The long-term objective of this proposal is to define the structure- function relation in the E. coli enzyme, glutamine-dependent carbamyl phosphate synthetase (CPS). This enzyme with a unique mechanism of catalysis synthesizes a high energy precursor (carbamyl phosphate), required for pyrimidine biosynthesis in all living organisms. The protein has a complex mosaic structure with active sites related to the biotin-dependent carboxylases, and to a large family of enzymes that provide amide nitrogen for diverse biosynthetic reactions. At present, very little is known about these multifunctional enzymes and the manner in which their different active sites spatially and temporally interact during conversion of substrate to products.
The specific aims are: (1) to continue the structure determination of E coli CPS by X-ray and multiwavelength anomalous diffraction analysis in a collaborative arrangement with Dr. Wayne Hendrickson's laboratory to solve the crystal structure; (2) to determine the structure of different catalytic and conformational forms of the protein; (3) to identify the functions of essential catalytic residues at each of the two ATP binding sites from hypotheses generated by the structure. Catalytic site mutants impaired in active site coupling are anticipated to provide additional mechanistic details of carbamate synthesis and phosphorylation; (4) to define residues essential to the function of the glutamine hydrolytic site, through site modification and kinetic analysis of thioester and product formation. New insights derived from the three-dimensional structure of CPS bear directly on the field of molecular medicine. Lesions in the human NH3-dependent enzyme either are lethal or lead to hyperammonemia, hepatic coma, and CNS damage. New directed enzyme therapies are continually being developed. Human pyrimidine-specific CPS is highly elevated in rapidly proliferating tumor tissue, and, therefore is a prime candidate for design of potent and selective inhibitors of the rapid tissue growth associated with cancer.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM025846-19
Application #
2857080
Study Section
Physical Biochemistry Study Section (PB)
Project Start
1980-04-01
Project End
2001-12-31
Budget Start
1999-01-01
Budget End
1999-12-31
Support Year
19
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Public Health Research Institute
Department
Type
DUNS #
City
Newark
State
NJ
Country
United States
Zip Code
07103
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Hong, J; Salo, W L; Lusty, C J et al. (1994) Carbamyl phosphate synthetase III, an evolutionary intermediate in the transition between glutamine-dependent and ammonia-dependent carbamyl phosphate synthetases. J Mol Biol 243:131-40
Bueso, J; Lusty, C J; Rubio, V (1994) Location of the binding site for the allosteric activator IMP in the COOH-terminal domain of Escherichia coli carbamyl phosphates synthetase. Biochem Biophys Res Commun 203:1083-9
Cervera, J; Conejero-Lara, F; Ruiz-Sanz, J et al. (1993) The influence of effectors and subunit interactions on Escherichia coli carbamoyl-phosphate synthetase studied by differential scanning calorimetry. J Biol Chem 268:12504-11
Lusty, C J; Liao, M (1993) Substitution of Glu841 by lysine in the carbamate domain of carbamyl phosphate synthetase alters the catalytic properties of the glutaminase subunit. Biochemistry 32:1278-84
Kern, C B; Lusty, C J; Davidson, J N (1992) Evidence that mammalian glutamine-dependent carbamyl phosphate synthetase arose through gene fusion. J Mol Evol 35:217-22
Guillou, F; Liao, M; Garcia-Espana, A et al. (1992) Mutational analysis of carbamyl phosphate synthetase. Substitution of Glu841 leads to loss of functional coupling between the two catalytic domains of the synthetase subunit. Biochemistry 31:1656-64
Lusty, C J (1992) Detection of an enzyme bound gamma-glutamyl acyl ester of carbamyl phosphate synthetase of Escherichia coli. FEBS Lett 314:135-8
Mullins, L S; Lusty, C J; Raushel, F M (1991) Alterations in the energetics of the carbamoyl phosphate synthetase reaction by site-directed modification of the essential sulfhydryl group. J Biol Chem 266:8236-40
Rubio, V; Cervera, J; Lusty, C J et al. (1991) Domain structure of the large subunit of Escherichia coli carbamoyl phosphate synthetase. Location of the binding site for the allosteric inhibitor UMP in the COOH-terminal domain. Biochemistry 30:1068-75

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