Pessi A - Search Results

1

Selection of potent inhibitors of farnesyl-protein transferase from a synthetic tetrapeptide combinatorial library.

Wallace A, Koblan KS, Hamilton K, Marquis-Omer DJ, Miller PJ, Mosser SD, Omer CA, Schaber MD, Cortese R, Oliff A, Gibbs JB, Pessi A. Wallace A, et al. Among authors: pessi a. J Biol Chem. 1996 Dec 6;271(49):31306-11. doi: 10.1074/jbc.271.49.31306. J Biol Chem. 1996. PMID: 8940136 Free article.

2

A Multimeric Synthetic Peptide Combinatorial Library.

Wallace A, Altamura S, Toniatti C, Vitelli A, Bianchi E, Delmastro P, Ciliberto G, Pessi A. Wallace A, et al. Among authors: pessi a. Pept Res. 1994 Jan-Feb;7(1):27-31. Pept Res. 1994. PMID: 8019059

3

Conformation of a novel tetrapeptide inhibitor NH2-D-Trp-D-Met-Phe(pCl)-Gla-NH2 bound to farnesyl-protein transferase.

Bogusky MJ, Culberson JC, Pitzenberger SM, Garsky VM, Wallace A, Pessi A, Koblan KS. Bogusky MJ, et al. Among authors: pessi a. J Pept Res. 1999 Jul;54(1):66-73. doi: 10.1034/j.1399-3011.1999.00085.x. J Pept Res. 1999. PMID: 10448971

4

Ligands for kappa-opioid and ORL1 receptors identified from a conformationally constrained peptide combinatorial library.

Becker JA, Wallace A, Garzon A, Ingallinella P, Bianchi E, Cortese R, Simonin F, Kieffer BL, Pessi A. Becker JA, et al. Among authors: pessi a. J Biol Chem. 1999 Sep 24;274(39):27513-22. doi: 10.1074/jbc.274.39.27513. J Biol Chem. 1999. PMID: 10488086 Free article.

5

Potent peptide inhibitors of human hepatitis C virus NS3 protease are obtained by optimizing the cleavage products.

Ingallinella P, Altamura S, Bianchi E, Taliani M, Ingenito R, Cortese R, De Francesco R, Steinkühler C, Pessi A. Ingallinella P, et al. Among authors: pessi a. Biochemistry. 1998 Jun 23;37(25):8906-14. doi: 10.1021/bi980314n. Biochemistry. 1998. PMID: 9636032

6

Prime site binding inhibitors of a serine protease: NS3/4A of hepatitis C virus.

Ingallinella P, Fattori D, Altamura S, Steinkühler C, Koch U, Cicero D, Bazzo R, Cortese R, Bianchi E, Pessi A. Ingallinella P, et al. Among authors: pessi a. Biochemistry. 2002 Apr 30;41(17):5483-92. doi: 10.1021/bi025603x. Biochemistry. 2002. PMID: 11969409

7

Mimicking of discontinuous epitopes by phage-displayed peptides, I. Epitope mapping of human H ferritin using a phage library of constrained peptides.

Luzzago A, Felici F, Tramontano A, Pessi A, Cortese R. Luzzago A, et al. Among authors: pessi a. Gene. 1993 Jun 15;128(1):51-7. doi: 10.1016/0378-1119(93)90152-s. Gene. 1993. PMID: 7685301

8

Product inhibition of the hepatitis C virus NS3 protease.

Steinkühler C, Biasiol G, Brunetti M, Urbani A, Koch U, Cortese R, Pessi A, De Francesco R. Steinkühler C, et al. Among authors: pessi a. Biochemistry. 1998 Jun 23;37(25):8899-905. doi: 10.1021/bi980313v. Biochemistry. 1998. PMID: 9636031

9

Structural characterization of the interactions of optimized product inhibitors with the N-terminal proteinase domain of the hepatitis C virus (HCV) NS3 protein by NMR and modelling studies.

Cicero DO, Barbato G, Koch U, Ingallinella P, Bianchi E, Nardi MC, Steinkühler C, Cortese R, Matassa V, De Francesco R, Pessi A, Bazzo R. Cicero DO, et al. Among authors: pessi a. J Mol Biol. 1999 Jun 4;289(2):385-96. doi: 10.1006/jmbi.1999.2746. J Mol Biol. 1999. PMID: 10366512

10

A loop-mimetic inhibitor of the HCV-NS3 protease derived from a minibody.

Martin F, Steinkühler C, Brunetti M, Pessi A, Cortese R, De Francesco R, Sollazzo M. Martin F, et al. Among authors: pessi a. Protein Eng. 1999 Nov;12(11):1005-11. doi: 10.1093/protein/12.11.1005. Protein Eng. 1999. PMID: 10585507

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