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A community resource for paired genomic and metabolomic data mining
A community resource for paired genomic and metabolomic data mining
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A community resource for paired genomic and metabolomic data mining

Michelle A. Schorn Stefan Verhoeven; Lars Ridder; Florian Huber; Deepa D. A Acharya; Alexander A Aksenov; Gajender Aleti; Jamshid Amiri Moghaddam; Allegra T Aron; Saefuddin Aziz; Anelize Bauermeister; Katherine D Bauman; Martin Baunach; Christine Beemelmanns; J. Michael Beman; María Victoria Berlanga Clavero; Alex A Blacutt; Helge B Bode; Anne Boullie; Asker Brejnrod; Tim S Bugni; Alexandra Calteau; Liu Cao; Víctor J Carrión; Raquel Castelo Branco; Shaurya Chanana; Alexander B Chase; Marc G Chevrette; Letícia Veras Costa-Lotufo; Jason M Crawford; Cameron R Currie; Bart Cuypers; Tam Dang; Tristan de Rond; Alyssa M Demko; Elke Dittmann; Chao Du; Christopher Drozd; Jean-Claude Dujardin; Rachel J Dutton; Ann Edlund; David P Fewer; Neha Garg; Julia M Gauglitz; Emily C Gentry; Lena Gerwick; Evgenia Glukhov; Harald Gross; Muriel Gugger; Dulce G. Guillén Matus; Eric J. N Helfrich; Benjamin-Florian Hempel; Jae-Seoun Hur; Marianna Iorio; Paul R Jensen; Kyo Bin Kang; Leonard Kaysser; Neil L Kelleher; Chung Sub Kim; Ki Hyun Kim; Irina Koester; Gabriele M König; Tiago Leao; Seoung Rak Lee; Yi-Yuan Lee; Xuanji Li; Jessica C Little Maloney,Katherine N.; Daniel Männle; Christian Martin H.; Andrew C McAvoy; Willam W Metcalf; Hosein Mohimani; Carlos Molina Santiago; Bradley S Moore; Michael W Mullowney; Mitchell Muskat; Louis Félix Nothias; Ellis C O’Neill; Elizabeth I Parkinson; Daniel Petras; Jörn Piel; Emily C Pierce; Karine Pires; Raphael Reher; Diego Romero; M. Caroline Roper; Michael Rust; Hamada Saad; Carmen Saenz; Laura M Sanchez; Søren Johann Sørensen; Margherita Sosio; Roderich D Süssmuth; Douglas Sweeney; Kapil Tahlan; Regan J Thomson; Nicholas J Tobias; Amaro Emiliano Trindade Silva; Gilles P. van Wezel; Mingxun Wang; Kelly C Weldon; Fan Zhang; Nadine Ziemert; Katherine R Duncan; Max Crüsemann; Simon Rogers; Pieter C Dorrestein; Marnix H Medema; Justin J. J. van der Hooft

Nature Chemical Biology London 8 p., 2021

London 2021

Item não circula. Consulte sua biblioteca.(Acessar)

2
Bioactive Peptide Natural Products as Lead Structures for Medicinal Use
Bioactive Peptide Natural Products as Lead Structures for Medicinal Use
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Bioactive Peptide Natural Products as Lead Structures for Medicinal Use

Dang, Tam ; Süssmuth, Roderich D

Accounts of chemical research, 2017-07, Vol.50 (7), p.1566-1576 [Periódico revisado por pares]

United States: American Chemical Society

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3
Self-Assembled Monolayer Epitope Bridges for Molecular Imprinting and Cancer Biomarker Sensing
Self-Assembled Monolayer Epitope Bridges for Molecular Imprinting and Cancer Biomarker Sensing
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Self-Assembled Monolayer Epitope Bridges for Molecular Imprinting and Cancer Biomarker Sensing

Drzazgowska, Julia ; Schmid, Bianca ; Süssmuth, Roderich D ; Altintas, Zeynep

Analytical chemistry (Washington), 2020-04, Vol.92 (7), p.4798-4806 [Periódico revisado por pares]

United States: American Chemical Society

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4
Venom Proteomics of Indonesian King Cobra, Ophiophagus hannah: Integrating Top-Down and Bottom-Up Approaches
Venom Proteomics of Indonesian King Cobra, Ophiophagus hannah: Integrating Top-Down and Bottom-Up Approaches
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Venom Proteomics of Indonesian King Cobra, Ophiophagus hannah: Integrating Top-Down and Bottom-Up Approaches

Petras, Daniel ; Heiss, Paul ; Süssmuth, Roderich D. ; Calvete, Juan J.

Journal of proteome research, 2015-06, Vol.14 (6), p.2539-2556 [Periódico revisado por pares]

United States: American Chemical Society

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5
A Self‐Sacrificing N‐Methyltransferase Is the Precursor of the Fungal Natural Product Omphalotin
A Self‐Sacrificing N‐Methyltransferase Is the Precursor of the Fungal Natural Product Omphalotin
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A Self‐Sacrificing N‐Methyltransferase Is the Precursor of the Fungal Natural Product Omphalotin

Ramm, Sascha ; Krawczyk, Bartlomiej ; Mühlenweg, Agnes ; Poch, Annette ; Mösker, Eva ; Süssmuth, Roderich D.

Angewandte Chemie International Edition, 2017-08, Vol.56 (33), p.9994-9997 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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6
Biochemical Dissection of the Natural Diversification of Microcystin Provides Lessons for Synthetic Biology of NRPS
Biochemical Dissection of the Natural Diversification of Microcystin Provides Lessons for Synthetic Biology of NRPS
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Biochemical Dissection of the Natural Diversification of Microcystin Provides Lessons for Synthetic Biology of NRPS

Meyer, Sabine ; Kehr, Jan-Christoph ; Mainz, Andi ; Dehm, Daniel ; Petras, Daniel ; Süssmuth, Roderich D. ; Dittmann, Elke

Cell chemical biology, 2016-04, Vol.23 (4), p.462-471 [Periódico revisado por pares]

United States: Elsevier Ltd

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7
Iodine-Mediated Tryptathionine Formation Facilitates the Synthesis of Amanitins
Iodine-Mediated Tryptathionine Formation Facilitates the Synthesis of Amanitins
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Iodine-Mediated Tryptathionine Formation Facilitates the Synthesis of Amanitins

Yao, Guiyang ; Knittel, Caroline H ; Kosol, Simone ; Wenz, Marius T ; Keller, Bettina G ; Gruß, Hendrik ; Braun, Alexandra C ; Lutz, Christian ; Hechler, Torsten ; Pahl, Andreas ; Süssmuth, Roderich D

Journal of the American Chemical Society, 2021-09, Vol.143 (35), p.14322-14331 [Periódico revisado por pares]

United States: American Chemical Society

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8
Plantazolicin, a Novel Microcin B17/Streptolysin S-Like Natural Product from Bacillus amyloliquefaciens FZB42
Plantazolicin, a Novel Microcin B17/Streptolysin S-Like Natural Product from Bacillus amyloliquefaciens FZB42
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Plantazolicin, a Novel Microcin B17/Streptolysin S-Like Natural Product from Bacillus amyloliquefaciens FZB42

SCHOLZ, Romy ; MOLOHON, Katie J ; NACHTIGALL, Jonny ; VATER, Joachim ; MARKLEY, Andrew L ; SÜSSMUTH, Roderich D ; MITCHELL, Douglas A ; BORRISS, Rainer

Journal of Bacteriology, 2011-01, Vol.193 (1), p.215-224 [Periódico revisado por pares]

Washington, DC: American Society for Microbiology

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9
The anti-staphylococcal lipolanthines are ribosomally synthesized lipopeptides
The anti-staphylococcal lipolanthines are ribosomally synthesized lipopeptides
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The anti-staphylococcal lipolanthines are ribosomally synthesized lipopeptides

Wiebach, Vincent ; Mainz, Andi ; Siegert, Mary-Ann J ; Jungmann, Natalia A ; Lesquame, Guillaume ; Tirat, Sophie ; Dreux-Zigha, Assia ; Aszodi, Jozsef ; Le Beller, Dominique ; Süssmuth, Roderich D

Nature chemical biology, 2018-07, Vol.14 (7), p.652-654 [Periódico revisado por pares]

United States: Nature Publishing Group

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10
The lantibiotic peptide labyrinthopeptin A1 demonstrates broad anti-HIV and anti-HSV activity with potential for microbicidal applications
The lantibiotic peptide labyrinthopeptin A1 demonstrates broad anti-HIV and anti-HSV activity with potential for microbicidal applications
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The lantibiotic peptide labyrinthopeptin A1 demonstrates broad anti-HIV and anti-HSV activity with potential for microbicidal applications

Férir, Geoffrey ; Petrova, Mariya I ; Andrei, Graciela ; Huskens, Dana ; Hoorelbeke, Bart ; Snoeck, Robert ; Vanderleyden, Jos ; Balzarini, Jan ; Bartoschek, Stefan ; Brönstrup, Mark ; Süssmuth, Roderich D ; Schols, Dominique Favoreel, Herman

PloS one, 2013-05, Vol.8 (5), p.e64010-e64010 [Periódico revisado por pares]

United States: Public Library of Science

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Deste Autor:

  1. Kang, K
  2. Dittmann, E
  3. Hempel, B
  4. Verhoeven, S
  5. McAvoy, A

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