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Structural exploration of glutamine synthetase from Leishmania donovani: Insights from in silico and in vitro analysis.
Kumar, Vinay; Sushma Sri, N; Tripathi, Neha; Sharma, Vishnu K; Bharatam, Prasad V; Garg, Prabha; Singh, Sushma.
Afiliação
  • Kumar V; Department of Biotechnology, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali 160062, Punjab, India.
  • Sushma Sri N; Department of Biotechnology, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali 160062, Punjab, India.
  • Tripathi N; Department of Pharmacoinformatics, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali 160062, Punjab, India; CEISAM, UMR CNRS 6230, BP 92208, 2 Rue de la Houssinière, 44322 Nantes Cedex 3, France(1).
  • Sharma VK; Department of Pharmacoinformatics, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali 160062, Punjab, India.
  • Bharatam PV; Department of Pharmacoinformatics, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali 160062, Punjab, India; Department of Medicinal Chemistry National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali 160062, Punjab, India.
  • Garg P; Department of Pharmacoinformatics, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali 160062, Punjab, India.
  • Singh S; Department of Biotechnology, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali 160062, Punjab, India. Electronic address: sushmasingh@niper.ac.in.
Int J Biol Macromol ; 146: 860-874, 2020 Mar 01.
Article em En | MEDLINE | ID: mdl-31726137
Glutamine synthetase from L. donovani (LdGS) has been identified as a potential antileishmanial target in our previous report based on biochemical and inhibition studies. With the aim to structurally explore LdGS, systematic in silico and in vitro studies have been employed in the present study to identify amino acids crucial for LdGS mediated catalysis. A comparative analysis with human GS (HsGS) was performed which revealed significant differences in the active site pocket of human and parasite GS enzyme. The important amino acids identified from the in silico analysis of the optimized complexes, were subjected to in silico and in vitro alanine scanning by site directed mutagenesis. The results indicated crucial conserved and non conserved residues required for GS activity. The role of these residues in maintenance of secondary and tertiary structure of GS enzyme was also explored. In silico virtual screening was performed which resulted in the identification of five hits i.e. ZINC83236243, ZINC77319454, ZINC83236244, ZINC83236734 and ZINC83236736, as potential LdGS selective inhibitors. The illustrated structural and functional details of enzyme provides a better understanding of the structural integrity of LdGS and can be further utilized for the development of parasite specific GS inhibitors for treatment of visceral leishmaniasis infections.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leishmania donovani / Simulação por Computador / Glutamato-Amônia Ligase Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leishmania donovani / Simulação por Computador / Glutamato-Amônia Ligase Idioma: En Ano de publicação: 2020 Tipo de documento: Article