Charles E. Bugg
Affiliations: | 1968-1993 | University of Alabama, Birmingham, Birmingham, AL, United States |
Website:
https://history.amercrystalassn.org/h-bugg_homeGoogle:
"Charles Edward Bugg" OR "Charles E Bugg"Bio:
https://www.proquest.com/openview/ec87c88213fc52ea3de97ffae23310c5/1
Parents
Sign in to add mentor| Ronald L. Sass | grad student | 1965 | Rice University (Evolution Tree) | |
| (The Crystal Structures of Pyridinium Dicyanomethylide and Potassium Paranitrophenyldicyanomethide) | ||||
| Robert B. Corey | post-doc | 1956-1966 | Caltech (Chemistry Tree) | |
| Richard E. Marsh | post-doc | 1965-1966 | Caltech (Chemistry Tree) | |
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Publications
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| Suddath FL, Bugg CE, Ealick SA, et al. (2010) The 1.3-A Structure of a Scorpion Neurotoxin: A Membrane-binding Protein. Biophysical Journal. 37: 185-6 |
| Narayana SV, Bugg CE, Ealick SE. (1997) Refined structure of purine nucleoside phosphorylase at 2.75 A resolution. Acta Crystallographica. Section D, Biological Crystallography. 53: 131-42 |
| Babu YS, Ealick SE, Bugg CE, et al. (1995) Structure-based design of inhibitors of purine nucleoside phosphorylase. Acta Crystallographica. Section D, Biological Crystallography. 51: 529-35 |
| Carson M, Bugg CE, DeLucas LJ, et al. (1994) Comparison of homology models with the experimental structure of a novel serine protease. Acta Crystallographica. Section D, Biological Crystallography. 50: 889-99 |
| Long MM, DeLucas LJ, Smith C, et al. (1994) Protein crystal growth in microgravity temperature induced large scale crystallization of insulin Microgravity Science and Technology. 7: 196-202 |
| Narayana SVL, Carson M, El-Kabbani O, et al. (1994) Structure of human factor D: A complement system protein at 2.0 Å resolution Journal of Molecular Biology. 235: 695-708 |
| Guida WC, Elliott RD, Thomas HJ, et al. (1994) Structure-based design of inhibitors of purine nucleoside phosphorylase. 4. A study of phosphate mimics. Journal of Medicinal Chemistry. 37: 1109-14 |
| Secrist JA, Niwas S, Rose JD, et al. (1993) Structure-based design of inhibitors of purine nucleoside phosphorylase. 2. 9-Alicyclic and 9-heteroalicyclic derivatives of 9-deazaguanine. Journal of Medicinal Chemistry. 36: 1847-54 |
| Montgomery JA, Niwas S, Rose JD, et al. (1993) Structure-based design of inhibitors of purine nucleoside phosphorylase. 1. 9-(arylmethyl) derivatives of 9-deazaguanine. Journal of Medicinal Chemistry. 36: 55-69 |
| Ealick SE, Babu YS, Bugg CE, et al. (1993) Application of X-ray crystallographic methods in the design of purine nucleoside phosphorylase inhibitors. Annals of the New York Academy of Sciences. 685: 237-47 |