Molecular modeling studies of Fatty acyl-CoA synthetase (FadD13) from Mycobacterium tuberculosis--a potential target for the development of antitubercular drugs.
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Computational databases, pathway and cheminformatics tools for tuberculosis drug discovery.Targeting Mycobacterium tuberculosis Tumor Necrosis Factor Alpha-Downregulating Genes for the Development of Antituberculous Vaccines.Cyclic AMP-dependent protein lysine acylation in mycobacteria regulates fatty acid and propionate metabolism.Systematic Identification of Mycobacterium tuberculosis Effectors Reveals that BfrB Suppresses Innate Immunity.Docking and molecular dynamics studies of peptide inhibitors of ornithine decarboxylase: a rate-limiting enzyme for the metabolism of Fusarium solani.Genome-based approaches to develop epitope-driven subunit vaccines against pathogens of infective endocarditis.
P2860
Molecular modeling studies of Fatty acyl-CoA synthetase (FadD13) from Mycobacterium tuberculosis--a potential target for the development of antitubercular drugs.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
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name
Molecular modeling studies of ...... pment of antitubercular drugs.
@en
type
label
Molecular modeling studies of ...... pment of antitubercular drugs.
@en
prefLabel
Molecular modeling studies of ...... pment of antitubercular drugs.
@en
P2093
P2860
P1476
Molecular modeling studies of ...... pment of antitubercular drugs.
@en
P2093
Anil K Tyagi
Garima Khare
Narayanan Latha
Nidhi Jatana
Sarvesh Jangid
P2860
P2888
P304
P356
10.1007/S00894-010-0727-3
P577
2010-05-08T00:00:00Z