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  • PDB-101: Molecule of the Month: SARS-CoV-2 Spike
    Spike protein from SARS-CoV, with one receptor binding domain (RBD) in the up position, and a closed conformation of the SARS-CoV-2 spike The S1 fragment is shown in magenta and the S2 fragment in red, with glycosylation in lighter shades
  • Crystal structure of SARS-CoV-2 spike receptor-binding . . . - RCSB PDB
    Here, to better understand the initial step of infection at an atomic level, we determined the crystal structure of the receptor-binding domain (RBD) of the spike protein of SARS-CoV-2 bound to the cell receptor ACE2
  • 5DO2: Complex structure of MERS-RBD bound with 4C2 antibody - RCSB PDB
    Both mAbs potently bind to MERS-RBD and block virus entry in vitro with high efficacy We further investigated their mechanisms of neutralization by crystallizing the complex between the Fab fragments and the RBD, and solved the structure of the 4C2 Fab MERS-RBD complex
  • RCSB PDB - 6M17: The 2019-nCoV RBD ACE2-B0AT1 complex
    The 2019-nCoV RBD ACE2-B0AT1 complex Angiotensin-converting enzyme 2 (ACE2) is the cellular receptor for severe acute respiratory syndrome-coronavirus (SARS-CoV) and the new coronavirus (SARS-CoV-2) that is causing the serious coronavirus disease 2019 (COVID-19) epidemic Here, we present cryo-electron microscopy structures of full-length human ACE2 in the presence of the neutral amino acid
  • RCSB PDB - 8Z27: The structure of TGEV RBD and dog APN complex
    We further resolved the complex structures of dAPN bound to the PDCoV RBD TGEV RBD, respectively, establishing its divergent receptor-binding modes We identified R325 of dAPN as an important residue in the PDCoV RBD-dAPN interaction, and found the central role of Q746 and T749 in dAPN in the interaction with the TGEV RBD
  • RCSB PDB - 8Q93: Crystal structure of the SARS-COV-2 RBD with . . .
    Crystal structures of RBD-nanobody complexes reveal how ACE2-binding is blocked and also explain the nanobodies' tolerance to immune escape mutations Through the cryo-EM structure of the Ma16B06-BA 1 Spike complex, we demonstrated how a single nanobody molecule can neutralize a trimeric spike
  • RCSB PDB - 9IU1: Structure of SARS-CoV-2 JN. 1 spike RBD in complex with . . .
    The SARS-CoV-2 spike protein, crucial for cellular entry, binds to the ACE2 receptor exclusively when its receptor-binding domain (RBD) adopts the up-conformation However, whether ACE2 also interacts with the RBD in the down-conformation to facilitate the conformational shift to RBD-up remains unclear
  • RCSB PDB - 8YZD: Structure of JN. 1 RBD protein in complex with ACE2.
    Structure of JN 1 RBD protein in complex with ACE2
  • RCSB PDB - 7R6X: SARS-CoV-2 spike receptor-binding domain (RBD) in . . .
    Here we comprehensively characterize escape, breadth and potency across a panel of SARS-CoV-2 antibodies targeting the receptor-binding domain (RBD) Despite a trade-off between in vitro neutralization potency and breadth of sarbecovirus binding, we identify neutralizing antibodies with exceptional sarbecovirus breadth and a corresponding





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