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Decaprenyl-phosphoryl-ribose 2′-epimerase (DprE1): challenging target for antitubercular drug discovery

Overview of attention for article published in BMC Chemistry, June 2018
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Title
Decaprenyl-phosphoryl-ribose 2′-epimerase (DprE1): challenging target for antitubercular drug discovery
Published in
BMC Chemistry, June 2018
DOI 10.1186/s13065-018-0441-2
Pubmed ID
Authors

Jineetkumar Gawad, Chandrakant Bonde

Abstract

Tuberculosis has proved harmful to the entire history of mankind from past several decades. Decaprenyl-phosphoryl-ribose 2'-epimerase (DprE1) is a recent target which was identified in 2009 but unfortunately it is neither explored nor crossed phase II. In past several decades few targets were identified for effective antitubercular drug discovery. Resistance is the major problem for effective antitubercular drug discovery. Arabinose is constituent of mycobacterium cell wall. Biosynthesis of arabinose is FAD dependant two step epimerisation reaction which is catalysed by DprE1 and DprE2 flavoprotein enzymes. The current review is mainly emphases on DprE1 as a perspective challenge for further research.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 75 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 75 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 13 17%
Student > Master 8 11%
Student > Bachelor 8 11%
Researcher 6 8%
Other 3 4%
Other 9 12%
Unknown 28 37%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 14 19%
Chemistry 13 17%
Biochemistry, Genetics and Molecular Biology 8 11%
Engineering 3 4%
Medicine and Dentistry 3 4%
Other 5 7%
Unknown 29 39%