Zobrazeno 1 - 10
of 242
pro vyhledávání: '"Andrew G Myers"'
Autor:
Nozomu Obana, Hiraku Takada, Caillan Crowe-McAuliffe, Mizuki Iwamoto, Artyom A Egorov, Kelvin J Y Wu, Shinobu Chiba, Victoriia Murina, Helge Paternoga, Ben I C Tresco, Nobuhiko Nomura, Andrew G Myers, Gemma C Atkinson, Daniel N Wilson, Vasili Hauryliuk
Publikováno v:
Nucleic Acids Research. 51:4536-4554
Genome-encoded antibiotic resistance (ARE) ATP-binding cassette (ABC) proteins of the F subfamily (ARE-ABCFs) mediate intrinsic resistance in diverse Gram-positive bacteria. The diversity of chromosomally-encoded ARE-ABCFs is far from being fully exp
Publikováno v:
The Journal of Organic Chemistry.
Autor:
Nozomu Obana, Hiraku Takada, Caillan Crowe-McAuliffe, Mizuki Iwamoto, Artyom A. Egorov, Kelvin J.Y. Wu, Victoriia Murina, Helge Paternoga, Ben I.C. Tresco, Nobuhiko Nomura, Andrew G. Myers, Gemma C. Atkinson, Daniel N. Wilson, Vasili Hauryliuk
Genome-encoded antibiotic resistance (ARE) ATP-binding cassette (ABC) proteins of the F subfamily (ARE-ABCFs) mediate intrinsic resistance in diverse Gram-positive bacteria. The diversity of chromosomally-encoded ARE-ABCFs is far from being fully exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82cc36fda8320347a4d762cc19615334
https://doi.org/10.1101/2022.12.05.519065
https://doi.org/10.1101/2022.12.05.519065
Publikováno v:
Journal of the American Chemical Society. 143:11019-11025
A gram-scale synthesis of iboxamycin, an antibiotic candidate bearing a fused bicyclic amino acid residue, is presented. A pivotal transformation in the route involves an intramolecular hydrosilylation-oxidation sequence to set the ring-fusion stereo
Autor:
Andrew G. Myers, Roger B Clark
Publikováno v:
Accounts of Chemical Research. 54:1635-1645
Macrolides are among the most widely prescribed antibiotics, particularly for bacterial lung infections, due to their favorable safety, oral bioavailability, and spectrum of activity against Gram-positive pathogens such as Streptococcus pneumoniae, t
Autor:
Mark P. Jedrychowski, Pedro Latorre-Muro, Christopher F. Bennett, Kamar Reda, Steven P. Gygi, Elizabeth A. Perry, Richard Porter Ladley, Katherine E. O’Malley, Chi Luo, Eduardo Balsa, Andrew G. Myers, Peter M. Wright, Pere Puigserver
Publikováno v:
Nature metabolism
Mitochondrial diseases (MDs) are a heterogeneous group of disorders resulting from mutations in nuclear or mitochondrial DNA genes encoding mitochondrial proteins1,2. MDs cause pathologies with severe tissue damage and ultimately death3,4. There are
Autor:
Hiraku, Takada, Zachary F, Mandell, Helen, Yakhnin, Anastasiya, Glazyrina, Shinobu, Chiba, Tatsuaki, Kurata, Kelvin J Y, Wu, Ben I C, Tresco, Andrew G, Myers, Gemma C, Aktinson, Paul, Babitzke, Vasili, Hauryliuk
Publikováno v:
Nucleic acids research. 50(11)
Since antibiotic resistance is often associated with a fitness cost, bacteria employ multi-layered regulatory mechanisms to ensure that expression of resistance factors is restricted to times of antibiotic challenge. In Bacillus subtilis, the chromos
Autor:
Tetiana, Brodiazhenko, Kathryn Jane, Turnbull, Kelvin J Y, Wu, Hiraku, Takada, Ben I C, Tresco, Tanel, Tenson, Andrew G, Myers, Vasili, Hauryliuk
Publikováno v:
JAC-antimicrobial resistance. 4(3)
Listeriosis is a food-borne disease caused by the Gram-positive Bacillota (Firmicute) bacteriumWe have established newly developed lincosamide iboxamycin as a potential novel antilisterial agent.We determined MICs of the lincosamides lincomycin, clin
Autor:
Tetiana Brodiazhenko, Kathryn Jane Turnbull, Kelvin J.Y. Wu, Hiraku Takada, Ben I.C. Tresco, Tanel Tenson, Andrew G. Myers, Vasili Hauryliuk
Listeriosis is a dangerous food-borne bacterial disease caused by the Gram-positive Bacillota (Firmicute) bacterium Listeria monocytogenes. In this report, we show that the synthetic lincosamide iboxamycin is highly active against L. monocytogenes an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8e024d1ea69c1c277e792ec2e7e9696
https://doi.org/10.1101/2022.02.28.482263
https://doi.org/10.1101/2022.02.28.482263
Publikováno v:
Journal of the American Chemical Society. 143(18)
The development of a flexible, component-based synthetic route to the aminosugar fragment of the lincosamide antibiotics is described. This synthetic route hinges on the application and extension of nitroaldol chemistry to forge strategic bonds withi