Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Daniel S. Catlin"'
Autor:
Richard B. Silverman, Peter F. Doubleday, Neil L. Kelleher, Timothy A Dwight, Arseniy Butrin, Daniel S. Catlin, Pathum M. Weerawarna, Dali Liu, Rafael D. Melani, Wei Zhu
Publikováno v:
Journal of the American Chemical Society. 143:8193-8207
Human ornithine aminotransferase (hOAT) is a pyridoxal 5'-phosphate (PLP)-dependent enzyme that was recently found to play an important role in the metabolic reprogramming of hepatocellular carcinoma (HCC) via the proline and glutamine metabolic path
Autor:
Peter F. Doubleday, Neil L. Kelleher, Daniel S. Catlin, Richard B. Silverman, Dali Liu, Matthew J. Moschitto
Publikováno v:
Journal of the American Chemical Society. 141:10711-10721
The inhibition of ornithine aminotransferase (OAT), a pyridoxal 5'-phosphate-dependent enzyme, has been implicated as a treatment for hepatocellular carcinoma (HCC), the most common form of liver cancer, for which there is no effective treatment. Fro
Autor:
Wei, Zhu, Peter F, Doubleday, Arseniy, Butrin, Pathum M, Weerawarna, Rafael D, Melani, Daniel S, Catlin, Timothy A, Dwight, Dali, Liu, Neil L, Kelleher, Richard B, Silverman
Publikováno v:
J Am Chem Soc
Human ornithine aminotransferase (hOAT) is a pyridoxal 5′-phosphate (PLP)-dependent enzyme that was recently found to play an important role in the metabolic reprogramming of hepatocellular carcinoma (HCC) via proline and glutamine metabolic pathwa
Autor:
Rachel M. Bleich, Jonathan W. Bogart, Aneta Turlik, R. Thomas Williamson, Daniel S. Catlin, Albert A. Bowers, Frank C. Schroeder, Nicholas J. Kramer, Satish K. Nair, K. N. Houk
Publikováno v:
J Am Chem Soc
Thiopeptides are a broad class of macrocyclic, heavily modified peptide natural products that are unified by the presence of a substituted, nitrogen-containing heterocycle core. Early work indicated that this core might be fashioned from two dehydroa
Autor:
Daniel S. Catlin, Thomas R. Trzupek, Daniel P. Becker, Brian L Cannon, Cory T. Reidl, Richard B. Silverman, Dali Liu
Publikováno v:
Protein Sci
Addressing molecular recognition in the context of evolution requires pursuing new molecular targets to enable the development of agonists or antagonists with new mechanisms of action. Disruption of transcriptional regulation through targeting transc
Publikováno v:
J Biol Chem
Cleavage of aromatic carbon–chlorine bonds is critical for the degradation of toxic industrial compounds. Here, we solved the X-ray crystal structure of chlorothalonil dehalogenase (Chd) from Pseudomonas sp. CTN-3, with 15 of its N-terminal residue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c7baec14ea6e2123c03b30732ec94ef
https://europepmc.org/articles/PMC7324493/
https://europepmc.org/articles/PMC7324493/
Autor:
Matthew J, Moschitto, Peter F, Doubleday, Daniel S, Catlin, Neil L, Kelleher, Dali, Liu, Richard B, Silverman
Publikováno v:
J Am Chem Soc
The inhibition of ornithine aminotransferase (OAT), a pyridoxal 5′-phosphate-dependent enzyme, has been implicated as a treatment for hepatocellular carcinoma (HCC), the most common form of liver cancer, for which there is no effective treatment. F
Autor:
Neil L. Kelleher, Rui Wu, Eric J. Drake, Walter Fast, Dali Liu, Andrew M. Gulick, Kenneth D. Clevenger, Romila Mascarenhas, Daniel S. Catlin
Publikováno v:
ACS chemical biology. 12(3)
Siderophore biosynthesis by Pseudomonas aeruginosa enhances virulence and represents an attractive drug target. PvdQ functions in the type-1 pyoverdine biosynthetic pathway by removing a myristoyl anchor from a pyoverdine precursor, allowing eventual