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  • RCSB PDB - 9ML8: Crystal structure of the SARS-CoV-2 RBD in complex . . .
    Broad immune responses are needed to mitigate viral evolution and escape To induce antibodies against conserved receptor-binding domain (RBD) regions of SARS-like betacoronavirus (sarbecovirus) spike proteins that recognize SARS-CoV-2 variants of concern and zoonotic sarbecoviruses, we developed mosaic-8b RBD nanoparticles presenting eight sarbecovirus RBDs arranged randomly on a 60-mer
  • RCSB PDB - 9ELJ: Cryo-EM structure of SARS-CoV-2 Omicron JN. 1. 11+Q493E . . .
    Cryo-EM structure of SARS-CoV-2 Omicron JN 1 11+Q493E+S31deletion spike protein (one RBD up state)
  • RCSB PDB - 9ELH: Cryo-EM structure of SARS-CoV-2 Omicron KP. 3. 1. 1 spike . . .
    Cryo-EM structure of SARS-CoV-2 Omicron KP 3 1 1 spike protein (one RBD up state)
  • Crystal structure of SARS-CoV-2 spike receptor-binding . . . - RCSB PDB
    A new and highly pathogenic coronavirus (severe acute respiratory syndrome coronavirus-2, SARS-CoV-2) caused an outbreak in Wuhan city, Hubei province, China, starting from December 2019 that quickly spread nationwide and to other countries around the world 1-3 Here, to better understand the initial step of infection at an atomic level, we determined the crystal structure of the receptor
  • Molecule of the Month: SARS-CoV-2 Spike - RCSB: PDB-101
    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
  • RCSB PDB - 7L4Z: Structure of SARS-CoV-2 spike RBD in complex with . . .
    The COVID-19 pandemic, caused by SARS-CoV-2, has led to substantial morbidity, mortality, and disruption globally Cellular entry of SARS-CoV-2 is mediated by the viral spike protein, and affinity ligands to this surface protein have the potential for applications as antivirals and diagnostic reagents
  • RCSB PDB - 9IU1: Structure of SARS-CoV-2 JN. 1 spike RBD in complex with . . .
    Since 2019, SARS-CoV-2 has undergone mutations, resulting in pandemic and epidemic waves 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
  • RCSB PDB - 6M1D: ACE2-B0AT1 complex, open conformation
    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
  • 7BWJ: crystal structure of SARS-CoV-2 antibody with RBD - RCSB PDB
    The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) presents a global health emergency that is in urgent need of intervention 1-3 The entry of SARS-CoV-2 into its target cells depends on binding between the receptor-binding domain (RBD) of the viral spike protein and its cellular receptor, angiotensin-converting enzyme 2
  • 7Y72 - RCSB PDB
    The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern such as Omicron hampered efforts in controlling the ongoing coronavirus disease 2019 pandemic due to their ability to escape neutralizing antibodies induced by vaccination or prior infection, highlighting the need to develop broad-spectrum vaccines and therapeutics





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