Mol Cell Biochem 1994, 140:1–22 PubMedCrossRef 46 Cesnek M, Hock

Mol Cell Biochem 1994, 140:1–22.PubMedCrossRef 46. Cesnek M, Hockova D, Holy A, Dracinsky M, Baszczynski O, Jersey J, DT K, Guddat L: Synthesis of 9-phosphonoalkyl and 9-phosphonoalkoxyalkyl purines: evaluation of their ability to act as inhibitors of Plasmodium falciparum , Plasmodium vivax and human hypoxanthine-guanine-(xanthine) phosphoribosyltransferases. Bioorg Med Chem 2012, 20:1076–1089.PubMedCrossRef 47. Sun X, Sharling L, Muthalagi M, Mudeppa D, Pankiewicz K, Felczak K, Rathod P, Mead J, Striepen B, Hedstrom L: Prodrug activation by Cryptosporidium thymidine kinase. J Biol Chem 2010, 285:15916–15922.PubMedCrossRef 48. Sandrini M, Shannon O, Clausen A, Björck L, Piskur J: Deoxyribonucleoside

kinases activate nucleoside antibiotics in severely pathogenic bacteria. Antimicrob Agents Chemother 2007, 51:2726–2732.PubMedCrossRef 49. Halbedel S, Stülke ARN-509 datasheet J: Dual phosphorylation of Mycoplasma pneumoniae HPr by enzyme I and HPr kinase suggests an extended phosphoryl group susceptibility of HPr. FEMS Microbiol Lett 2004, 247:193–198.CrossRef find more 50. Okazaki N, Narita M, Yamada S, Izumikawa K, Umetsu M, Kenri Y, Sasaky Y, Arakawa Y, Sasaky T: Characteristics of macrolide-resistant Mycoplasma pneumoniae strains isolated from patients and induced with erythromycin in vitro. Microbiol Immunol 2001, 45:617–620.PubMed 51. Sharif H, von Euler H, Westberg S, He E,

Wang L, Eriksson S: A sensitive and kinetically defined radiochemical assay for canine and human serum thymidine kinase 1 (TK1) to monitor canine malignant lymphoma. Vet J 2012, 194:40–47.PubMedCrossRef 52. Wang L: The role of Ureaplasma nucleoside monophosphate kinases in the synthesis of nucleoside triphosphates. FEBS J 2007, 274:1983–1990.PubMedCrossRef

Competing interests Resveratrol Both authors declare that they have no competing interests. Authors’ contributions RS performed the kinetic and inhibitions studies with thymidine kinases, analyzed the data and created the figures; LW designed the study, performed growth inhibition studies, uptake and metabolism of labelled nucleosides, characterized Mpn HPRT; analyzed the data and wrote the manuscript. All authors have read and approved the manuscript.”
“Correction After the publication of this work [1], we became aware that the legends for Figures 2, 3 and 4 were not in the correct order. The legends should be as BV-6 research buy follows: Figure 2: Escherichia coli lambda lysogen DNA and average transcript levels after treatment with 10 J/m2 UV light. The x-axis is the position of genes on the E. coli chromosome. The E. coli origin is at the 0 position on the x-axis. The lambda integration site attB is indicated by the vertical line. The y-axis is the log ratio of treated to untreated cells. A). Average transcription (100 bins) along the E. coli chromosome at 20, 40, 60 minutes after exposure to UV light. B). Ratio of DNA 60 minutes after treatment with UV light relative to DNA of untreated cells.

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