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Sökning: id:"swepub:oai:DiVA.org:kth-324391" > Molecular explorati...

Molecular explorations of the Leishmania donovani 6-phosphogluconolactonase enzyme, a key player in the pentose phosphate pathway

Dhumal, Tushar Tukaram (författare)
Natl Inst Pharmaceut Educ & Res, Dept Biotechnol, Mohali 160062, Punjab, India.,Department of Biotechnology, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali, Punjab, India
Kumar, Rajender (författare)
Umeå universitet,Institutionen för klinisk mikrobiologi,Umeå Univ, Dept Clin Microbiol, SE-90185 Umeå, Sweden.
Paul, Anindita (författare)
Natl Inst Pharmaceut Educ & Res, Dept Biotechnol, Mohali 160062, Punjab, India.,Department of Biotechnology, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali, Punjab, India
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Roy, Pradyot Kumar (författare)
Natl Inst Pharmaceut Educ & Res, Dept Biotechnol, Mohali 160062, Punjab, India.,Department of Biotechnology, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali, Punjab, India
Garg, Prabha (författare)
Natl Inst Pharmaceut Educ & Res, Dept Pharmacoinformat, Mohali 160062, Punjab, India.,Department of Pharmacoinformatics, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali, Punjab, India
Singh, Sushma (författare)
Natl Inst Pharmaceut Educ & Res, Dept Biotechnol, Mohali 160062, Punjab, India.,Department of Biotechnology, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali, Punjab, India
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Natl Inst Pharmaceut Educ & Res, Dept Biotechnol, Mohali 160062, Punjab, India Department of Biotechnology, National Institute of Pharmaceutical Education and Research, SAS Nagar, Mohali, Punjab, India (creator_code:org_t)
Elsevier BV, 2022
2022
Engelska.
Ingår i: Biochimie. - : Elsevier BV. - 0300-9084 .- 1638-6183. ; 202, s. 212-225
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The enzymes of the pentose phosphate pathway are vital to survival in kinetoplastids. The second step of the pentose phosphate pathway involves hydrolytic cleavage of 6-phosphogluconolactone to 6- phosphogluconic acid by 6-phosphogluconolactonase (6PGL). In the present study, Leishmania dono-vani 6PGL (Ld6PGL) was cloned and overexpressed in bacterial expression system. Comparative sequence analysis revealed the conserved sequence motifs, functionally and structurally important residues in 6PGL family. In silico amino acid substitution study and interacting partners of 6PGL were predicted. The Ld6PGL enzyme was found to be active in the assay and in the parasites. Specificity was confirmed by Western blot analysis. The similar to 30 kDa protein was found to be a dimer in MALDI, glutaraldehyde cross-linking and size exclusion chromatography studies. Kinetic analysis and structural stability studies of Ld6PGL were performed with denaturants and at varied temperature. Computational 3D Structural modelling of Ld6PGL elucidates that it has a similar a/b hydrolase fold structural topology as in other members of 6PGL family. The three loops are found in extended form when the structure is compared with the human 6PGL (Hs6PGL). Further, enzyme substrate binding mode and its mechanism were investigated using the molecular docking and molecular simulation studies. Interesting dynamics action of substrate 6-phosphogluconolactone was observed into active site during MD simulation. Interesting differences were observed between host and parasite enzyme which pointed towards its potential to be explored as an antileishmanial drug target. This study forms the basis for further analysis of the role of Ld6PGL in combating oxidative stress in Leishmania.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

Leishmania donovani
6-Phosphogluconolactonase
Pentose phosphate pathway
Molecular dynamics simulations
Human 6PGL

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