Di Marco S - Search Results

1

Characterization, crystallization and preliminary crystallographic analysis of human recombinant cyclooxygenase-2.

Di Marco S, Priestle JP, Grütter MG, Wennogle LP, Boyar W. Di Marco S, et al. Acta Crystallogr D Biol Crystallogr. 1997 Mar 1;53(Pt 2):224-6. doi: 10.1107/S0907444996015351. Acta Crystallogr D Biol Crystallogr. 1997. PMID: 15299964

2

Structure of recombinant human CPP32 in complex with the tetrapeptide acetyl-Asp-Val-Ala-Asp fluoromethyl ketone.

Mittl PR, Di Marco S, Krebs JF, Bai X, Karanewsky DS, Priestle JP, Tomaselli KJ, Grütter MG. Mittl PR, et al. Among authors: di marco s. J Biol Chem. 1997 Mar 7;272(10):6539-47. doi: 10.1074/jbc.272.10.6539. J Biol Chem. 1997. PMID: 9045680 Free article.

3

Refolding, isolation and characterization of crystallizable human interferon-alpha 8 expression in Saccharomyces cerevisiae.

Di Marco S, Fendrich G, Meyhack B, Grütter MG. Di Marco S, et al. J Biotechnol. 1996 Sep 13;50(1):63-73. doi: 10.1016/0168-1656(96)01550-7. J Biotechnol. 1996. PMID: 8987847

4

Recombinant hirustasin: production in yeast, crystallization, and interaction with serine proteases.

Di Marco S, Fendrich G, Knecht R, Strauss A, Pohlig G, Heim J, Priestle JP, Sommerhoff CP, Grütter MG. Di Marco S, et al. Protein Sci. 1997 Jan;6(1):109-18. doi: 10.1002/pro.5560060112. Protein Sci. 1997. PMID: 9007982 Free PMC article.

5

Purification, analysis, and enzymatic activity of recombinant human synovial fluid phospholipase A2 and N-terminal variants.

Di Marco S, Märki F, Hofstetter H, Schmitz A, van Oostrum J, Grütter MG. Di Marco S, et al. J Biochem. 1992 Sep;112(3):350-4. doi: 10.1093/oxfordjournals.jbchem.a123904. J Biochem. 1992. PMID: 1429522 Free article.

6

Mutational analysis of the structure-function relationship in interferon-alpha.

Di Marco S, Grütter MG, Priestle JP, Horisberger MA. Di Marco S, et al. Biochem Biophys Res Commun. 1994 Aug 15;202(3):1445-51. doi: 10.1006/bbrc.1994.2093. Biochem Biophys Res Commun. 1994. PMID: 8060326

7

Recombinant soluble beta-1,4-galactosyltransferases expressed in Saccharomyces cerevisiae. Purification, characterization and comparison with human enzyme.

Malissard M, Borsig L, Di Marco S, Grütter MG, Kragl U, Wandrey C, Berger EG. Malissard M, et al. Among authors: di marco s. Eur J Biochem. 1996 Jul 15;239(2):340-8. doi: 10.1111/j.1432-1033.1996.0340u.x. Eur J Biochem. 1996. PMID: 8706738 Free article.

8

A new structural class of serine protease inhibitors revealed by the structure of the hirustasin-kallikrein complex.

Mittl PR, Di Marco S, Fendrich G, Pohlig G, Heim J, Sommerhoff C, Fritz H, Priestle JP, Grütter MG. Mittl PR, et al. Among authors: di marco s. Structure. 1997 Feb 15;5(2):253-64. doi: 10.1016/s0969-2126(97)00183-4. Structure. 1997. PMID: 9032072 Free article.

9

Structure of the complex of leech-derived tryptase inhibitor (LDTI) with trypsin and modeling of the LDTI-tryptase system.

Di Marco S, Priestle JP. Di Marco S, et al. Structure. 1997 Nov 15;5(11):1465-74. doi: 10.1016/s0969-2126(97)00296-7. Structure. 1997. PMID: 9384562 Free article.

10

The 1.2 A crystal structure of hirustasin reveals the intrinsic flexibility of a family of highly disulphide-bridged inhibitors.

Usón I, Sheldrick GM, de La Fortelle E, Bricogne G, Di Marco S, Priestle JP, Grütter MG, Mittl PR. Usón I, et al. Among authors: di marco s. Structure. 1999 Jan 15;7(1):55-63. doi: 10.1016/s0969-2126(99)80009-4. Structure. 1999. PMID: 10368273 Free article.

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