Literature DB >> 16904376

Novel targets for tuberculosis drug discovery.

Khisimuzi Mdluli1, Melvin Spigelman.   

Abstract

Since the determination of the Mycobacterium tuberculosis genome sequence, various groups have used the genomic information to identify and validate targets as the basis for the development of new anti-tuberculosis agents. Validation might include many components: demonstration of the biochemical activity of the enzyme, determination of its crystal structure in complex with an inhibitor or a substrate, confirmation of essentiality, and the identification of potent growth inhibitors either in vitro or in an infection model. If novel target validation and subsequent inhibition are matched by an improved understanding of disease biology, then new antibiotics could have the potential to shorten the duration of therapy, prevent resistance development and eliminate latent disease.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16904376     DOI: 10.1016/j.coph.2006.06.004

Source DB:  PubMed          Journal:  Curr Opin Pharmacol        ISSN: 1471-4892            Impact factor:   5.547


  34 in total

1.  Molecular modeling studies of Fatty acyl-CoA synthetase (FadD13) from Mycobacterium tuberculosis--a potential target for the development of antitubercular drugs.

Authors:  Nidhi Jatana; Sarvesh Jangid; Garima Khare; Anil K Tyagi; Narayanan Latha
Journal:  J Mol Model       Date:  2010-05-08       Impact factor: 1.810

2.  Spectroscopic studies on the [4Fe-4S] cluster in adenosine 5'-phosphosulfate reductase from Mycobacterium tuberculosis.

Authors:  Devayani P Bhave; Jiyoung A Hong; Michael Lee; Wei Jiang; Carsten Krebs; Kate S Carroll
Journal:  J Biol Chem       Date:  2010-11-12       Impact factor: 5.157

3.  A systems chemical biology study of malate synthase and isocitrate lyase inhibition in Mycobacterium tuberculosis during active and NRP growth.

Authors:  Elebeoba E May; Andrei Leitão; Alexander Tropsha; Tudor I Oprea
Journal:  Comput Biol Chem       Date:  2013-09-04       Impact factor: 2.877

4.  Deciphering the role of histidine 252 in mycobacterial adenosine 5'-phosphosulfate (APS) reductase catalysis.

Authors:  Jiyoung A Hong; Kate S Carroll
Journal:  J Biol Chem       Date:  2011-06-14       Impact factor: 5.157

5.  Structural basis for the broad substrate specificity of two acyl-CoA dehydrogenases FadE5 from mycobacteria.

Authors:  Xiaobo Chen; Jiayue Chen; Bing Yan; Wei Zhang; Luke W Guddat; Xiang Liu; Zihe Rao
Journal:  Proc Natl Acad Sci U S A       Date:  2020-06-29       Impact factor: 11.205

6.  Withdrawn

Authors: 
Journal:  Infect Disord Drug Targets       Date:  2012-11-16

Review 7.  Protein targets for structure-based anti-Mycobacterium tuberculosis drug discovery.

Authors:  Zhiyong Lou; Xiaoxue Zhang
Journal:  Protein Cell       Date:  2010-06-04       Impact factor: 14.870

8.  Targeting the chromosome partitioning protein ParA in tuberculosis drug discovery.

Authors:  Shahista Nisa; Marian C J Blokpoel; Brian D Robertson; Joel D A Tyndall; Shichun Lun; William R Bishai; Ronan O'Toole
Journal:  J Antimicrob Chemother       Date:  2010-09-01       Impact factor: 5.790

9.  Pathway-selective sensitization of Mycobacterium tuberculosis for target-based whole-cell screening.

Authors:  Garth L Abrahams; Anuradha Kumar; Suzana Savvi; Alvin W Hung; Shijun Wen; Chris Abell; Clifton E Barry; David R Sherman; Helena I M Boshoff; Valerie Mizrahi
Journal:  Chem Biol       Date:  2012-07-27

10.  Screening essential genes of Mycobacterium tuberculosis with the pathway enrichment method.

Authors:  Guangyu Xu; Zhaohui Ni; Yue Shi; Xiaoyu Sun; Huaidong Wang; Chengguo Wei; Guoqing Wang; Fan Li
Journal:  Mol Biol Rep       Date:  2014-08-07       Impact factor: 2.316

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.