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http://purl.uniprot.org/citations/17389997http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17389997http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17389997http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Citation
http://purl.uniprot.org/citations/17389997http://www.w3.org/2000/01/rdf-schema#comment"The cell envelope of Mycobacterium tuberculosis (Mtb) is a treasure house of a variety of biologically active molecules with fascinating architectures. The decoding of the genetic blueprint of Mtb in recent years has provided the impetus for dissecting the metabolic pathways involved in the biosynthesis of lipidic metabolites. The focus of the Highlight is to emphasize the functional role of polyketide synthase (PKS) proteins in the biosynthesis of complex mycobacterial lipids. The catalytic as well as mechanistic versatility of PKS. in generating metabolic diversity and the significance of recently discovered fatty acyl-AMP ligases in establishing "biochemical crosstalk" between fatty acid synthases (FASs) and PKSs is described. The phenotypic heterogeneity and remodeling of the mycobacterial cell wall in its aetiopathogenesis is discussed."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.org/dc/terms/identifier"doi:10.1039/b616817p"xsd:string
http://purl.uniprot.org/citations/17389997http://purl.org/dc/terms/identifier"doi:10.1039/b616817p"xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/author"Gokhale R.S."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/author"Gokhale R.S."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/author"Mohanty D."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/author"Mohanty D."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/author"Saxena P."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/author"Saxena P."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/author"Chopra T."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/author"Chopra T."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/name"Nat. Prod. Rep."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/name"Nat. Prod. Rep."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/pages"267-277"xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/pages"267-277"xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/title"Versatile polyketide enzymatic machinery for the biosynthesis of complex mycobacterial lipids."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/title"Versatile polyketide enzymatic machinery for the biosynthesis of complex mycobacterial lipids."xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/volume"24"xsd:string
http://purl.uniprot.org/citations/17389997http://purl.uniprot.org/core/volume"24"xsd:string
http://purl.uniprot.org/citations/17389997http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/17389997