These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
22. Mycobacterial sulfolipid shows a virulence by inhibiting cord factor induced granuloma formation and TNF-alpha release. Okamoto Y; Fujita Y; Naka T; Hirai M; Tomiyasu I; Yano I Microb Pathog; 2006 Jun; 40(6):245-53. PubMed ID: 16626929 [TBL] [Abstract][Full Text] [Related]
23. Identification, function and structure of the mycobacterial sulfotransferase that initiates sulfolipid-1 biosynthesis. Mougous JD; Petzold CJ; Senaratne RH; Lee DH; Akey DL; Lin FL; Munchel SE; Pratt MR; Riley LW; Leary JA; Berger JM; Bertozzi CR Nat Struct Mol Biol; 2004 Aug; 11(8):721-9. PubMed ID: 15258569 [TBL] [Abstract][Full Text] [Related]
24. Molecular cloning and expression of a novel glycolipid sulfotransferase in Mycobacterium tuberculosis. Rivera-Marrero CA; Ritzenthaler JD; Newburn SA; Roman J; Cummings RD Microbiology (Reading); 2002 Mar; 148(Pt 3):783-792. PubMed ID: 11882713 [TBL] [Abstract][Full Text] [Related]
25. Sulfolipid accumulation in Mycobacterium tuberculosis disrupted in the mce2 operon. Marjanovic O; Iavarone AT; Riley LW J Microbiol; 2011 Jun; 49(3):441-7. PubMed ID: 21717330 [TBL] [Abstract][Full Text] [Related]
26. Mycobacterial phenolic glycolipid virulence factor biosynthesis: mechanism and small-molecule inhibition of polyketide chain initiation. Ferreras JA; Stirrett KL; Lu X; Ryu JS; Soll CE; Tan DS; Quadri LE Chem Biol; 2008 Jan; 15(1):51-61. PubMed ID: 18158259 [TBL] [Abstract][Full Text] [Related]
27. The ppm operon is essential for acylation and glycosylation of lipoproteins in Corynebacterium glutamicum. Mohiman N; Argentini M; Batt SM; Cornu D; Masi M; Eggeling L; Besra G; Bayan N PLoS One; 2012; 7(9):e46225. PubMed ID: 23029442 [TBL] [Abstract][Full Text] [Related]
28. Characterization of sulfolipids of Mycobacterium tuberculosis H37Rv by multiple-stage linear ion-trap high-resolution mass spectrometry with electrospray ionization reveals that the family of sulfolipid II predominates. Rhoades ER; Streeter C; Turk J; Hsu FF Biochemistry; 2011 Oct; 50(42):9135-47. PubMed ID: 21919534 [TBL] [Abstract][Full Text] [Related]
29. A Screen for Protein-Protein Interactions in Live Mycobacteria Reveals a Functional Link between the Virulence-Associated Lipid Transporter LprG and the Mycolyltransferase Antigen 85A. Touchette MH; Van Vlack ER; Bai L; Kim J; Cognetta AB; Previti ML; Backus KM; Martin DW; Cravatt BF; Seeliger JC ACS Infect Dis; 2017 May; 3(5):336-348. PubMed ID: 28276676 [TBL] [Abstract][Full Text] [Related]
30. Two Accessory Proteins Govern MmpL3 Mycolic Acid Transport in Mycobacteria. Fay A; Czudnochowski N; Rock JM; Johnson JR; Krogan NJ; Rosenberg O; Glickman MS mBio; 2019 Jun; 10(3):. PubMed ID: 31239378 [TBL] [Abstract][Full Text] [Related]
31. Biochemical function of msl5 (pks8 plus pks17) in Mycobacterium tuberculosis H37Rv: biosynthesis of monomethyl branched unsaturated fatty acids. Dubey VS; Sirakova TD; Cynamon MH; Kolattukudy PE J Bacteriol; 2003 Aug; 185(15):4620-5. PubMed ID: 12867474 [TBL] [Abstract][Full Text] [Related]
32. Disruption of a gene essential for sulfoquinovosyldiacylglycerol biosynthesis in Sinorhizobium meliloti has no detectable effect on root nodule symbiosis. Weissenmayer B; Geiger O; Benning C Mol Plant Microbe Interact; 2000 Jun; 13(6):666-72. PubMed ID: 10830266 [TBL] [Abstract][Full Text] [Related]
34. Disruption of msl3 abolishes the synthesis of mycolipanoic and mycolipenic acids required for polyacyltrehalose synthesis in Mycobacterium tuberculosis H37Rv and causes cell aggregation. Dubey VS; Sirakova TD; Kolattukudy PE Mol Microbiol; 2002 Sep; 45(5):1451-9. PubMed ID: 12207710 [TBL] [Abstract][Full Text] [Related]
35. Attenuation of Mycobacterium tuberculosis by disruption of a mas-like gene or a chalcone synthase-like gene, which causes deficiency in dimycocerosyl phthiocerol synthesis. Sirakova TD; Dubey VS; Cynamon MH; Kolattukudy PE J Bacteriol; 2003 May; 185(10):2999-3008. PubMed ID: 12730158 [TBL] [Abstract][Full Text] [Related]
36. Rv2190c, an NlpC/P60 family protein, is required for full virulence of Mycobacterium tuberculosis. Parthasarathy G; Lun S; Guo H; Ammerman NC; Geiman DE; Bishai WR PLoS One; 2012; 7(8):e43429. PubMed ID: 22952680 [TBL] [Abstract][Full Text] [Related]
37. The three Mycobacterium tuberculosis antigen 85 isoforms have unique substrates and activities determined by non-active site regions. Backus KM; Dolan MA; Barry CS; Joe M; McPhie P; Boshoff HI; Lowary TL; Davis BG; Barry CE J Biol Chem; 2014 Sep; 289(36):25041-53. PubMed ID: 25028517 [TBL] [Abstract][Full Text] [Related]
38. Biosynthesis and Regulation of Sulfomenaquinone, a Metabolite Associated with Virulence in Mycobacterium tuberculosis. Sogi KM; Holsclaw CM; Fragiadakis GK; Nomura DK; Leary JA; Bertozzi CR ACS Infect Dis; 2016 Nov; 2(11):800-806. PubMed ID: 27933784 [TBL] [Abstract][Full Text] [Related]
39. A point mutation in the two-component regulator PhoP-PhoR accounts for the absence of polyketide-derived acyltrehaloses but not that of phthiocerol dimycocerosates in Mycobacterium tuberculosis H37Ra. Chesne-Seck ML; Barilone N; Boudou F; Gonzalo Asensio J; Kolattukudy PE; MartÃn C; Cole ST; Gicquel B; Gopaul DN; Jackson M J Bacteriol; 2008 Feb; 190(4):1329-34. PubMed ID: 18065542 [TBL] [Abstract][Full Text] [Related]