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7 in total

Review 1. Natural products from thioester reductase containing biosynthetic pathways.

Authors: Michael W Mullowney; Ryan A McClure; Matthew T Robey; Neil L Kelleher; Regan J Thomson
Journal: Nat Prod Rep Date: 2018-09-19 Impact factor: 13.423

2. The cyclic octapeptide antibiotic argyrin B inhibits translation by trapping EF-G on the ribosome during translocation.

Authors: Maximiliane Wieland; Mikael Holm; Emily J Rundlet; Martino Morici; Timm O Koller; Tinashe P Maviza; Domen Pogorevc; Ilya A Osterman; Rolf Müller; Scott C Blanchard; Daniel N Wilson
Journal: Proc Natl Acad Sci U S A Date: 2022-05-02 Impact factor: 12.779

Review 3. The proteasome of malaria parasites: A multi-stage drug target for chemotherapeutic intervention?

Authors: Makoah Nigel Aminake; Hans-Dieter Arndt; Gabriele Pradel
Journal: Int J Parasitol Drugs Drug Resist Date: 2012-01-09 Impact factor: 4.077

4. Identification of elongation factor G as the conserved cellular target of argyrin B.

Authors: Beat Nyfeler; Dominic Hoepfner; Deborah Palestrant; Christina A Kirby; Lewis Whitehead; Robert Yu; Gejing Deng; Ruth E Caughlan; Angela L Woods; Adriana K Jones; S Whitney Barnes; John R Walker; Swann Gaulis; Ervan Hauy; Saskia M Brachmann; Philipp Krastel; Christian Studer; Ralph Riedl; David Estoppey; Thomas Aust; N Rao Movva; Zuncai Wang; Michael Salcius; Gregory A Michaud; Gregory McAllister; Leon O Murphy; John A Tallarico; Christopher J Wilson; Charles R Dean
Journal: PLoS One Date: 2012-09-10 Impact factor: 3.240

Elucidation of the structure and intermolecular interactions of a reversible cyclic-peptide inhibitor of the proteasome by NMR spectroscopy and molecular modeling.

Review 1. Natural products from thioester reductase containing biosynthetic pathways.

2. The cyclic octapeptide antibiotic argyrin B inhibits translation by trapping EF-G on the ribosome during translocation.

Review 3. The proteasome of malaria parasites: A multi-stage drug target for chemotherapeutic intervention?

4. Identification of elongation factor G as the conserved cellular target of argyrin B.

Review 5. Cyclic peptides as therapeutic agents and biochemical tools.

6. Natural product scaffolds as inspiration for the design and synthesis of 20S human proteasome inhibitors.

7. Biotechnological production optimization of argyrins - a potent immunomodulatory natural product class.