Sergey G. Tarasov

Bisimidazoacridones: 2. Steady-state and time-resolved fluorescence studies of their diverse interactions with DNA.

Transmembrane inhibitors of P-glycoprotein, an ABC transporter.

Structural analogues of smoothened intracellular loops as potent inhibitors of Hedgehog pathway and cancer cell growth.

Rationally designed inhibitors identify STAT3 N-domain as a promising anticancer drug target.

Structural basis for high-affinity peptide inhibition of p53 interactions with MDM2 and MDMX.

Engineered human antibody constant domains with increased stability.

Allosteric activation of E2-RING finger-mediated ubiquitylation by a structurally defined specific E2-binding region of gp78.

Limitations of peptide retro-inverso isomerization in molecular mimicry.

Peptide structure stabilization by membrane anchoring and its general applicability to the development of potent cell-permeable inhibitors.

Structural plasticity of a transmembrane peptide allows self-assembly into biologically active nanoparticles.

The Era GTPase recognizes the GAUCACCUCC sequence and binds helix 45 near the 3' end of 16S rRNA.

Structural basis for RNA recognition by NusB and NusE in the initiation of transcription antitermination.

Mechanisms of unphosphorylated STAT3 transcription factor binding to DNA.

β-Defensin 2 and 3 Promote the Uptake of Self or CpG DNA, Enhance IFN-α Production by Human Plasmacytoid Dendritic Cells, and Promote Inflammation.

Allosteric regulation of E2:E3 interactions promote a processive ubiquitination machine.