Display Settings:

Format

Send to:

Choose Destination

    J Mol Biol. 2002 May 10;318(4):1009-17.

    The X-ray crystallographic structure of the angiogenesis inhibitor angiostatin.

    Abad MC, Arni RK, Grella DK, Castellino FJ, Tulinsky A, Geiger JH.

    Department of Chemistry, Michigan State University, East Lansing 48824, USA.

    Angiogenesis inhibitors have gained much public attention recently as anti-cancer agents and several are currently in clinical trials, including angiostatin (Phase I, Thomas Jefferson University Hospital, Philadelphia, PA). We report here the bowl-shaped structure of angiostatin kringles 1-3, the first multi-kringle structure to be determined. All three kringle lysine-binding sites contain a bound bicine molecule of crystallization while the former of kringle 2 and kringle 3 are cofacial. Moreover, the separation of the kringle 2 and kringle 3 lysiner binding sites is sufficient to accommodate the alpha-helix of the 30 residue peptide VEK-30 found in the kringle 2/VEK-30 complex. Together the three kringles produce a central cavity suggestive of a unique domain where they may function in concert. (c) 2002 Elsevier Science Ltd.

    PMID: 12054798 [PubMed - indexed for MEDLINE]

    Supplemental Content

    Click here to read

    Structures reported by this article