S. Shenoy

发表

Griffithsin tandemers: flexible and potent lectin inhibitors of the human immunodeficiency virus

S. Subramaniam, A. Wlodawer, J. Meyerson, 2015, Retrovirology.

Analysis of the interaction between the HIV-inactivating protein cyanovirin-N and soluble forms of the envelope glycoproteins gp120 and gp41.

M. Boyd, D. Xie, I. Chaiken, 2000, Molecular pharmacology.

Biophysical studies of DNA modified with conformationally constrained nucleotides: comparison of 2′-exo (north) and 3′-exo (south) ‘locked’ templates

V. Marquez, Que N. Van, J. Barchi, 2007, Nucleic acids research.

The Natural Product Butylcycloheptyl Prodiginine Binds Pre-miR-21, Inhibits Dicer-Mediated Processing of Pre-miR-21, and Blocks Cellular Proliferation.

S. Lockett, Cheryl L. Thomas, E. Goncharova, 2019, Cell chemical biology.

Broad-Spectrum In Vitro Activity and In Vivo Efficacy of the Antiviral Protein Griffithsin against Emerging Viruses of the Family Coronaviridae

D. Meyerholz, J. Mcmahon, C. Wohlford-Lenane, 2009, Journal of Virology.

Structures of the Complexes of a Potent Anti-HIV Protein Cyanovirin-N and High Mannose Oligosaccharides*

Alexander Wlodawer, Peter H Seeberger, Barry R O'Keefe, 2002, The Journal of Biological Chemistry.

Structural and functional analyses of minimal phosphopeptides targeting the polo-box domain of polo-like kinase 1

Fa Liu, Marc C. Nicklaus, Dong-Hee Lee, 2009, Nature Structural &Molecular Biology.

Monomerization of Viral Entry Inhibitor Griffithsin Elucidates the Relationship between Multivalent Binding to Carbohydrates and anti-HIV Activity

A. Wlodawer, Z. Dauter, Cheryl L. Thomas, 2010, Structure.

Multisite and multivalent binding between cyanovirin-N and branched oligomannosides: calorimetric and NMR characterization.

A. Gronenborn, M. Boyd, P. Seeberger, 2002, Chemistry & biology.

Cyanovirin-N defines a new class of antiviral agent targeting N-linked, high-mannose glycans in an oligosaccharide-specific manner.

M. Boyd, J. Mcmahon, B. O’Keefe, 2001, Molecular pharmacology.

Selective interactions of the human immunodeficiency virus-inactivating protein cyanovirin-N with high-mannose oligosaccharides on gp120 and other glycoproteins.

M. Boyd, B. O’Keefe, S. Shenoy, 2001, The Journal of pharmacology and experimental therapeutics.

Physicochemical characterization of the recombinant lectin scytovirin and microbicidal activity of the SD1 domain produced in rice against HIV-1

S. Marfil, P. Christou, T. Capell, 2022, Plant Cell Reports.

Crystallographic, thermodynamic, and molecular modeling studies of the mode of binding of oligosaccharides to the potent antiviral protein griffithsin† ‡

R. Dwek, A. Wlodawer, M. Wormald, 2007, Proteins.

Broad-Spectrum In Vitro Activity and In Vivo Efficacy of the Antiviral Protein Griffithsin against Emerging Viruses of the Family Coronaviridae

D. Meyerholz, J. Mcmahon, C. Wohlford-Lenane, 2010, Journal of Virology.

Identification of Biologically Active, HIV TAR RNA-Binding Small Molecules Using Small Molecule Microarrays

S. L. Le Grice, Joanna Sztuba-Solinska, Peter C. Gareiss, 2014, Journal of the American Chemical Society.

Structural and functional analyses of minimal phosphopeptides targeting the polo-box domain of polo-like kinase 1

Fa Liu, Dong-Hee Lee, Jung-Eun Park, 2009, Nature Structural &Molecular Biology.

Preclinical Manufacture of Anti‐HER2 Liposome‐Inserting, scFv‐PEG‐Lipid Conjugate. 2. Conjugate Micelle Identity, Purity, Stability, and Potency Analysis

John W. Park, J. Marks, D. Drummond, 2008, Biotechnology progress.

Functional analysis of the fission yeast Prp4 protein kinase involved in pre-mRNA splicing and isolation of a putative mammalian homologue.

A. Klingenhoff, S. Shenoy, M. Lützelberger, 1997, Nucleic acids research.

Complex interactions of HIV-1 nucleocapsid protein with oligonucleotides

Robert H. Shoemaker, Daniele Fabris, Andrew G. Stephen, 2006, Nucleic Acids Research.

Discovery and Characterization of a Biologically Active Non–ATP-Competitive p38 MAP Kinase Inhibitor

Jason R. Evans, P. Wipf, E. Goncharova, 2016, Journal of biomolecular screening.

Crystallographic studies of the complexes of antiviral protein griffithsin with glucose and N-acetylglucosamine

A. Wlodawer, B. O’Keefe, N. E. Ziółkowska, 2007, Protein science : a publication of the Protein Society.

ENGINEERING DNA TOPOLOGY WITH LOCKED NUCLEOSIDES: A STRUCTURAL STUDY

A. Bax, Justin Wu, V. Marquez, 2005, Nucleosides, nucleotides & nucleic acids.

Cyanovirin-N binds to select SARS-CoV-2 spike oligosaccharides outside of the receptor binding domain and blocks infection by SARS-CoV-2

S. Marfil, R. Twyman, A. Tanuri, 2023, Proceedings of the National Academy of Sciences of the United States of America.

KDM3B inhibitors disrupt the oncogenic activity of PAX3-FOXO1 in fusion-positive rhabdomyosarcoma

B. Gryder, Xinyu Wen, Benjamin Z. Stanton, 2024, Nature communications.

Structural and functional analyses of minimal phosphopeptides targeting the polo-box domain of polo-like kinase 1

M. Yaffe, A. Wlodawer, E. Appella, 2011, Nature Structural &Molecular Biology.