Thomas K. Hemscheidt

Affiliations: 
University of Hawai'i at Manoa, Honolulu, HI 
Area:
Organic Chemistry, Molecular Biology, Biochemistry
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"Thomas Hemscheidt"
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Publications

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Arnison PG, Bibb MJ, Bierbaum G, et al. (2013) Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature. Natural Product Reports. 30: 108-60
Christiansen G, Philmus B, Hemscheidt T, et al. (2011) Genetic variation of adenylation domains of the anabaenopeptin synthesis operon and evolution of substrate promiscuity. Journal of Bacteriology. 193: 3822-31
Fehér D, Barlow R, McAtee J, et al. (2010) Highly brominated antimicrobial metabolites from a marine Pseudoalteromonas sp. Journal of Natural Products. 73: 1963-6
Philmus B, Guerrette JP, Hemscheidt TK. (2009) Substrate specificity and scope of MvdD, a GRASP-like ligase from the microviridin biosynthetic gene cluster. Acs Chemical Biology. 4: 429-34
Schupp PJ, Kohlert-Schupp C, Yoshida WY, et al. (2009) Structure of pseudocerosine, an indolic azafulvene alkaloid from the flatworm Pseudoceros indicus. Organic Letters. 11: 1111-4
Okumura HS, Philmus B, Portmann C, et al. (2009) Homotyrosine-containing cyanopeptolins 880 and 960 and anabaenopeptins 908 and 915 from Planktothrix agardhii CYA 126/8. Journal of Natural Products. 72: 172-6
Philmus B, Christiansen G, Yoshida WY, et al. (2008) Post-translational modification in microviridin biosynthesis. Chembiochem : a European Journal of Chemical Biology. 9: 3066-73
Christiansen G, Yoshida WY, Blom JF, et al. (2008) Isolation and structure determination of two microcystins and sequence comparison of the McyABC adenylation domains in Planktothrix species. Journal of Natural Products. 71: 1881-6
Fehér D, Barlow RS, Lorenzo PS, et al. (2008) A 2-substituted prodiginine, 2-(p-hydroxybenzyl)prodigiosin, from Pseudoalteromonas rubra. Journal of Natural Products. 71: 1970-2
Ishida K, Christiansen G, Yoshida WY, et al. (2007) Biosynthesis and structure of aeruginoside 126A and 126B, cyanobacterial peptide glycosides bearing a 2-carboxy-6-hydroxyoctahydroindole moiety. Chemistry & Biology. 14: 565-76
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