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Vinay Kumar Nandicoori

Researcher at International Centre for Genetic Engineering and Biotechnology

Publications -  64
Citations -  1909

Vinay Kumar Nandicoori is an academic researcher from International Centre for Genetic Engineering and Biotechnology. The author has contributed to research in topics: Mycobacterium tuberculosis & Phosphorylation. The author has an hindex of 25, co-authored 54 publications receiving 1569 citations.

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Mycobacteria modulate host epigenetic machinery by Rv1988 methylation of a non-tail arginine of histone H3

TL;DR: It is shown that Rv1988, a secreted mycobacterial protein, is a functional methyltransferase that localizes to the host nucleus and interacts with chromatin that methylates histone H3 at H3R42 and represses the genes involved in the first line of defence againstMycobacteria.
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PknB-mediated phosphorylation of a novel substrate, N-acetylglucosamine-1-phosphate uridyltransferase, modulates its acetyltransferase activity.

TL;DR: It is demonstrated that although PknB-mediated phosphorylation of GlmU does not affect its uridyl transferase activity, it significantly modulates the acetyltransferase activity.
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Peptide−Sugar Ligation Catalyzed by Transpeptidase Sortase: A Facile Approach to Neoglycoconjugate Synthesis

TL;DR: A novel enzymatic method involving an unprecedented sortase-catalyzed transamidation reaction for site-specific engineering of sugars into native proteins and it is shown that sugars appended with a 6-aminohexose moiety can be efficiently ligated to peptides and proteins encoded with a LPXTG sortase recognition sequence.
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Protein Kinase B (PknB) of Mycobacterium tuberculosis Is Essential for Growth of the Pathogen in Vitro as well as for Survival within the Host

TL;DR: The present study describes the comprehensive analysis of different domains of PknB in the context of viability in avirulent and virulent mycobacteria, finding stringent regulation of P KnB expression necessary for cell survival, with depletion or overexpression of PKnB leading to cell death.
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The interaction of mycobacterial protein Rv2966c with host chromatin is mediated through non-CpG methylation and histone H3/H4 binding

TL;DR: This is the first study that identifies a protein from a pathogenic bacteria with potential to influence host DNA methylation in a non-canonical manner providing the pathogen with a novel mechanism to alter the host epigenetic machinery.