Exploring the substrate promiscuity of an antibiotic inactivating enzyme-Reference-Cited by-同舟云学术

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Exploring the substrate promiscuity of an antibiotic inactivating enzyme

Published:2014 Issue:10 Volume:5 Page:1567-1570
ISSN:2040-2503
Container-title:Med. Chem. Commun.
language:en
Short-container-title:Med. Chem. Commun.

Author:

Agarwal Vinayak¹²³,Vondenhoff Gaston⁴⁵⁶,Gadakh Bharat⁴⁵⁶,Severinov Konstantin⁷⁸⁹¹⁰¹¹,Van Aerschot Arthur⁴⁵⁶,Nair Satish K.¹²³

Affiliation:

1. Center for Biophysics and Computational Biology and Institute for Genomic Biology

2. University of Illinois at Urbana Champaign

3. USA

4. Rega Institute for Medical Research, Medicinal Chemistry

5. KU Leuven

6. Belgium

7. Saint Petersburg State Polytechnical University

8. St. Petersburg, Russia

9. Institute of Molecular Genetics

10. Russian Academy of Sciences

11. Moscow, Russia

Abstract

Peptide–nucleotide conjugates have been extensively studied as scaffolds for the development of new antibiotics.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pharmaceutical Science,Biochemistry,Drug Discovery,Molecular Medicine,Pharmacology,Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/MD/C4MD00204K

Reference20 articles.

1. Recent advances in siderophore biosynthesis

2. Microcin C: biosynthesis and mechanisms of bacterial resistance

3. Aminoacyl tRNA synthetases as targets for antibiotic development

4. Major Biocontrol of Plant Tumors Targets tRNA Synthetase

5. Plant tumour biocontrol agent employs a tRNA-dependent mechanism to inhibit leucyl-tRNA synthetase

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1. Acylated sulfonamide adenosines as potent inhibitors of the adenylate-forming enzyme superfamily;European Journal of Medicinal Chemistry;2019-07

2. Comparative analysis of pyrimidine substituted aminoacyl-sulfamoyl nucleosides as potential inhibitors targeting class I aminoacyl-tRNA synthetases;European Journal of Medicinal Chemistry;2019-07

3. Synthesis of and triplex formation in oligonucleotides containing 2′-deoxy-6-thioxanthosine;Bioorganic & Medicinal Chemistry;2018-07

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