Perspectives on Molecular Mimicry Between Human, SARS-CoV-2, and Plasmodium Species Through a Probabilistic and Evolutionary Insight

Yekbun Adiguzel, Yehuda Shoenfeld

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Abstract

This chapter examines potential molecular mimicry between similar peptide sequences and shared 6mers of five selected proteins and the proteomes of both SARS-CoV-2 and five Plasmodium species that infect humans (P. falciparum, P. malariae, P. vivax, P. knowlesi, and P. ovale). Human proteins are plasminogen receptor (KT), neutrophil collagenase (neutrophil collagenase isoform 2), myeloperoxidase precursor, mitochondrial peptide methionine sulfoxide reductase isoform a precursor, and myeloblastin precursor. The chapter eventually focuses on a probabilistic and evolutionary insight into molecular mimicry.

Original languageEnglish
Title of host publicationInfection and Autoimmunity
PublisherElsevier
Pages27-42
Number of pages16
ISBN (Electronic)9780323991308
ISBN (Print)9780323991315
DOIs
StatePublished - 1 Jan 2024

Keywords

  • Amino acid fraction
  • Autoimmune disease
  • COVID-19
  • HLA affinity
  • MHC
  • Peptide similarity

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