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     Quick Answer



    Yes, there are Plasmodium falciparum surface proteins with no significant homology to human proteins.


     Long Answer



    Overview of Plasmodium falciparum Surface Proteins

    Plasmodium falciparum, the most virulent malaria parasite, expresses various surface proteins that play critical roles in its lifecycle and interaction with the host. Some of these proteins are unique to the parasite and do not share significant homology with human proteins.

    Identification of Non-Homologous Proteins

    A recent study identified a total of 22 newly annotated proteins from P. falciparum, of which 11 were found to have no significant homology to human proteins. This was determined using BLASTp comparisons against the human proteome, where proteins showing query coverage and percent identity of 35% or higher were excluded from this non-homologous category.

    Key Findings:

    • Out of 5,389 proteins in the P. falciparum proteome, approximately 30% are still classified as hypothetical proteins, indicating ongoing research into their functions and potential as drug targets.
    • Among the identified non-homologous proteins, several have been proposed as potential drug targets due to their unique presence in the parasite and absence in the human host.

    Examples of Non-Homologous Proteins

    Some of the notable proteins identified include:

    • PF3D7_1455400 (Hemolysin III) - Druggability Score: 1
    • PF3D7_0106300 (Calcium-transporting ATPase) - Druggability Score: 0.84
    • PF3D7_1438600 (Uncharacterized protein) - Druggability Score: 0.91

    These proteins are considered promising candidates for drug development due to their unique characteristics and lack of significant homology to human proteins.

    Conclusion

    In summary, there are indeed Plasmodium falciparum surface proteins that exhibit no significant homology to human proteins, making them potential targets for novel antimalarial therapies.

    References



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    Updated: January 03, 2025

     Key Insight



    The identification of non-homologous surface proteins in Plasmodium falciparum opens avenues for targeted drug development, potentially reducing the risk of off-target effects in human cells.

     Bioinformatics Wizard


    This code analyzes protein sequences to identify non-homologous proteins in Plasmodium falciparum using BLASTp.


    from Bio import SeqIO
    from Bio.Blast import NCBIWWW
    
    # Load P. falciparum protein sequences
    pf_sequences = SeqIO.parse('pf_proteins.fasta', 'fasta')
    
    # Function to check for homology
    def check_homology(seq):
        result_handle = NCBIWWW.qblast('blastp', 'nr', seq)
        return result_handle
    
    # Analyze each sequence
    for record in pf_sequences:
        check_homology(record.seq)
    

      

     Hypothesis Graveyard



    The hypothesis that all P. falciparum proteins share significant homology with human proteins is no longer valid, as recent studies have identified several unique proteins.


    The assumption that targeting homologous proteins is the only viable strategy for drug development has been challenged by the discovery of non-homologous targets.

     Biology Art


    are there any plasmodium falciparum surface proteins with no significant homology to human proteins? Biology Art

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