Publications by authors named "Dev Aditya"

Article Synopsis
  • * The AI teacher conducted a 9-lesson course focusing on employability and transferable skills, with 207 students participating in the program.
  • * Results revealed a completion rate exceeding 47%, significant student engagement, and high satisfaction levels, highlighting the promise of AI virtual teachers in higher education compared to traditional MOOC platforms.
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Aim: In the present studies, we examine the construct validity and criterion-related validity of a previously unpublished, eight-item measure of relational wellbeing.

Methods: First, in two pre-COVID-Era pilot studies within the UK ('s = 207 and 146, respectively), results of exploratory factor analyses revealed that-with the possible exception of one item regarding close relationships-the items assessed individual differences along a single dimension (i.e.

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  • The main function of glutamyl-tRNA synthetase (GluRS) is to attach glutamate to tRNA, but not all bacterial GluRSs perform this function in the same way; some can glutamylate multiple tRNA types.
  • Research has indicated that specific mutations in GluRS and tRNA influence this specificity, with significant studies primarily based on E. coli GluRS despite differences in structure compared to non-proteobacterial GluRSs.
  • This study successfully analyzed the crystal structure of a mutant GluRS from E. coli and highlighted the importance of a specific loop on GluRS that interacts with the tRNA, revealing new insights into the mechanisms behind tRNA
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Phosphorylation is a key post-translational modification that alters the functional state of many proteins. The toxin HipA, which phosphorylates glutamyl-tRNA synthetase and triggers bacterial persistence under stress, becomes inactivated upon autophosphorylation of Ser150. Interestingly, Ser150 is phosphorylation-incompetent in the crystal structure of HipA since it is deeply buried ("in-state"), although in the phosphorylated state it is solvent exposed ("out-state").

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Interaction between human positive coactivator 4 (PC4), an abundant nuclear protein, and the tumor suppressor protein p53 plays a crucial role in initiating apoptosis. In certain neurodegenerative diseases PC4 assisted-p53-dependent apoptosis may play a central role. Thus, disruption of p53-PC4 interaction may be a good drug target for certain disease pathologies.

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Chlorogenic acid (CGA) is a phenolic compound with well-known antibacterial properties against pathogens. In this study, structural and biochemical characterization was used to show the inhibitory role of CGA against the enzyme of the shikimate pathway, a well-characterized drug target in several pathogens. Here, we report the crystal structures of dehydroquinate synthase (DHQS), the second enzyme of the shikimate pathway, from (DHQS), in binary complex with NAD and ternary complex with NAD and CGA.

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The first committed step of the shikimate pathway is catalyzed by a metalloenzyme 3-deoxy-d-arabino-heptulosonate-7-phosphate synthase (DAH7PS), which exhibits vulnerability to the oxidative stress. DAH7PS undergoes inactivation in multiple ways in the presence of redox metal, HO, and superoxide. The molecular mechanism and susceptibility of its inactivation might differ in different organisms and are presently unclear.

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Article Synopsis
  • DAHPS is the first enzyme in the shikimate pathway, crucial for synthesizing aromatic amino acids in microorganisms, making it a potential target for antimicrobial drug development.
  • The first structure of the AroQ class chorismate mutase (BsCM_2) from Bacillus subtilis was determined in complex with citrate and chlorogenic acid, revealing important details about ligand binding and active site flexibility.
  • Molecular dynamics show that certain conformational changes in the enzyme's structure may influence DAHPS regulation, highlighting chlorogenic acid's higher binding affinity compared to chorismate, which could aid in creating new antimicrobial therapies.
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Lipopolysaccharide (LPS) is an important surface component and a potential virulence factor in the pathogenesis of Gram-negative bacteria. UDP-N-acetylglucosamine acyltransferase (LpxA) enzyme catalyzes the first reaction of LPS biosynthesis, reversible transfer of R-3-hydroxy-acyl moiety from donor R-3-hydroxy-acyl-acyl carrier protein to the 3' hydroxyl position of UDP-N-acetyl-glucosamine. LpxA enzyme's essentiality in bacterial survival and absence of any homologous protein in humans makes it a promising target for anti-bacterial drug development.

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The glycosyl hydrolase 18 (GH18) family consists of active chitinases as well as chitinase like lectins/proteins (CLPs). The CLPs share significant sequence and structural similarities with active chitinases, however, do not display chitinase activity. Some of these proteins are reported to have specific functions and carbohydrate binding property.

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