Selectivity of 4,5,6,7-tetrabromobenzimidazole [TBBZ] as an ATP-competitive potent inhibitor of protein kinase CK2 from various sources

• Autorzy: Zien P , Bretner M. , Zastapilo K. , Szyszka R. , Shugar D.
• Języki publikacji: EN

Słowa kluczowe

EN

Zea mays; 4,5,6,7-tetrabromobenzotriazole; crystal structure; inhibitor; protein kinase

• Wydawca: -
• Czasopismo: Cellular and Molecular Biology Letters
• Rocznik: 2003
• Tom: 08
• Numer: 2A
• Opis fizyczny: p.613-614

Twórcy

autor

Zien P

• Catholic University of Lublin, Krasnicka Av.102, 20-718 Lublin, Poland

autor

Bretner M.

autor

Zastapilo K.

autor

Szyszka R.

autor

Shugar D.

Bibliografia

• 1. Szyszka, R., Grankowski, N., Felczak, K. and Shugar D. Halogenated benzimidazoles and benzotriazoles as selective inhibitors of protein kinases CK1 and CK2 from Saccharomyces cerevisiae and other sources. Biochim. Biophys. Res. Commun. 208 (1995) 418-424.
• 2. Sarno, S., Reddy, H., Meggio, F., Rizzene, M., Davies, S.P., Donella-Deana, A., Shugar, D. and Pinna, L.A. Selectivity of 4,5,6,7- tetrabromobenzotriazole, an ATP site-directed inhibitor of protein kinase CK2 (casein kinase-2). FEBS Lett. 496 (2001) 44-48.
• 3. Battistutta, R., De Moliner, E., Sarno, S., Zanotti G. and Pinna, L.A. Structural features underlying selective inhibition of protein kinase CK2 by ATP site-directed tetrabromo-benzotriazole. Protein Sci. 10 (2001) 2200-2206.
• 4. Szyszka, R., Boguszewska, A., Shugar, D. and Grankowski, N. Halogenated benzimidazole inhibitors of phosphorylation, in vitro and in vivo, of the surface acidic proteins of the yeast ribosomal 60S subunit by endogenous protein kinases CK-II and PK60. Acta Biochim. Polon. 43 (1996) 389-396.