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Functions and mechanisms of M. tuberculosis S/T kinases

Functions and mechanisms of M. tuberculosis S/T kinases
结核分枝杆菌S/T激酶的功能和机制
批准号:
7010036
负责人:
THOMAS C ALBER
金额:
$25.25万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-03-01 至 2009-02-28

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The long-term goal of this proposed program is to understand the functions of Ser/Thr protein kinases (STPKs) recently discovered in Mycobacterium tuberculosis (Mtb). This pathogenic bacterium, which is the causative agent of tuberculosis (TB), infects one third of the world's population. TB kills over 3 million people annually, more than any other infectious disease. Despite the large amount of work on protein kinases and phosphatases, little is known about the roles of the Mtb STPKs and the single Mtb Ser/Thr phosphatase, Ppp. Research to define the specific biological functions of these enzymes is needed to know how environmental signals regulate Mtb metabolism. We will focus biochemical, biophysical, structural and genetic methods principally on four Mtb proteins. This research has four specific aims: 1. Define the basis for signaling in two Mtb transmembrane receptor kinases. 2. Define the mechanism of PknB kinase switching between off and on states. 3. Discover protein substrates of Mtb STPKs. 4. Define the intracellular signaling pathways, focusing on the single Mtb Ser/Thr phosphatase, Ppp. Our preliminary studies established the feasibility of these aims. Our biochemical and structural work on the kinase domain of Mtb PknB showed that the prokaryotic and eukaryotic STPKs share a remarkably conserved three-dimensional structure and universal mechanisms of regulation and substrate recognition. We determined the first crystal structures of a bacterial STPK sensor domain and bacterial Ser/Thr phosphatase. We have set the stage to define the active and inactive states of the PknB kinase. Our proposed exploration of the substrates of PknB and Ppp will begin to define the functions of these proteins. Because of the central roles of kinase signaling in cellular physiology, the increasing focus on STPKs as pharmaceutical targets, and the worldwide health impact of TB, our proposed studies will have high significance for molecular biology and medicine.
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Vulnerabilities in Mycobacterial Cell-Wall Biogenesis
  • 批准号:
    8353014
  • 项目类别:
  • 资助金额:
    $41.02万
  • 财政年份:
    2012
  • 负责人:
    THOMAS C ALBER
  • 依托单位:
ROLE OF PROTEIN SOFT SPOTS IN LIGAND RECOGNITION AND INHIBITOR DESIGN
ROLE OF PROTEIN SOFT SPOTS IN LIGAND RECOGNITION AND INHIBITOR DESIGN
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