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Publications

Design, Synthesis, and Structural Analysis of Cladosporin-Based Inhibitors of Malaria Parasites

Babbar P. et al, (2021), ACS Infectious Diseases

Drosophila OTK Is a Glycosaminoglycan-Binding Protein with High Conformational Flexibility

Rozbesky D. et al, (2020), Structure, 28, 507 - 515.e5

Diversity of oligomerization in Drosophila semaphorins suggests a mechanism of functional fine-tuning

Rozbesky D. et al, (2019), Nature Communications, 10

Semaphorin 3A induces cytoskeletal paralysis in tumor-specific CD8+ T cells

Barnkob MB. et al, (2019)

Assessing nipah related internet activity behaviour in india: An insight from analytical search volumes of google trends

Chahar P. et al, (2019), Indian Journal of Forensic Medicine and Toxicology, 13, 282 - 287

Conformational changes in glutaminyl-tRNA synthetases upon binding of the substrates and analogs using molecular docking and molecular dynamics approaches

Nachiappan M. et al, (2019), Journal of Biomolecular Structure and Dynamics, 1 - 15

Author Correction: Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding

Walters LC. et al, (2018), Nature Communications, 9

Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding

Walters LC. et al, (2018), Nature Communications, 9

Structural and functional analysis of Glutaminyl-tRNA synthetase (TtGlnRS) from Thermus thermophilus HB8 and its complexes

Nachiappan M. et al, (2018), International Journal of Biological Macromolecules, 120, 1379 - 1386

Structure of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase–dihydropteroate synthase from Plasmodium vivax sheds light on drug resistance

Yogavel M. et al, (2018), Journal of Biological Chemistry, 293, 14962 - 14972

Drug targeting of one or more aminoacyl-tRNA synthetase in the malaria parasite Plasmodium falciparum

Manickam Y. et al, (2018), Drug Discovery Today, 23, 1233 - 1240

Targeting Prolyl-tRNA Synthetase to Accelerate Drug Discovery against Malaria, Leishmaniasis, Toxoplasmosis, Cryptosporidiosis, and Coccidiosis

Jain V. et al, (2017), Structure, 25, 1495 - 1505.e6

Structure-Based Targeting of Orthologous Pathogen Proteins Accelerates Antiparasitic Drug Discovery

Jain V. et al, (2017), ACS Infectious Diseases, 3, 281 - 292

Repurposing of Potent Drug Candidates for Multiparasite Targeting

Jain V. and Sharma A., (2017), Trends in Parasitology, 33, 158 - 161

Dimerization of Arginyl-tRNA Synthetase by Free Heme Drives Its Inactivation in Plasmodium falciparum

Jain V. et al, (2016), Structure, 24, 1476 - 1487

Structure of Prolyl-tRNA Synthetase-Halofuginone Complex Provides Basis for Development of Drugs against Malaria and Toxoplasmosis

Jain V. et al, (2015), Structure, 23, 819 - 829

Structural and functional analysis of the anti-malarial drug target prolyl-tRNA synthetase

Jain V. et al, (2014), Journal of Structural and Functional Genomics, 15, 181 - 190

Detection of Mycobacterium tuberculosis GlcB or HspX Antigens or devR DNA Impacts the Rapid Diagnosis of Tuberculous Meningitis in Children

Haldar S. et al, (2012), PLoS ONE, 7, e44630 - e44630

Include forthcoming?