Screening for Dimerization Inhibitors for Bacterial Acetyl CoA Carboxylase
- Sandia National Laboratories (SNL), Albuquerque, NM, and Livermore, CA (United States)
- Louisiana State University, Baton Rouge, LA (United States)
The goal of this project was to develop compounds that kill biothreat bacteria by inhibiting the activity of bacterial acetyl CoA carboxylase (ACC) by blocking dimerization of one component of that enzyme complex, biotin carboxylase (BC). The ultimate goal is to combine a BC dimerization inhibitor with an existing active site inhibitor for carboxytransferase, another component of ACC, to form a new dual inhibitor therapy for this essential enzyme to avoid onset of resistance. Developing medical countermeasures to defeat antibiotic resistance in biothreat agents is of interest for national security for protecting both warfighters and the public.
- Research Organization:
- Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States); Sandia National Laboratories (SNL-CA), Livermore, CA (United States)
- Sponsoring Organization:
- USDOE National Nuclear Security Administration (NNSA); USDOE Laboratory Directed Research and Development (LDRD) Program
- DOE Contract Number:
- AC04-94AL85000; NA0003525
- OSTI ID:
- 1573932
- Report Number(s):
- SAND--2019-13612R; 681227
- Country of Publication:
- United States
- Language:
- English
Similar Records
Crystal structure of the 500-kDa yeast acetyl-CoA carboxylase holoenzyme dimer
Is Dimerization Required for the Catalytic Activity of Bacterial Biotin Carboxylase?
Purification and characterization of acetyl-CoA carboxylase from the Diatom Cyclotella cryptica
Journal Article
·
Mon Oct 12 00:00:00 EDT 2015
· Nature (London)
·
OSTI ID:1354314
Is Dimerization Required for the Catalytic Activity of Bacterial Biotin Carboxylase?
Journal Article
·
Sat Dec 31 23:00:00 EST 2005
· Mol. Cell
·
OSTI ID:914025
Purification and characterization of acetyl-CoA carboxylase from the Diatom Cyclotella cryptica
Journal Article
·
Sun Dec 31 23:00:00 EST 1989
· Plant Physiology; (USA)
·
OSTI ID:7192093