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Lehmann, J.* ; Vomacka, J.* ; Esser, K. ; Nodwell, M.* ; Kolbe, K.* ; Raemer, P.* ; Protzer, U. ; Reiling, N.* ; Sieber, S.A.*

Human lysosomal acid lipase inhibitor lalistat impairs Mycobacterium tuberculosis growth by targeting bacterial hydrolases.

MedChemComm 7, 1797-1801 (2016)
Publ. Version/Full Text Research data DOI
Open Access Gold (Paid Option)
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Lalistat inhibits growth of Mycobacterium tuberculosis in bacterial culture as well as in infected macrophages. Target identification by quantitative proteomics revealed a cluster of 20 hydrolytic proteins including members of the lipase family. Lipases are essential for M. tuberculosis fatty acid production and energy storage thus representing promising antibiotic targets.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords 1,3-dipolar Cycloadditions; Pancreatic Lipase; Terminal Alkynes; In-vitro; Tetrahydrolipstatin; Metabolism; Susceptibility; Lipstatin; Pathogen; Dormancy
ISSN (print) / ISBN 2040-2511
e-ISSN 2040-2503
Journal MedChemComm
Quellenangaben Volume: 7, Issue: 9, Pages: 1797-1801 Article Number: , Supplement: ,
Publisher Royal Society of Chemistry (RSC)
Publishing Place Cambridge
Non-patent literature Publications
Reviewing status Peer reviewed