Biophysics
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Transformations, Lineage Comparisons, and Analysis of Down to Up Protomer States of Variants of the SARS-CoV-2 Prefusion Spike Protein Including the UK Variant B.1.1.7
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Allosteric Cross-Talk Among SARS-CoV-2 Spike’s Receptor-Binding Domain Mutations Triggers an Effective Hijacking of Human Cell Receptor
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Fine-tuning the Spike: Role of the nature and topology of the glycan shield in the structure and dynamics of the SARS-CoV-2 S
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Modelling conformational state dynamics and its role on infection for SARS-CoV-2 Spike protein variants
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A glycan gate controls opening of the SARS-CoV-2 spike protein
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Inferring the stabilization effects of SARS-CoV-2 variants on the binding with ACE2 receptor
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Molecular dynamic simulation reveals E484K mutation enhances spike RBD-ACE2 affinity and the combination of E484K, K417N and N501Y mutations (501Y.V2 variant) induces conformational change greater than N501Y mutant alone, potentially resulting in an escape mutant
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Structural basis of anti-SARS-CoV-2 activity of HCQ: specific binding to N protein to disrupt its interaction with nucleic acids and LLPS
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N-Terminal finger stabilizes the reversible feline drug GC376 in SARS-CoV-2 M pro
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The nucleotide addition cycle of the SARS-CoV-2 polymerase
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