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The Equine infectious anemia virus (EIAV) envelope glycoprotein gp45 is the transmembrane (TM) subunit of the viral envelope complex, produced by the proteolytic cleavage of the gp135 precursor protein [1]. It plays a critical role in the viral life cycle by mediating the fusion of the viral envelope with the host cell membrane, a process essential for the delivery of the viral genome into the cytoplasm [2]. Structurally, gp45 contains key functional domains including a hydrophobic fusion peptide, two heptad repeat regions (HR1 and HR2), and a transmembrane anchor [3]. During infection, gp45 undergoes a dramatic conformational change that brings the viral and cellular membranes into close proximity, facilitating pore formation [4]. Because of its central role in viral entry, gp45 is a primary target for the development of fusion inhibitors and subunit vaccines [5]. Experimental peptides derived from the HR2 region, such as EIAV-C45, have demonstrated the ability to block EIAV infection by interfering with the assembly of the six-helix bundle [6]. Understanding the dynamics of gp45 is vital for managing Equine Infectious Anemia, a persistent and potentially fatal disease in equids [7]. Sources: [1] UniProt P03322 (ENV_EIAV) [2] PubMed PMID: 11507211 [3] PubMed PMID: 15141005 [4] PubMed PMID: 12857894 [5] PubMed PMID: 21835158 [6] PubMed PMID: 15141005 [7] Merck Veterinary Manual - Equine Infectious Anemia
Inhibition of viral-host membrane fusion by binding to the heptad repeat regions of the transmembrane glycoprotein, preventing the formation of the six-helix bundle required for entry.
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