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Viral hijacking mechanism in humans through protein-protein interactions.
Selvaraj, Chandrabose; Shri, Gurunathan Rubha; Vijayakumar, Rajendran; Alothaim, Abdulaziz S; Ramya, Saravanan; Singh, Sanjeev Kumar.
  • Selvaraj C; Computer Aided Drug Design and Molecular Modeling Lab, Department of Bioinformatics, Science Block, Alagappa University, Karaikudi, Tamil Nadu, India. Electronic address: drbioselva@gmail.com.
  • Shri GR; Computer Aided Drug Design and Molecular Modeling Lab, Department of Bioinformatics, Science Block, Alagappa University, Karaikudi, Tamil Nadu, India.
  • Vijayakumar R; Department of Biology, College of Science in Zulfi, Majmaah University, Majmaah, Saudi Arabia.
  • Alothaim AS; Department of Biology, College of Science in Zulfi, Majmaah University, Majmaah, Saudi Arabia.
  • Ramya S; Computer Aided Drug Design and Molecular Modeling Lab, Department of Bioinformatics, Science Block, Alagappa University, Karaikudi, Tamil Nadu, India.
  • Singh SK; Computer Aided Drug Design and Molecular Modeling Lab, Department of Bioinformatics, Science Block, Alagappa University, Karaikudi, Tamil Nadu, India. Electronic address: skysanjeev@gmail.com.
Adv Protein Chem Struct Biol ; 131: 261-276, 2022.
Article in English | MEDLINE | ID: covidwho-1866754
ABSTRACT
Numerous viruses have evolved mechanisms to inhibit or alter the host cell's apoptotic response as part of their coevolution with their hosts. The analysis of virus-host protein interactions require an in-depth understanding of both the viral and host protein structures and repertoires, as well as evolutionary mechanisms and pertinent biological facts. Throughout the course of a viral infection, there is constant battle for binding between virus and cellular proteins. Exogenous interfaces facilitating viral-host interactions are well known for constantly targeting and suppressing endogenous interfaces mediating intraspecific interactions, such as viral-viral and host-host connections. In these interactions, the protein-protein interactions (PPIs), are mostly shown as networks (protein interaction networks, PINs), with proteins represented as nodes and their interactions represented as edges. Host proteins with a higher degree of connectivity are more likely to interact with viral proteins. Due to technical advancements, three-dimensional interactions may now be visualized computationally utilizing molecular modeling and cryo-EM approaches. The uniqueness of viral domain repertoires, their evolution, and their activities during viral infection make viruses fascinating models for research. This chapter aims to provide readers a complete picture of the viral hijacking mechanism in protein-protein interactions.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Proteins / Host Microbial Interactions Type of study: Prognostic study Limits: Humans Language: English Journal: Adv Protein Chem Struct Biol Journal subject: Biology / Biochemistry Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Proteins / Host Microbial Interactions Type of study: Prognostic study Limits: Humans Language: English Journal: Adv Protein Chem Struct Biol Journal subject: Biology / Biochemistry Year: 2022 Document Type: Article