Stuart S. Licht, PhD
Affiliations: | 2002-2008 | Massachusetts Institute of Technology, Cambridge, MA, United States | |
2008-2010 | Novartis, Basel, Basel-Stadt, France | ||
2010- | sanofi-aventis, St. Louis, MO, United States |
Website:
https://www.linkedin.com/pub/stuart-licht/7/57a/610Google:
"Stuart Spencer Licht"Bio:
Licht, Stuart S. A kinetically competent thiyl radical intermediate in ribonucleotide reduction , thesis MIT (1998)
Mean distance: 15.69 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentorJoAnne Stubbe | grad student | 1998 | MIT (Chemistry Tree) | |
(A kinetically competent thiyl radical intermediate in ribonucleotide reduction) | ||||
Peter G. Schultz | post-doc | 2000-2001 | Scripps Research Institute (Chemistry Tree) | |
Anthony Auerbach | post-doc | 2001-2002 | SUNY Buffalo |
Children
Sign in to add traineeAmy Weeks | research assistant | MIT (Chemistry Tree) | |
Mathew C. Tantama | grad student | 2008 | MIT |
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. |
Deng G, Shen J, Yin M, et al. (2015) Selective inhibition of mutant isocitrate dehydrogenase 1 (IDH1) via disruption of a metal binding network by an allosteric small molecule. The Journal of Biological Chemistry. 290: 762-74 |
Lin WC, Licht S. (2014) Poly(ethylene glycol) as a scaffold for high-affinity open-channel blockers of the mouse nicotinic acetylcholine receptor. Plos One. 9: e112088 |
Deng G, Licht S, Shen J, et al. (2014) Abstract 4746: Selective inhibition of mutant IDH1 via small molecule binding to the dimer interface Cancer Research. 74: 4746-4746 |
Choi KH, Licht S. (2012) ATP-sensitive potassium channels exhibit variance in the number of open channels below the limit predicted for identical and independent gating. Plos One. 7: e37399 |
Tantama M, Licht S. (2009) Functional equivalence of the nicotinic acetylcholine receptor transmitter binding sites in the open state. Biochimica Et Biophysica Acta. 1788: 936-44 |
Farbman ME, Gershenson A, Licht S. (2008) Role of a conserved pore residue in the formation of a prehydrolytic high substrate affinity state in the AAA+ chaperone ClpA. Biochemistry. 47: 13497-505 |
Tantama M, Licht S. (2008) Use of calculated cation-pi binding energies to predict relative strengths of nicotinic acetylcholine receptor agonists. Acs Chemical Biology. 3: 693-702 |
Tantama M, Lin WC, Licht S. (2008) An activity-based protein profiling probe for the nicotinic acetylcholine receptor. Journal of the American Chemical Society. 130: 15766-7 |
Jennings LD, Lun DS, Médard M, et al. (2008) ClpP hydrolyzes a protein substrate processively in the absence of the ClpA ATPase: mechanistic studies of ATP-independent proteolysis. Biochemistry. 47: 11536-46 |
Jennings LD, Bohon J, Chance MR, et al. (2008) The ClpP N-terminus coordinates substrate access with protease active site reactivity. Biochemistry. 47: 11031-40 |