| Year |
Citation |
Score |
| 2012 |
Viswanathan K, Frey KM, Scocchera EW, Martin BD, Swain Iii PW, Alverson JB, Priestley ND, Anderson AC, Wright DL. Toward new therapeutics for skin and soft tissue infections: propargyl-linked antifolates are potent inhibitors of MRSA and Streptococcus pyogenes. Plos One. 7: e29434. PMID 22347365 DOI: 10.1371/Journal.Pone.0029434 |
0.226 |
|
| 2011 |
Sumskaya YG, Swain PW, Bergmeier SC, McMills MC, Priestley ND, Wrighta DL. Natural feedstocks for diversity-oriented synthesis: Macrolide-like scaffolds from nonactate Arkivoc. 2011: 144-166. DOI: 10.3998/Ark.5550190.0012.513 |
0.313 |
|
| 2010 |
Phillips JB, Smith AE, Kusche BR, Bessette BA, Swain PW, Bergmeier SC, McMills MC, Wright DL, Priestley ND. Natural product derivatives with bactericidal activity against Gram-positive pathogens including methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecalis. Bioorganic & Medicinal Chemistry Letters. 20: 5936-8. PMID 20801034 DOI: 10.1016/J.Bmcl.2010.06.146 |
0.272 |
|
| 2006 |
Dinges JM, Bessette BA, Cox JE, Redder CR, Priestley ND. Lipase-mediated purification of methyl nonactate, an important natural product building block for diversity-oriented synthesis. Biotechnology Progress. 22: 1354-7. PMID 17022674 DOI: 10.1021/bp0601138 |
0.321 |
|
| 2006 |
Nikodinovic J, Dinges JM, Bergmeier SC, McMills MC, Wright DL, Priestley ND. Resolution of methyl nonactate by Rhodococcus erythropolis under aerobic and anaerobic conditions. Organic Letters. 8: 443-5. PMID 16435855 DOI: 10.1021/Ol052739P |
0.286 |
|
| 1999 |
Walczak RJ, Dickens ML, Priestley ND, Strohl WR. Purification, properties, and characterization of recombinant Streptomyces sp. strain C5 DoxA, a cytochrome P-450 catalyzing multiple steps in doxorubicin biosynthesis. Journal of Bacteriology. 181: 298-304. PMID 9864343 DOI: 10.1128/Jb.181.1.298-304.1999 |
0.316 |
|
| 1997 |
Valentine AM, Wilkinson B, Liu KE, Komar-Panicucci S, Priestley ND, Williams PG, Morimoto H, Floss HG, Lippard SJ. Tritiated chiral alkanes as substrates for soluble methane monooxygenase from Methylococcus capsulatus (Bath): Probes for the mechanism of hydroxylation Journal of the American Chemical Society. 119: 1818-1827. DOI: 10.1021/Ja963971G |
0.516 |
|
| 1996 |
Priestley ND, Smith TM, Shipley PR, Floss HG. Studies on the biosynthesis of thiostrepton: 4-(1-hydroxyethyl)quinoline-2-carboxylate as a free intermediate on the pathway to the quinaldic acid moiety. Bioorganic & Medicinal Chemistry. 4: 1135-47. PMID 8831986 DOI: 10.1016/0968-0896(96)00126-5 |
0.573 |
|
| 1996 |
Wilkinson B, Zhu M, Priestley ND, Nguyen HHT, Morimoto H, Williams PG, Chan SI, Floss HG. A concerted mechanism for ethane hydroxylation by the particulate methane monooxygenase from Methylococcus capsulatus (bath) Journal of the American Chemical Society. 118: 921-922. DOI: 10.1021/Ja953407Q |
0.515 |
|
| 1993 |
Smith TM, Priestley ND, Knaggs AR, Nguyen T, Floss HG. 3,4-Dimethylindole-2-carboxylate and 4-(1-hydroxyethyl)quinoline-2-carboxylate activating enzymes from the nosiheptide and thiostrepton producers, Streptomyces actuosus and Streptomyces laurentii Journal of the Chemical Society - Series Chemical Communications. 1612-1614. DOI: 10.1039/C39930001612 |
0.559 |
|
| 1993 |
Froland WA, Priestley ND, Floss HG, Williams PG, Morimoto H, Lipscomb JD. Evidence supporting the formation of a substrate radical during H2O2-coupled MMO catalyzed oxidation of chiral ethane Journal of Inorganic Biochemistry. 51: 245. DOI: 10.1016/0162-0134(93)85279-H |
0.525 |
|
| 1992 |
Priestley ND, Floss HG, Froland WA, Lipscomb JD, Williams PG, Morimoto H. Cryptic stereospecificity of methane monooxygenase Journal of the American Chemical Society. 114: 7561-7562. DOI: 10.1021/Ja00045A037 |
0.551 |
|
| 1989 |
Priestley ND, Robinson JA. Purification and catalytic properties of L-valine dehydrogenase from Streptomyces cinnamonensis. The Biochemical Journal. 261: 853-61. PMID 2803248 DOI: 10.1042/bj2610853 |
0.553 |
|
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