Sfoglia per Autore
Biochemical and three-dimensional-structural study of the specific inhibition of protein kinase CK2 by [5-oxo-5,6-dihydroindolo-(1,2-a)quinazolin-7-yl]acetic acid (IQA)
2003 Sarno, Stefania; DE MOLINER, Erika; Ruzzene, Maria; Pagano, MARIO ANGELO PRIMO; Battistutta, Roberto; Bain, J.; Fabbro, D.; Schoepfer, J.; Elliott, M.; Furet, P.; Meggio, Flavio; Zanotti, Giuseppe; Pinna, Lorenzo
Structural features of protein kinase CK2.
2002 Zanotti, Giuseppe; Battistutta, Roberto; DE MOLINER, Erika; Sarno, Stefania; Pinna, Lorenzo
Structural features underlying selective inhibition of protein kinase CK2 by ATP site-directed tetrabromo-2-benzotriazole
2001 Battistutta, Roberto; DE MOLINER, Erika; Sarno, Stefania; Zanotti, Giuseppe; Pinna, Lorenzo
Structural basis for selective inhibition of protein kinase CK2 by ATP site-directed ligands
2001 Sarno, Stefania; Battistutta, Roberto; DE MOLINER, Erika; Meggio, Flavio; Zanotti, Giuseppe; Pinna, Lorenzo
The Replacement of ATP by the Competitive Inhibitor Emodin Induces Conformational Modifications in the Catalytic Site of Protein Kinase CK2
2000 Battistutta, Roberto; Sarno, Stefania; DE MOLINER, Erika; Papinutto, Elena; Zanotti, Giuseppe; Pinna, Lorenzo
The crystal structure of the complex of Zea mays alpha subunit with a fragment of human beta subunit provides the clue to the architecture of protein kinase CK2 holoenzyme.
2000 Battistutta, Roberto; Sarno, Stefania; DE MOLINER, Erika; Marin, Oriano; Issinger, O. G.; Zanotti, Giuseppe; Pinna, Lorenzo
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