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Research Topic : Enzyme
Scheme : NHMRC Project Grants
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Enzymes (8)
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  • Funded Activity

    Enzymes That Build Up Plaque On Teeth

    Funder
    National Health and Medical Research Council
    Funding Amount
    $176,350.00
    More information
    Funded Activity

    Inhibitors Of Cell Replication As Potential Anticancer Drugs

    Funder
    National Health and Medical Research Council
    Funding Amount
    $298,847.00
    More information
    Funded Activity

    Control Of Heme Synthesis And Its Relation To Diseases

    Funder
    National Health and Medical Research Council
    Funding Amount
    $189,942.00
    More information
    Funded Activity

    Expression And Regulation Of Some Drug Metabolizing Enz Ymes In Human Liver

    Funder
    National Health and Medical Research Council
    Funding Amount
    $166,316.00
    More information
    Funded Activity

    Dual Effects Of Cimetidine On Hepatic Drug Metabolism

    Funder
    National Health and Medical Research Council
    Funding Amount
    $84,529.00
    More information
    Funded Activity

    Probing UDP-glucuronosyltransferase Protein-protein Interactions: The Power Of Two.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $482,710.00
    Summary
    Drugs and other chemicals (eg. dietary constituents, environmental pollutants, and chemicals that occur naturally in the body - such as steroid hormones) are broken down by specialised proteins called enzymes. This process is referred to as biotransformation, or 'metabolism'. Drug and chemical metabolism serves as a detoxification mechanism (since the products of metabolism generally lack biological activity) and as a means of eliminating these substances from the body. UDP-Glucuronosyltransfera .... Drugs and other chemicals (eg. dietary constituents, environmental pollutants, and chemicals that occur naturally in the body - such as steroid hormones) are broken down by specialised proteins called enzymes. This process is referred to as biotransformation, or 'metabolism'. Drug and chemical metabolism serves as a detoxification mechanism (since the products of metabolism generally lack biological activity) and as a means of eliminating these substances from the body. UDP-Glucuronosyltransferase (UGT) is one of the most important enzymes involved in drug and chemical metabolism. Consistent with its ability to metabolise such a large number of compounds, UGT is known to exist as a 'superfamily' of structurally related proteins. Despite the importance of UGT, little is known about the structural characteristics of these enzymes that are responsible for recognising and binding different classes of chemicals. Accumulating evidence from this and other laboratories indicates that the individual UGT proteins may combine with themselves (to form a homodimer) and with other UGT proteins (to form heterodimers). This project largely seeks to define the scope of UGT homo- and hetero- dimerisation, identify the structural elements of the proteins responsible for association and characterise the functional significance of dimerisation. The project will further explore associations between UGTs and other proteins, namely albumin. Characterisation of UGT dimerisation and associations with other proteins is fundamental to our understanding of how this enzyme functions and selects particular chemicals for metabolism. The work also has important implications for the devlopment and interpretation of in vitro (or 'test-tube') approaches for predicting how drugs are metabolised in humans. Such tests are widely employed in research and pharmaceutical company laboratories to predict how the body 'handles' new drugs prior to their administration to humans.
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    Funded Activity

    The Molecular Mechanism Of Sphingosine Kinase Activation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $442,500.00
    Summary
    Many cell processes like growth, death and differentiation are controlled by hormones and other molecules that interact with receptors on the outside of the cell. When this type of molecule binds to a receptor, it often triggers the production of signaling molecules inside the cell that initiate a change in the cells behaviour. The lipid molecule, sphingosine phosphate has been identified as such a signaling molecule that appears to be involved in the regulation of a diverse array of important m .... Many cell processes like growth, death and differentiation are controlled by hormones and other molecules that interact with receptors on the outside of the cell. When this type of molecule binds to a receptor, it often triggers the production of signaling molecules inside the cell that initiate a change in the cells behaviour. The lipid molecule, sphingosine phosphate has been identified as such a signaling molecule that appears to be involved in the regulation of a diverse array of important mammalian cellular processes. Recent studies have found that sphingosine phosphate is involved in the inflammation of cells, and if its production can be blocked, inflammation is not seen. Therefore, this provides a potential target for therapeutic intervention in the inflammation process. However, the manner by which cells regulate sphingosine phosphate levels is not well known. It is known that sphingosine phosphate is produced by the enzyme sphingosine kinase, and strong evidence suggests that changes in this enzyme's activity in the cell regulate sphingosine phosphate levels. However, how the cell changes the levels of sphingosine kinase activity is completely unknown. This study will investigate this problem with the view that understanding this process will allow the development of new drugs to block increases in sphingosine kinase activity, preventing increases in sphingosine phosphate levels, and it turn, preventing cellular inflammation.
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    Funded Activity

    Properties Of An Enzyme That Degrades Glycosaminoglycan S

    Funder
    National Health and Medical Research Council
    Funding Amount
    $84,300.00
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    Funded Activity

    Src-family And CSK Family Of Tyrosine Kinases

    Funder
    National Health and Medical Research Council
    Funding Amount
    $167,630.00
    More information
    Funded Activity

    Evolution And Targeting Of Polysaccharide Biosynthesis In Leishmania Parasites

    Funder
    National Health and Medical Research Council
    Funding Amount
    $449,484.00
    Summary
    Leishmania are parasitic protozoa that cause devastating diseases in humans. This proposal will identify the enzymes involved in the biosynthesis of an unusual carbohydrate reserve material that accumulates in pathogenic stages of these parasites. Information on the structure and mode of action of these enzymes will be used to develop novel drugs that will be tested for anti-parasite activity.
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