E. Sabini

发表

CSGID Solves Structures and Identifies Phenotypes for Five Enzymes in Toxoplasma gondii

C. Fishwick, D. Roos, Dhanasekaran Shanmugam, 2018, Front. Cell. Infect. Microbiol..

Urokinase-type plasminogen activator overexpression enhances the invasive capacity of endothelial cells.

P. Dell’Era, M. Rusnati, M. Presta, 1997, Microvascular research.

Digestion of single crystals of mannan I by an endo-mannanase from Trichoderma reesei.

K. Wilson, M. Siika‐aho, E. Sabini, 2000, European journal of biochemistry.

Crystallization and preliminary X-ray crystallographic analysis of a Trichoderma reesei beta-mannanase from glycoside hydrolase family 5.

M. Penttilä, K. Wilson, A. Brzozowski, 1999, Acta crystallographica. Section D, Biological crystallography.

Oligosaccharide binding to family 11 xylanases: both covalent intermediate and mutant product complexes display (2,5)B conformations at the active centre.

K. Wilson, G. Davies, M. Schülein, 2002, Acta crystallographica. Section D, Biological crystallography.

Nonenantioselectivity property of human deoxycytidine kinase explained by structures of the enzyme in complex with L- and D-nucleosides.

M. Konrad, A. Lavie, E. Sabini, 2007, Journal of medicinal chemistry.

Structural basis for activation of the therapeutic l-nucleoside analogs 3TC and troxacitabine by human deoxycytidine kinase

S. Burley, M. Konrad, A. Lavie, 2006, Nucleic acids research.

Extending thymidine kinase activity to the catalytic repertoire of human deoxycytidine kinase.

M. Konrad, A. Lavie, E. Sabini, 2009, Biochemistry.

Elucidation of different binding modes of purine nucleosides to human deoxycytidine kinase.

M. Konrad, A. Lavie, E. Sabini, 2008, Journal of medicinal chemistry.

Structure of human dCK suggests strategies to improve anticancer and antiviral therapy

C. Monnerjahn, M. Konrad, A. Lavie, 2003, Nature Structural Biology.

Structural basis for substrate promiscuity of dCK.

M. Konrad, A. Lavie, E. Sabini, 2008, Journal of molecular biology.

Structural basis for the preference of UTP over ATP in human deoxycytidine kinase: illuminating the role of main-chain reorganization.

M. Konrad, A. Lavie, E. Sabini, 2006, Biochemistry.

The three-dimensional structure of a Trichoderma reesei beta-mannanase from glycoside hydrolase family 5.

G Murshudov, K S Wilson, M Penttilä, 2000, Acta crystallographica. Section D, Biological crystallography.

Crystal Structures of the SpoIID Lytic Transglycosylases Essential for Bacterial Sporulation*

G. Minasov, W. Anderson, I. Dubrovska, 2016, The Journal of Biological Chemistry.

Catalysis and specificity in enzymatic glycoside hydrolysis: a 2,5B conformation for the glycosyl-enzyme intermediate revealed by the structure of the Bacillus agaradhaerens family 11 xylanase.

Z. Dauter, K. Wilson, G. Davies, 1999, Chemistry & biology.

Binding of non-catalytic ATP to human hexokinase I highlights the structural components for enzyme-membrane association control.

M. Bolognesi, G. Murshudov, C. Rosano, 1999, Structure.

Crystal structures of the components of the Staphylococcus aureus leukotoxin ED

G. Minasov, G. Grandi, W. Anderson, 2016, Acta crystallographica. Section D, Structural biology.