A thiolase of Mycobacterium tuberculosis is required for virulence and production of androstenedione and androstadienedione from cholesterol.
about
High-resolution phenotypic profiling defines genes essential for mycobacterial growth and cholesterol catabolismPathogen roid rage: cholesterol utilization by Mycobacterium tuberculosisMycobacterium tuberculosis utilizes a unique heterotetrameric structure for dehydrogenation of the cholesterol side chainMycobacterium tuberculosis CYP125A1, a steroid C27 monooxygenase that detoxifies intracellularly generated cholest-4-en-3-oneA flavin-dependent monooxygenase from Mycobacterium tuberculosis involved in cholesterol catabolismActivity of 3-ketosteroid 9α-hydroxylase (KshAB) indicates cholesterol side chain and ring degradation occur simultaneously in Mycobacterium tuberculosisMycobacterial cytochrome p450 125 (cyp125) catalyzes the terminal hydroxylation of c27 steroidsMycobacterium tuberculosis: success through dormancyCrystal Structure of a Monomeric Thiolase-Like Protein Type 1 (TLP1) from Mycobacterium smegmatisA highly conserved mycobacterial cholesterol catabolic pathwaySubstrate Specificities and Conformational Flexibility of 3-Ketosteroid 9α-HydroxylasesMycobacterial genes essential for the pathogen's survival in the hostShrinking the FadE proteome of Mycobacterium tuberculosis: insights into cholesterol metabolism through identification of an α2β2 heterotetrameric acyl coenzyme A dehydrogenase familyCholesterol catabolism by Mycobacterium tuberculosis requires transcriptional and metabolic adaptationsFunctional redundancy of steroid C26-monooxygenase activity in Mycobacterium tuberculosis revealed by biochemical and genetic analysesPathway profiling in Mycobacterium tuberculosis: elucidation of cholesterol-derived catabolite and enzymes that catalyze its metabolismCholesterol utilization in mycobacteria is controlled by two TetR-type transcriptional regulators: kstR and kstR2The Mycobacterium tuberculosis regulatory network and hypoxiaUnraveling Cholesterol Catabolism in Mycobacterium tuberculosis: ChsE4-ChsE5 α2β2 Acyl-CoA Dehydrogenase Initiates β-Oxidation of 3-Oxo-cholest-4-en-26-oyl CoA.The Structure of the Transcriptional Repressor KstR in Complex with CoA Thioester Cholesterol Metabolites Sheds Light on the Regulation of Cholesterol Catabolism in Mycobacterium tuberculosis.Metabolic Perspectives on PersistenceCatabolism and biotechnological applications of cholesterol degrading bacteria.Anoxic androgen degradation by the denitrifying bacterium Sterolibacterium denitrificans via the 2,3-seco pathwayImproving the production of 22-hydroxy-23,24-bisnorchol-4-ene-3-one from sterols in Mycobacterium neoaurum by increasing cell permeability and modifying multiple genesRv3723/LucA coordinates fatty acid and cholesterol uptake in Mycobacterium tuberculosis.Mycobacterium tuberculosis wears what it eatsMicrobial steroid transformations: current state and prospects.Statins increase rifampin mycobactericidal effect.A high-resolution network model for global gene regulation in Mycobacterium tuberculosis.The role of 3-ketosteroid 1(2)-dehydrogenase in the pathogenicity of Mycobacterium tuberculosis.Cholesterol is not an essential source of nutrition for Mycobacterium tuberculosis during infectionInhibition of the M. tuberculosis 3β-hydroxysteroid dehydrogenase by azasteroids.FadA5 a thiolase from Mycobacterium tuberculosis: a steroid-binding pocket reveals the potential for drug development against tuberculosisCholesterol oxidase is indispensable in the pathogenesis of Mycobacterium tuberculosisCholesterol catabolism as a therapeutic target in Mycobacterium tuberculosis.The tuberculosis drug discovery and development pipeline and emerging drug targets.Global analyses of TetR family transcriptional regulators in mycobacteria indicates conservation across species and diversity in regulated functionsMetabolic modeling predicts metabolite changes in Mycobacterium tuberculosis.The Essential Role of Cholesterol Metabolism in the Intracellular Survival of Mycobacterium leprae Is Not Coupled to Central Carbon Metabolism and Energy Production.Detection of a Putative TetR-Like Gene Related to Mycobacterium bovis BCG Growth in Cholesterol Using a gfp-Transposon Mutagenesis System.
P2860
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P2860
A thiolase of Mycobacterium tuberculosis is required for virulence and production of androstenedione and androstadienedione from cholesterol.
description
2009 nî lūn-bûn
@nan
2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@ast
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@en
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@nl
type
label
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@ast
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@en
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@nl
prefLabel
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@ast
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@en
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@nl
P2093
P2860
P356
P1476
A thiolase of Mycobacterium tu ...... tadienedione from cholesterol.
@en
P2093
Eugenie Dubnau
Irina Kolesnikova
Issar Smith
Natasha M Nesbitt
Patricia Fontán
Xinxin Yang
P2860
P304
P356
10.1128/IAI.00893-09
P407
P577
2009-10-12T00:00:00Z