β Pore-forming Protein-based Evolutionary Divergence of Gnathostomata from Agnatha

Author:

Kumar Bhupendra1,Kashif Mohd2,Alsaiari Ahad Amer3,Khan Mohammad Imran4,Kalam Abul5,Ahmad Abrar4,Lone Rayees Ahmad1,Almehmadi Mazen3,Dudhagi Shivanand Suresh1,Zamzami Mazin A4

Affiliation:

1. Center for Plant Molecular Biology and Biotechnology Division, CSIR-National Botanical Research Institute, Rana Pratap Marg, Lucknow-226001, U.P., India

2. Department of Biotechnology, Babasaheb Bhimrao Ambedkar University, Lucknow, India

3. Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia

4. Department of Biochemistry, King Abdulaziz University, Jeddah, Saudi Arabia

5. Department of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, India

Abstract

Introduction: The first vertebrates were jawless fish, or Agnatha, whose evolution diverged into jawed fish, or Gnathostomes, around 550 million years ago. Methods: In this study, we investigated β PFT proteins' evolutionary divergence of lamprey immune protein from Agnatha, reportedly possessing anti-cancer activity, into Dln1 protein from Gnathostomes. Both proteins showed structural and functional divergence, and shared evolutionary origin. Primary, secondary and tertiary sequences were compared to discover functional domains and conserved motifs in order to study the evolution of these two proteins. The structural and functional information relevant to evolutionary divergence was revealed using hydrophobic cluster analysis. Results: The findings demonstrate that two membrane proteins with only a small degree of sequence identity can have remarkably similar hydropathy profiles, pointing towards conserved and similar global structures. When facing the lipid bilayer or lining the pore lumen, the two proteins' aerolysin domains' corresponding residues displayed a similar and largely conserved pattern. Aerolysin-like proteins from different species can be identified using a fingerprint created by PIPSA analysis of the pore-forming protein. Conclusion: We were able to fully understand the mechanism of action during pore formation through structural studies of these proteins.

Funder

Deanship of Scientific Research (DSR) at King AbdulAziz University, Jeddah, Saudi Arabia

Publisher

Bentham Science Publishers Ltd.

Subject

Biochemistry,General Medicine,Structural Biology

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