Journals – 2000-1996

 

1.
De S, Galdiero S, Manco G, Lang D, Rossi M, Pedone C. A snapshot of a transition state analogue of a novel thermophilic esterase belonging to the subfamily of mammalian hormone-sensitive lipase. J Mol Biol. 2000;303(5):761-771. [PubMed]
2.
Di B, Galdiero S, Saviano M, et al. Synthesis and structural characterization of 6I,6II-diamino-6I,6II-dideoxy-cyclomaltoheptaose, a difunctionalized beta-cyclodextrin. Carbohydr Res. 1996;282(1):41-52. [PubMed]
3.
De S, Lombardi A, Galdiero S, et al. The crystal structure of a Dcp-containing peptide. Biopolymers. 2000;53(2):182-188. [PubMed]
4.
Lombardi A, De S, Galdiero S, et al. The crystal structure of Afc-containing peptides. Biopolymers. 2000;53(2):150-160. [PubMed]
5.
Lombardi A, Nastri F, Della M, et al. Rational design of true hirudin mimetics: synthesis and characterization of multisite-directed alpha-thrombin inhibitors. J Med Chem. 1996;39(10):2008-2017. [PubMed]
6.
Lombardi A, De S, Galdiero S, Staiano N, Nastri F, Pavone V. From natural to synthetic multisite thrombin inhibitors. Biopolymers. 1999;51(1):19-39. [PubMed]
7.
Lombardi A, De S, Nastri F, et al. The crystal structure of alpha-thrombin-hirunorm IV complex reveals a novel specificity site recognition mode. Protein Sci. 1999;8(1):91-95. [PubMed]
8.
Pavone V, De S, Nastri F, et al. Multiple binding mode of reversible synthetic thrombin inhibitors. A comparative structural analysis. Biol Chem. 1998;379(8-9):987-1006. [PubMed]
9.
De S, Lombardi A, Galdiero S, et al. Hirunorms are true hirudin mimetics. The crystal structure of human alpha-thrombin-hirunorm V complex. Protein Sci. 1998;7(2):243-253. [PubMed]