This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Natural products, including terpenoids, have historically provided the compounds used most successfully as leads for pharmaceutical, agricultural, and other commercial applications. The objectives of our research is to understand the structural, functional and chemical features governing: 1) the biosynthesis of IPP, the universal building unit for the biosynthesis of isoprenoids, via the recently discovered MEP pathway, involving the proteins DXS, DXR, YgbP, YchB, YgbB, GcpE and LytB 2) the conversion of IPP to its isomer, DMAPP, by type II IPP isomerases 3) the catalysis of FPPS enzyme 3) the mechanisms of FPP cyclization by terpene cyclases.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001209-27
Application #
7370389
Study Section
Special Emphasis Panel (ZRG1-BPC-E (40))
Project Start
2006-03-01
Project End
2007-02-28
Budget Start
2006-03-01
Budget End
2007-02-28
Support Year
27
Fiscal Year
2006
Total Cost
$3,003
Indirect Cost
Name
Stanford University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Lal, Neeraj K; Nagalakshmi, Ugrappa; Hurlburt, Nicholas K et al. (2018) The Receptor-like Cytoplasmic Kinase BIK1 Localizes to the Nucleus and Regulates Defense Hormone Expression during Plant Innate Immunity. Cell Host Microbe 23:485-497.e5
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