Small peptide inhibitors of acetyl-peptide hydrolase having an uncommon mechanism of inhibition and a stable bent conformation(423 views visite) Sandomenico A, Russo A, Palmieri G, Bergamo P, Gogliettino M, Falcigno L, Ruvo M
J Med Chem (ISSN: 0022-2623, 1520-4804, 0022-2623print), 2012 Mar 8; 55(5): 2102-2111.
Istituto di Biostrutture e Bioimmagini, CNR, via Mezzocannone 16, 80134, Napoli, Italy Istituto di Biochimica Delle Proteine, CNR, via P. Castellino, 111, 80132, Napoli, Italy Istituto di Scienze Degli Alimenti, CNR, via Roma 64, 83100, Avellino, Italy Dipartimento di Scienze Chimiche, Università di Napoli Federico II, via Cinthia, 80143, Napoli, Italy
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Orlowski, R. Z., Kuhn, D. J., Proteasome inhibitors in cancer therapy: Lessons from the first decade (2008) Clin. Cancer Res., 14, pp. 1649-1657
Landis-Piwowar, K. R., Milacic, V., Chen, D., Yang, H., Zhao, Y., Chan, T. H., Yan, B., Dou, Q. P., The proteasome as a potential target for novel anticancer drugs and chemosensitizers (2006) Drug Resist. Updates, 9, pp. 263-273
Segel, I. H., (1975) Enzyme Kinetics, pp. 161-166. , Wiley Interscience: New York
Wishart, D. S., Sykes, B. D., Richards, F. M., Relationship between nuclear magnetic resonance chemical shift and protein secondary structure (1991) J. Mol. Biol., 222, pp. 311-333
Moerschell, R. P., Hosokawa, Y., Tsunasawa, S., Sherman, F., The specificities of yeast methionine aminopeptidase and acetylation of amino-terminal methionine in vivo. Processing of altered iso-1-cytochromes c created by oligonucleotide transformation (1990) J. Biol. Chem., 265, pp. 19638-19643
Constam, D. B., Tobler, A. R., Rensing-Ehl, A., Kemler, I., Hersh, L. B., Fontana, A., Puromycin-sensitive aminopeptidase. Sequence analysis, expression, and functional characterization (1995) J. Biol. Chem., 270, pp. 26931-26939
Moore, H. E., Davenport, E. L., Smith, E. M., Muralikrishnan, S., Dunlop, A. S., Walker, B. A., Krige, D., Davies, F. E., Aminopeptidase inhibition as a targeted treatment strategy in myeloma (2009) Mol. Cancer Ther., 8, pp. 762-770
Casida, J. E., Quistad, G. B., Serine hydrolase targets of organophosphorus toxicants (2005) Chem. Biol. Interact., 157-158, pp. 277-283
Westley, A. M., Westley, J., Enzyme inhibition in open systems. Superiority of uncompetitive agents (1996) J. Biol. Chem., 271, pp. 5347-52
Fields, G. B., Noble, R. L., Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids (1990) Int. J. Pept. Protein Res., 35, pp. 161-214
Small peptide inhibitors of acetyl-peptide hydrolase having an uncommon mechanism of inhibition and a stable bent conformation
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