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References from Unraveling Cholesterol Catabolism in Mycobacterium tuberculosis : ChsE4-ChsE5 α2β2 Acyl-CoA Dehydrogenase Initiates β-Oxidation of 3-Oxo-cholest-4-en-26-oyl CoA. Local targets link to admitted publications; unresolved targets remain external evidence.
A thiolase of Mycobacterium tuberculosis is required for virulence and production of androstenedione and androstadienedione from cholesterol
10.1128/iai.00893-09 · 2010 · External reference
Studies of a ring-cleaving dioxygenase illuminate the role of cholesterol metabolism in the pathogenesis of Mycobacterium tuberculosis
10.1371/journal.ppat.1000344 · 2009 · External reference
Mycobacterial persistence requires the utilization of host cholesterol
10.1073/pnas.0711159105 · 2008 · External reference
igr Genes and Mycobacterium tuberculosis Cholesterol Metabolism
10.1128/jb.00452-09 · 2009 · External reference
Foamy macrophages from tuberculous patients’ granulomas constitute a nutrient-rich reservoir for M. tuberculosis persistence
10.1371/journal.ppat.1000204 · 2008 · External reference
The mechanism of microbial conversion of cholesterol into 17-keto steroids
10.1021/ja00984a039 · 1967 · External reference
Mechanisms of steroid oxidation by microorganisms 0.14. Pathway of cholesterol side-chain degradation
10.1021/bi00842a039 · 1968 · External reference
Peroxisomal β-oxidation and peroxisome proliferator-activated receptor α: An Adaptive Metabolic System
10.1146/annurev.nutr.21.1.193 · 2001 · External reference
Rv1106c from Mycobacterium tuberculosis Is a 3β-Hydroxysteroid Dehydrogenase
10.1021/bi700688x · 2007 · External reference
Mycobacterial Cytochrome P450 125 (Cyp125) Catalyzes the Terminal Hydroxylation of C27 Steroids
10.1074/jbc.m109.072132 · 2009 · External reference
Functional redundancy of steroid C26-monooxygenase activity in Mycobacterium tuberculosis revealed by biochemical and genetic analyses
10.1074/jbc.m110.161117 · 2010 · External reference
Mycobacterium tuberculosis CYP125A1, a steroid C27 monooxygenase that detoxifies intracellularly generated cholest-4-en-3-one
10.1111/j.1365-2958.2010.07243.x · 2010 · External reference
FadD19 of Rhodococcus rhodochrous DSM43269, a steroid-coenzyme A ligase essential for degradation of C-24 branched sterol side chains
10.1128/aem.00380-11 · 2011 · External reference
Actinobacterial acyl coenzyme A synthetases involved in steroid side-chain catabolism
10.1128/jb.01012-13 · 2014 · External reference
A gene cluster encoding cholesterol catabolism in a soil actinomycete provides insight into Mycobacterium tuberculosis survival in macrophages
10.1073/pnas.0605728104 · 2007 · External reference
Acyl-CoA dehydrogenases. A mechanistic overview
10.1046/j.1432-1033.2003.03946.x · 2004 · External reference
Pathway Profiling in Mycobacterium tuberculosis: Elucidation of a cholesterol-derived catabolite and the enzymes that catalyze its metabolism
10.1074/jbc.m111.313643 · 2011 · External reference
Mycobacterium tuberculosis utilizes a unique heterotetrameric structure for dehydrogenation of the cholesterol side chain
10.1021/bi4002979 · 2013 · External reference
A Distinct MaoC-like enoyl-CoA hydratase architecture mediates cholesterol catabolism in Mycobacterium tuberculosis
10.1021/cb500232h · 2014 · External reference
Shrinking the FadE proteome of Mycobacterium tuberculosis: Insights into cholesterol metabolism through identification of an α2β2 heterotetrameric acyl coenzyme A dehydrogenase family
10.1128/jb.00502-13 · 2013 · External reference
A highly conserved transcriptional repressor controls a large regulon involved in lipid degradation in Mycobacterium smegmatis and Mycobacterium tuberculosis
10.1111/j.1365-2958.2007.05827.x · 2007 · External reference
Identification of gene expression profiles in the actinomycete Gordonia neofelifaecis grown with different steroids
10.1139/gen-2014-0030 · 2014 · External reference
Cholesterol utilization in mycobacteria is controlled by two TetR-type transcriptional regulators: kstR and kstR2
10.1099/mic.0.034538-0 · 2010 · External reference
Acyl-CoA dehydrogenases and acyl-CoA oxidases. Structural basis for mechanistic similarities and differences
10.1046/j.1432-1033.2003.03948.x · 2004 · External reference
An efficient synthesis of 25-hydroxycholesterol from stigmasterol
10.1016/s0040-4039(01)93251-4 · 1977 · External reference
A simple and highly stereoselective route to E-α,β-unsaturated aldehydes
10.1021/jo00061a027 · 1993 · External reference
Crystal structure determination of cholesterol oxidase from Streptomyces and structural characterization of key active site mutants
10.1021/bi982497j · 1999 · External reference
FadA5 a thiolase from Mycobacterium tuberculosis – a unique steroid-binding pocket reveals the potential for drug development against tuberculosis
10.1016/j.str.2014.10.010 · 2014 · External reference
An acyl-coenzyme A dehydrogenase assay utilizing the ferricenium ion
10.1016/0003-2697(90)90080-s · 1990 · External reference
Stereochemistry of peroxisomal and mitochondrial beta-oxidation of alpha-methylacyl-CoAs
10.1111/j.1432-1033.1997.00434.x · 1997 · External reference
Regel zur Abschatzung der Chemischen Verschiebung von Protonen an einer Doppelbindung
10.1002/hlca.660490122 · 1966 · External reference
Linking crystallographic model and data quality
10.1126/science.1218231 · 2012 · External reference
Crystal structures of medium-chain acyl-CoA dehydrogenase from pig liver mitochondria with and without substrate
10.1073/pnas.90.16.7523 · 1993 · External reference
CAVER Analyst 1.0: graphic tool for interactive visualization and analysis of tunnels and channels in protein structures
10.1093/bioinformatics/btu364 · 2014 · External reference
Identification of Mycobacterial genes that alter growth and pathology in macrophages and in mice
10.1086/520089 · 2007 · External reference
Absolute metabolite concentrations and implied enzyme active site occupancy in Escherichia coli
10.1038/nchembio.186 · 2009 · External reference
Pathogen roid rage: Cholesterol utilization by Mycobacterium tuberculosis
10.3109/10409238.2014.895700 · 2014 · External reference
Correlated single-crystal electronic absorption spectroscopy and X-ray crystallography at NSLS beamline X26-C
10.1107/s0909049511006315 · 2011 · External reference
XDS
10.1107/s0907444909047337 · 2010 · External reference
How good are my data and what is the resolution?
10.1107/s0907444913000061 · 2013 · External reference
Data processing and analysis with the autoPROC toolbox
10.1107/s0907444911007773 · 2011 · External reference
Substructure solution with SHELXD
10.1107/s0907444902011678 · 2002 · External reference
Jolly SAD
10.1107/s090744490200118x · 2002 · External reference
Automated Structure Solution with autoSHARP
2007 · External reference
Methods used in the structure determination of bovine mitochondrial F1 ATPase
10.1107/s0907444995008754 · 1996 · External reference
The Buccaneer software for automated model building. 1. Tracing protein chains
10.1107/s0907444906022116 · 2006 · External reference
Recent developments in classical density modification
10.1107/s090744490903947x · 2010 · External reference
Features and development of Coot
10.1107/s0907444910007493 · 2010 · External reference
REFMAC5 for the refinement of macromolecular crystal structures
10.1107/s0907444911001314 · 2011 · External reference
Automated Structure Solution with the PHENIX Suite
10.1007/978-1-60327-058-8_28 · 2008 · External reference
MolProbity: all-atom structure validation for macromolecular crystallography
10.1107/s0907444909042073 · 2010 · External reference
Integrated software for macromolecular crystallography synchrotron beamlines II: revision, robots and a database
10.1107/s0907444906030162 · 2006 · External reference
Biomolecular solution X-ray scattering at the National Synchrotron Light Source
10.1107/s0909049510036022 · 2011 · External reference
