structural flexibility at a major conserved antibody target on hepatitis C virus E2 antigen von Kong, Leopold, Lee, David E., Kadam, Rameshwar U., Liu, Tong, Giang, Erick, Nieusma, Travis, Garces, Fernando, Tzarum, Netanel, Woods, Virgil L., Ward, Andrew B., Li, Sheng, Wilson, Ian A., Law, Mansun

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Preventing an Antigenically Disruptive Mutation in Egg-Based H3N2 Seasonal Influenza Vaccines by Mutational Incompatibility von Wu, Nicholas C., Lv, Huibin, Thompson, Andrew J., Wu, Douglas C., Ng, Wilson W.S., Kadam, Rameshwar U., Lin, Chih-Wei, Nycholat, Corwin M., McBride, Ryan, Liang, Weiwen, Paulson, James C., Mok, Chris K.P., Wilson, Ian A.

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A small-molecule fragment that emulates binding of receptor and broadly neutralizing antibodies to influenza A hemagglutinin von Kadam, Rameshwar U., Wilson, Ian A.

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Structure and Function of a Novel ld-Carboxypeptidase A Involved in Peptidoglycan Recycling von Das, Debanu, Hervé, Mireille, Elsliger, Marc-André, Kadam, Rameshwar U, Grant, Joanna C, Chiu, Hsiu-Ju, Knuth, Mark W, Klock, Heath E, Miller, Mitchell D, Godzik, Adam, Lesley, Scott A, Deacon, Ashley M, Mengin-Lecreulx, Dominique, Wilson, Ian A

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Glycopeptide Dendrimers with High Affinity for the Fucose‐Binding Lectin LecB from Pseudomonas aeruginosa von Kolomiets, Elena, Swiderska, Magdalena A., Kadam, Rameshwar U., Johansson, Emma M. V., Jaeger, Karl‐Erich, Darbre, Tamis, Reymond, Jean‐Louis

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Structure-based optimization and synthesis of antiviral drug Arbidol analogues with significantly improved affinity to influenza hemagglutinin von Wright, Zoë V.F., Wu, Nicholas C., Kadam, Rameshwar U., Wilson, Ian A., Wolan, Dennis W.

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An influenza A hemagglutinin small-molecule fusion inhibitor identified by a new high-throughput fluorescence polarization screen von Yao, Yao, Kadam, Rameshwar U., Lee, Chang-Chun David, Woehl, Jordan L., Wu, Nicholas C., Zhu, Xueyong, Kitamura, Seiya, Wilson, Ian A., Wolan, Dennis W.

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Ultrapotent influenza hemagglutinin fusion inhibitors developed through SuFEx-enabled high-throughput medicinal chemistry von Kitamura, Seiya, Lin, Ting-Hui, Lee, Chang-Chun David, Takamura, Akihiro, Kadam, Rameshwar U, Zhang, Ding, Zhu, Xueyong, Dada, Lucas, Nagai, Emiko, Yu, Wenli, Yao, Yao, Sharpless, K Barry, Wilson, Ian A, Wolan, Dennis W

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CH−π “T-Shape” Interaction with Histidine Explains Binding of Aromatic Galactosides to Pseudomonas aeruginosa Lectin LecA von Kadam, Rameshwar U, Garg, Divita, Schwartz, Julian, Visini, Ricardo, Sattler, Michael, Stocker, Achim, Darbre, Tamis, Reymond, Jean-Louis

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A Glycopeptide Dendrimer Inhibitor of the Galactose-Specific Lectin LecA and of Pseudomonas aeruginosa Biofilms von Kadam, Rameshwar U., Bergmann, Myriam, Hurley, Matthew, Garg, Divita, Cacciarini, Martina, Swiderska, Magdalena A., Nativi, Cristina, Sattler, Michael, Smyth, Alan R., Williams, Paul, Cámara, Miguel, Stocker, Achim, Darbre, Tamis, Reymond, Jean-Louis

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Structure-Based Optimization of the Terminal Tripeptide in Glycopeptide Dendrimer Inhibitors of Pseudomonas aeruginosa Biofilms Targeting LecA von Kadam, Rameshwar U., Bergmann, Myriam, Garg, Divita, Gabrieli, Gabriele, Stocker, Achim, Darbre, Tamis, Reymond, Jean-Louis

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Structure of Hepatitis C Virus Envelope Glycoprotein E1 Antigenic Site 314–324 in Complex with Antibody IGH526 von Kong, Leopold, Kadam, Rameshwar U., Giang, Erick, Ruwona, Tinashe B., Nieusma, Travis, Culhane, Jeffrey C., Stanfield, Robyn L., Dawson, Philip E., Wilson, Ian A., Law, Mansun

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An alternate conformation of HCV E2 neutralizing face as an additional vaccine target von Tzarum, Netanel, Giang, Erick, Kadam, Rameshwar U., Chen, Fang, Nagy, Kenna, Augestad, Elias H., Velazquez-Moctezuma, Rodrigo, Keck, Zhen-Yong, Hua, Yuanzi, Stanfield, Robyn L., Dreux, Marlene, Prentoe, Jannick, Foung, Steven K. H., Bukh, Jens, Wilson, Ian A., Law, Mansun

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Expanding the accessible chemical space by solid phase synthesis of bicyclic homodetic peptides von Bartoloni, Marco, Kadam, Rameshwar U, Schwartz, Julian, Furrer, Julien, Darbre, Tamis, Reymond, Jean-Louis

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Membrane disrupting antimicrobial peptide dendrimers with multiple amino termini von Stach, Michaela, Maillard, Noélie, Kadam, Rameshwar U., Kalbermatter, David, Meury, Marcel, Page, Malcolm G. P., Fotiadis, Dimitrios, Darbre, Tamis, Reymond, Jean-Louis

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Cluster analysis and two-dimensional quantitative structure–activity relationship (2D-QSAR) of Pseudomonas aeruginosa deacetylase LpxC inhibitors von Kadam, Rameshwar U., Roy, Nilanjan

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