Marc S. Cortese, Ph.D.
Affiliations: | 2001 | University of Idaho, Moscow, ID, United States |
Area:
Microbiology Biology, Molecular Biology, BiogeochemistryGoogle:
"Marc Cortese"Mean distance: 7238.73
Parents
Sign in to add mentor| Ronald Lyle Crawford | grad student | 2001 | University of Idaho | |
| (Function and origin of pyridine -2,6 -bis(thiocarboxylic acid).) | ||||
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Publications
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| Johnson DE, Xue B, Sickmeier MD, et al. (2012) High-throughput characterization of intrinsic disorder in proteins from the Protein Structure Initiative. Journal of Structural Biology. 180: 201-15 |
| Leppard KN, Emmott E, Cortese MS, et al. (2009) Adenovirus type 5 E4 Orf3 protein targets promyelocytic leukaemia (PML) protein nuclear domains for disruption via a sequence in PML isoform II that is predicted as a protein interaction site by bioinformatic analysis. The Journal of General Virology. 90: 95-104 |
| Cortese MS, Uversky VN, Dunker AK. (2008) Intrinsic disorder in scaffold proteins: getting more from less. Progress in Biophysics and Molecular Biology. 98: 85-106 |
| Hurley TD, Yang J, Zhang L, et al. (2007) Structural basis for regulation of protein phosphatase 1 by inhibitor-2. The Journal of Biological Chemistry. 282: 28874-83 |
| Vacic V, Oldfield CJ, Mohan A, et al. (2007) Characterization of molecular recognition features, MoRFs, and their binding partners. Journal of Proteome Research. 6: 2351-66 |
| Le Gall T, Romero PR, Cortese MS, et al. (2007) Intrinsic disorder in the Protein Data Bank. Journal of Biomolecular Structure & Dynamics. 24: 325-42 |
| Sickmeier M, Hamilton JA, LeGall T, et al. (2007) DisProt: the Database of Disordered Proteins. Nucleic Acids Research. 35: D786-93 |
| Mohan A, Oldfield CJ, Radivojac P, et al. (2006) Analysis of molecular recognition features (MoRFs). Journal of Molecular Biology. 362: 1043-59 |
| Cheng Y, LeGall T, Oldfield CJ, et al. (2006) Rational drug design via intrinsically disordered protein. Trends in Biotechnology. 24: 435-42 |
| Romero PR, Zaidi S, Fang YY, et al. (2006) Alternative splicing in concert with protein intrinsic disorder enables increased functional diversity in multicellular organisms. Proceedings of the National Academy of Sciences of the United States of America. 103: 8390-5 |