Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/59771
Title: Structure-function relationships among selected human coronaviruses
Authors: Jamir, Esther
Kiewhuo, Kikrusenuo
Priyadarsinee, Lipsa
Sarma, Himakshi
Nagamani, Selvaraman
Sastry, G Narahari
Keywords: Hotspot residues;Multiple sequence alignment;Protein-protein interaction;Seven human coronaviruses
Issue Date: May-2022
Publisher: NIScPR-CSIR, India
Abstract: Identifying the key proteins among different types of human disease-causing coronaviruses is essential for the molecular mechanism and thereby designing potential drug molecules. Eight selected proteins of seven types of disease-causing coronaviruses, viz.SARS-CoV-2 (severe acute respiratory syndrome coronavirus2), SARS-CoV (severe acute respiratory syndrome coronavirus), MERS-CoV (middle east respiratory syndrome coronavirus), Human coronavirus OC43, Human coronavirus HKU1, Human coronavirus 229E and Human coronavirus NL63, were chosen for the comparison. Further, an attempt has been made to explore the most important host-pathogen interactions with a special focus on spike (RBD) protein region as this region deemed to be functionally most important. Epitope region was also identified which helps in the design of epitope-based vaccines. The structural comparison carried out among the seven types of human coronaviruses has revealed the molecular level details on the similarity among this series. This study has facilitated the identification of the important residues in the studied proteins which control the key functions such as viral replication and transmission. Thus, exploring the protein space in the family of coronaviruses, provide valuable insights into the molecular basis associated with the role of proteins and viral infections, which is expected to trigger the identification of the drug targets for coronaviruses infections, in a rational way.
Page(s): 536-551
ISSN: 0975-0959 (Online); 0301-1208 (Print)
Appears in Collections:IJBB Vol.59(05) [May 2022]

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IJBB 59(5) 536-551 Suppl.pdfSupplementary Data6.99 MBAdobe PDFView/Open
IJBB 59(5) 536-551 Suppl. Tables.pdfSupplementary Tables175.83 kBAdobe PDFView/Open


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