Deborah L. Zink spends much of her time researching Stereochemistry, Biochemistry, Enzyme, Natural product and Biological activity. Her Stereochemistry research includes elements of Integrase, Platensimycin, Organic chemistry and Enzyme inhibitor. In her research, she performs multidisciplinary study on Biochemistry and Apicidin.
Her Enzyme research is multidisciplinary, incorporating elements of IC50, Antibacterial agent, Bacterial growth and Phoma. Deborah L. Zink has included themes like Streptomyces, Chemical synthesis, Acyl carrier protein synthase and Cyclohexenone in her Antibacterial agent study. Her Natural product research incorporates themes from Antibacterial activity, Antibiotic resistance, Staphylococcus aureus and DNA gyrase.
Her primary areas of study are Stereochemistry, Biochemistry, Biological activity, Enzyme and Microbiology. Her studies in Stereochemistry integrate themes in fields like Platensimycin and Antifungal. Her Biochemistry research is multidisciplinary, incorporating perspectives in Isolation and Antibacterial activity.
The concepts of her Antibacterial activity study are interwoven with issues in Antibacterial agent and Peptide. Deborah L. Zink works mostly in the field of Enzyme, limiting it down to concerns involving Integrase and, occasionally, Inhibitory postsynaptic potential and Recombinant DNA. In her work, Ribosomal RNA is strongly intertwined with Staphylococcus aureus, which is a subfield of Microbiology.
Her primary scientific interests are in Biochemistry, Microbiology, Antibacterial activity, Stereochemistry and Antibiotics. Deborah L. Zink studies Enzyme which is a part of Biochemistry. As a part of the same scientific study, she usually deals with the Microbiology, concentrating on Biological activity and frequently concerns with Peptide.
In her study, which falls under the umbrella issue of Antibacterial activity, Protein biosynthesis is strongly linked to Antibacterial agent. Her studies deal with areas such as Platensimycin and Polyketide as well as Stereochemistry. In her research, Neosartorya glabra and Neosartorya is intimately related to Staphylococcus aureus, which falls under the overarching field of Antibiotics.
Deborah L. Zink mainly focuses on Biochemistry, Microbiology, Antibacterial activity, Antibiotics and Isolation. Her Biochemistry study integrates concerns from other disciplines, such as Trichophyton and Streptomycetaceae, Actinomycetales. Her research in Antibacterial activity intersects with topics in Platensimycin, Antibacterial agent, Peptide and Stereochemistry.
She interconnects Biosynthesis and Enzyme in the investigation of issues within Stereochemistry. Her Antibiotics study combines topics from a wide range of disciplines, such as Neosartorya glabra and Staphylococcus aureus. Her work in Biological activity addresses subjects such as Candida albicans, which are connected to disciplines such as Genome and Fermentation.
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Isolation, structure, and absolute stereochemistry of platensimycin, a broad spectrum antibiotic discovered using an antisense differential sensitivity strategy.
Sheo B. Singh;Hiranthi Jayasuriya;John G. Ondeyka;Kithsiri B. Herath.
Journal of the American Chemical Society (2006)
Isolation and Structure of Platencin: A FabH and FabF Dual Inhibitor with Potent Broad‐Spectrum Antibiotic Activity
Hiranthi Jayasuriya;Kithsiri B. Herath;Chaowei Zhang;Deborah L. Zink.
Angewandte Chemie (2007)
Equisetin and a novel opposite stereochemical homolog phomasetin, two fungal metabolites as inhibitors of HIV-1 integrase
Sheo B. Singh;Deborah L. Zink;Michael A. Goetz;Anne W. Dombrowski.
Tetrahedron Letters (1998)
Nodulisporic Acid A, a Novel and Potent Insecticide from a Nodulisporium Sp. Isolation, Structure Determination, and Chemical Transformations
John G. Ondeyka;Gregory L. Helms;Otto D. Hensens;Michael A. Goetz.
Journal of the American Chemical Society (1997)
Apicidins: Novel cyclic tetrapeptides as coccidiostats and antimalarial agents from Fusarium pallidoroseum
Sheo B. Singh;Deborah L. Zink;Jon D. Polishook;Anne W. Dombrowski.
Tetrahedron Letters (1996)
Structure and Chemistry of Apicidins, a Class of Novel Cyclic Tetrapeptides without a Terminal α-Keto Epoxide as Inhibitors of Histone Deacetylase with Potent Antiprotozoal Activities
Sheo B. Singh;Deborah L. Zink;Jerrold M. Liesch;Ralph T. Mosley.
Journal of Organic Chemistry (2002)
Discovery of Kibdelomycin, A Potent New Class of Bacterial Type II Topoisomerase Inhibitor by Chemical-Genetic Profiling in Staphylococcus aureus
John W. Phillips;Michael A. Goetz;Scott K. Smith;Deborah L. Zink.
Chemistry & Biology (2011)
Resorcylic Acid Lactones: Naturally Occurring Potent and Selective Inhibitors of MEK
Annie Zhao;Seok H. Lee;Seok H. Lee;Marina Moiena;Rosalind G. Jenkins.
The Journal of Antibiotics (1999)
Isolation and structure of chaetomellic acids A and B from Chaetomella acutiseta: farnesyl pyrophosphate mimic inhibitors of ras farnesyl-protein transferase
Sheo B. Singh;Deborah L. Zink;Jerrold M. Liesch;Michael A. Goetz.
Tetrahedron (1993)
Isolation, structure, and HIV-1-integrase inhibitory activity of structurally diverse fungal metabolites
Sheo B. Singh;Hiranthi Jayasuriya;Raymond Dewey;Jon D. Polishook.
Journal of Industrial Microbiology & Biotechnology (2003)
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