Nitesh V. Sule, Ph.D.
Affiliations: | 2013 | Chemistry and Biochemistry | North Dakota State University, Fargo, ND, United States |
Area:
Biochemistry, General BiophysicsGoogle:
"Nitesh Sule"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| DK Srivastava | grad student | 2013 | North Dakota State University | |
| (Mechanistic studies on the methionine aminopeptidase and peptide deformylase catalyzed reactions.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Pasupuleti S, Sule N, Manson MD, et al. (2017) Conversion of Norepinephrine to 3,4-Dihdroxymandelic Acid in Escherichia coli Requires the QseBC Quorum-Sensing System and the FeaR Transcription Factor. Journal of Bacteriology |
| Sule NV, Ugrinov A, Mallik S, et al. (2015) Bridging of a substrate between cyclodextrin and an enzyme's active site pocket triggers a unique mode of inhibition. Biochimica Et Biophysica Acta. 1850: 141-9 |
| Pasupuleti S, Sule N, Cohn WB, et al. (2014) Chemotaxis of Escherichia coli to norepinephrine (NE) requires conversion of NE to 3,4-dihydroxymandelic acid. Journal of Bacteriology. 196: 3992-4000 |
| Sule N, Singh RK, Zhao P, et al. (2012) Probing the metal ion selectivity in methionine aminopeptidase via changes in the luminescence properties of the enzyme bound europium ion. Journal of Inorganic Biochemistry. 106: 84-9 |
| Singh RK, Mandal T, Balsubramanian N, et al. (2011) Histone deacetylase activators: N-acetylthioureas serve as highly potent and isozyme selective activators for human histone deacetylase-8 on a fluorescent substrate. Bioorganic & Medicinal Chemistry Letters. 21: 5920-3 |
| Sule N, Singh R, Srivastava DK. (2008) Alternative Modes of Binding of Recombinant Human Histone Deacetylase 8 to Colloidal Gold Nanoparticles. Journal of Biomedical Nanotechnology. 4: 463-468 |
| Haldar MK, Scott MD, Sule N, et al. (2008) Synthesis of barbiturate-based methionine aminopeptidase-1 inhibitors. Bioorganic & Medicinal Chemistry Letters. 18: 2373-6 |