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10.1007/s10930-020-09933-w

http://scihub22266oqcxt.onion/10.1007/s10930-020-09933-w
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33098476!7584483!33098476
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suck abstract from ncbi


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pmid33098476      Protein+J 2020 ; 39 (6): 600-618
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  • An Overview of the Crystallized Structures of the SARS-CoV-2 #MMPMID33098476
  • Ionescu MI
  • Protein J 2020[Dec]; 39 (6): 600-618 PMID33098476show ga
  • Many research teams all over the world focus their research on the SARS-CoV-2, the new coronavirus that causes the so-called COVID-19 disease. Most of the studies identify the main protease or 3C-like protease (M(pro)/3CL(pro)) as a valid target for large-spectrum inhibitors. Also, the interaction of the human receptor angiotensin-converting enzyme 2 (ACE2) with the viral surface glycoprotein (S) is studied in depth. Structural studies tried to identify the residues responsible for enhancement/weaken virus-ACE2 interactions or the cross-reactivity of the neutralizing antibodies. Although the understanding of the immune system and the hyper-inflammatory process in COVID-19 are crucial for managing the immediate and the long-term consequences of the disease, not many X-ray/NMR/cryo-EM crystals are available. In addition to 3CL(pro), the crystal structures of other nonstructural proteins offer valuable information for elucidating some aspects of the SARS-CoV-2 infection. Thus, the structural analysis of the SARS-CoV-2 is currently mainly focused on three directions-finding M(pro)/3CL(pro) inhibitors, the virus-host cell invasion, and the virus-neutralizing antibody interaction.
  • |Amino Acid Sequence[MESH]
  • |Antiviral Agents/pharmacology[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |COVID-19/*virology[MESH]
  • |Coronavirus 3C Proteases/antagonists & inhibitors/*chemistry[MESH]
  • |Coronavirus Nucleocapsid Proteins/antagonists & inhibitors/*chemistry[MESH]
  • |Coronavirus Papain-Like Proteases/antagonists & inhibitors/*chemistry[MESH]
  • |Coronavirus RNA-Dependent RNA Polymerase/antagonists & inhibitors/*chemistry[MESH]
  • |Cryoelectron Microscopy[MESH]
  • |Crystallography, X-Ray[MESH]
  • |Drug Discovery[MESH]
  • |Humans[MESH]
  • |Models, Molecular[MESH]
  • |Nuclear Magnetic Resonance, Biomolecular[MESH]
  • |Phosphoproteins/antagonists & inhibitors/chemistry[MESH]
  • |Protein Conformation[MESH]
  • |Protein Kinase Inhibitors/pharmacology[MESH]


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