Display options
Cite
Feinberg H, Greenblatt HM, Behar V, et al. Zinc-directed inhibitors for zinc proteinases. Acta Crystallogr D Biol Crystallogr. 1995;51:428-49doi: 10.1107/S0907444995003350.
Feinberg, H., Greenblatt, H. M., Behar, V., Gilon, C., Cohen, S., Bino, A., & Shoham, G. (1995). Zinc-directed inhibitors for zinc proteinases. Acta crystallographica. Section D, Biological crystallography, 51428-49. https://doi.org/10.1107/S0907444995003350
Feinberg, H, et al. "Zinc-directed inhibitors for zinc proteinases." Acta crystallographica. Section D, Biological crystallography vol. 51 (1995): 428-49. doi: https://doi.org/10.1107/S0907444995003350
Feinberg H, Greenblatt HM, Behar V, Gilon C, Cohen S, Bino A, Shoham G. Zinc-directed inhibitors for zinc proteinases. Acta Crystallogr D Biol Crystallogr. 1995 Jul 01;51:428-49. doi: 10.1107/S0907444995003350. PMID: 15299831.
Copy Download .nbib Format: NLM
Share it on

Acta Crystallogr D Biol Crystallogr. 1995 Jul 01;51:428-49. doi: 10.1107/S0907444995003350.

Zinc-directed inhibitors for zinc proteinases.

Acta crystallographica. Section D, Biological crystallography

H Feinberg, H M Greenblatt, V Behar, C Gilon, S Cohen, A Bino, G Shoham

Affiliations

  1. Institute of Chemistry and the Laboratory of Structural Chemistry and Biology, The Hebrew University of Jerusalem, Israel.

PMID: 15299831 DOI: 10.1107/S0907444995003350

Abstract

Zinc proteinases have been recognized as a distinct class of proteolytic enzymes in which at least one ion of zinc is involved directly in catalysis. This family includes a growing number of biologically important enzymes which are attractive targets for rational drug design. In this paper we examine the special features of the zinc binding environment of these enzymes in order to gain information which could be useful in the preparation of 'zinc-directed' selective inhibitors. Carboxypeptidase A (CPA) is presented as a model for one class of zinc proteinases, and the active-site zinc and its interactions are examined with the primary focus on geometrical considerations. The three-dimensional structure of the native and apoenzyme are discussed, together with the high-resolution structure of several enzyme-inhibitor complexes. This paper will first present a structural analysis of CPA derivatives and then discuss a series of zinc model compounds which have been prepared and characterized in order to examine the ligand and geometrical preferences of the zinc in an unstrained system. X-ray crystallography (macromolecular and small molecule) is the main experimental method used for the structural analyses, while complementary computational methods have been used for the examination of electrostatic potentials. The results from the various experimental efforts are assembled in order to draw general conclusions on the potential use of the zinc ion as the primary target for inhibitor binding. The results of these studies suggest that the zinc ion is important for both the binding and the catalytic activation of the substrate as well as for stabilization of the tetrahedral reaction intermediate.

Publication Types