Skip NavigationSkip to Content

Insights Into the Structure of Hepatocyte Growth Factor Scatter Factor (Hgf/Sf) and Implications For Receptor Activation

  1. Author:
    Chirgadze, D. Y.
    Hepple, J.
    Byrd, R. A.
    Sowdhamini, R.
    Blundell, T. L.
    Gherardi, E.
    1. Year: 1998
  1. Journal: Febs Letters
    1. 430
    2. 1-2 Special Issue SI
    3. Pages: 126-129
  2. Type of Article: Article
  1. Abstract:

    The modular structure of HGF/SF offers a reductionist or 'divide and rule' approach to the analysis of structure and function. Domain deletion experiments have established that the N domain, kringle 1 and kringle 2 are essential for HGF/SF activity and that truncated variants containing the N domain and kringle 1 (NK1) or kringles 1 and 2 (NK2) can exhibit partial agonistic or antagonistic activity depending on target cells. Comparative modelling has been used to predict the 3D structures of the six domains of HGF/SF, More recently, NMR methods have shown that the N domain has a novel fold, the charge distribution of which suggests a heparin binding site. Crystals of NK1 indicate the relationship of this domain to the kringle 1, offering further insights into the mechanism of domain interactions and receptor activation. (C) 1998 Federation of European Biochemical Societies. [References: 25]

    See More

External Sources

  1. No sources found.

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel