Harnessing immunoinformatics for precision vaccines: designing epitope-based subunit vaccines against hepatitis E virus

EK Oladipo, EO Dairo, CO Bamigboye, AF Ajayi… - …, 2024 - mdpi.com
Background/Objectives: Hepatitis E virus (HEV) is an RNA virus recognized to be spread
mainly by fecal-contaminated water. Its infection is known to be a serious threat to public …

[HTML][HTML] In silico structural and functional annotation of hypothetical proteins of Vibrio cholerae O139

MS Islam, SM Shahik, M Sohel, NIA Patwary… - Genomics & …, 2015 - ncbi.nlm.nih.gov
In develo** countries threat of cholera is a significant health concern whenever water
purification and sewage disposal systems are inadequate. Vibrio cholerae is one of the …

In Silico Screening of Isocitrate Lyase for Novel Anti-Buruli Ulcer Natural Products Originating from Africa

SK Kwofie, B Dankwa, EA Odame, FE Agamah… - Molecules, 2018 - mdpi.com
Buruli ulcer (BU) is caused by Mycobacterium ulcerans and is predominant in both tropical
and subtropical regions. The neglected debilitating disease is characterized by chronic …

Molecular-docking study of malaria drug target enzyme transketolase in Plasmodium falciparum 3D7 portends the novel approach to its treatment

MA Hasan, MHH Mazumder, AS Chowdhury… - Source code for biology …, 2015 - Springer
Background Malaria has been a major life threatening mosquito borne disease from long
since. Unavailability of any effective vaccine and recent emergence of multi drug resistant …

A comprehensive immunoinformatics and target site study revealed the corner-stone toward Chikungunya virus treatment

MA Hasan, MA Khan, A Datta, MHH Mazumder… - Molecular …, 2015 - Elsevier
Recent concerning facts of Chikungunya virus (CHIKV); a Togaviridae family alphavirus has
proved this as a worldwide emerging threat which causes Chikungunya fever and …

Synthesis, in vitro α-glucosidase, α-amylase inhibitory potential and molecular docking study of thiadiazole-sulfonamide hybrid analogues

H Ullah, N Nadeem, F Rahim, A Nawaz… - Chemical Data …, 2023 - Elsevier
We have synthesized fourteen thiadiazole-sulfonamide hybrid analogues (1–14),
characterized throygh different technequies ie, NMR, HR-EIMS, and screened against α …

Identification of putative drug targets in Vancomycin-resistant Staphylococcus aureus (VRSA) using computer aided protein data analysis

MA Hasan, MA Khan, T Sharmin, MHH Mazumder… - Gene, 2016 - Elsevier
Vancomycin-resistant Staphylococcus aureus (VRSA) is a Gram-positive, facultative aerobic
bacterium which is evolved from the extensive exposure of Vancomycin to Methicillin …

Binding free energy calculations of nine FDA‐approved protease inhibitors against HIV‐1 subtype C I36T↑ T containing 100 amino acids per monomer

HA Lockhat, JRA Silva, CN Alves… - Chemical biology & …, 2016 - Wiley Online Library
In this work, have investigated the binding affinities of nine FDA‐approved protease inhibitor
drugs against a new HIV‐1 subtype C mutated protease, I36T↑ T. Without an X‐ray crystal …

Structure and function insights garnered from in silico modeling of the thrombospondin type‐1 domain‐containing 7A antigen

SV Stoddard, CL Welsh, MM Palopoli… - Proteins: Structure …, 2019 - Wiley Online Library
The thrombospondin type‐1 domain containing 7A (THSD7A) protein is known to be one of
the antigens responsible for the autoimmune disorder idiopathic membranous nephropathy …

Computational Analysis and Binding Site Identification of Type III Secretion System ATPase from Pseudomonas aeruginosa

R Dash, SMZ Hosen, T Sultana, M Junaid… - Interdisciplinary …, 2016 - Springer
In many gram-negative bacteria, the type III secretion system (T3SS), as a virulence factor, is
an attractive target for develo** novel antibacterial. Regarding this, in our study, we aimed …