From Wikipedia, the free encyclopedia
Carbamoyl-phosphate synthetase (glutamine-hydrolysing)
Identifiers
EC no. 6.3.5.5
CAS no. 37233-48-0
Databases
IntEnz IntEnz view
BRENDA BRENDA entry
ExPASy NiceZyme view
KEGG KEGG entry
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Search
PMC articles
PubMed articles
NCBI proteins
carbamoyl-phosphate synthetase 1, aspartate transcarbamylase, and dihydroorotase
Identifiers
SymbolCAD
NCBI gene 790
HGNC 1424
OMIM 114010
RefSeq NM_004341
UniProt P27708
Other data
Locus Chr. 2 p21
Search for
Structures Swiss-model
Domains InterPro

Carbamoyl phosphate synthetase (glutamine-hydrolysing) ( EC 6.3.5.5) is an enzyme that catalyzes the reactions that produce carbamoyl phosphate in the cytosol (as opposed to type I, which functions in the mitochondria). Its systemic name is hydrogen-carbonate:L-glutamine amido-ligase (ADP-forming, carbamate-phosphorylating). [1] [2] [3] [4] [5] [6] [7] [8]

In pyrimidine biosynthesis, it serves as the rate-limiting enzyme and catalyzes the following reaction:

2 ATP + L- glutamine + HCO3 + H2O 2 ADP + phosphate + L- glutamate + carbamoyl phosphate (overall reaction)
(1a) L-glutamine + H2O L-glutamate + NH3
(1b) 2 ATP + HCO3 + NH3 2 ADP + phosphate + carbamoyl phosphate

It is activated by ATP and PRPP [9] and it is inhibited by UTP (Uridine triphosphate) [10] Neither CPSI nor CPSII require biotin as a coenzyme, as seen with most carboxylation reactions.

It is one of the three enzyme functions coded by the CAD gene. It is classified under EC 6.3.5.5.

See also

References

  1. ^ Anderson PM, Meister A (December 1965). "Evidence for an activated form of carbon dioxide in the reaction catalyzed by Escherichia coli carbamyl phosphate synthetase". Biochemistry. 4 (12): 2803–9. doi: 10.1021/bi00888a034. PMID  5326356.
  2. ^ Kalman SM, Duffield PH, Brzozowski T (April 1966). "Purification and properties of a bacterial carbamyl phosphate synthetase". The Journal of Biological Chemistry. 241 (8): 1871–7. doi: 10.1016/S0021-9258(18)96716-5. PMID  5329589.
  3. ^ Yip MC, Knox WE (May 1970). "Glutamine-dependent carbamyl phosphate synthetase. Properties and distribution in normal and neoplastic rat tissues". The Journal of Biological Chemistry. 245 (9): 2199–204. doi: 10.1016/S0021-9258(18)63139-4. PMID  5442268.
  4. ^ Stapleton MA, Javid-Majd F, Harmon MF, Hanks BA, Grahmann JL, Mullins LS, Raushel FM (November 1996). "Role of conserved residues within the carboxy phosphate domain of carbamoyl phosphate synthetase". Biochemistry. 35 (45): 14352–61. doi: 10.1021/bi961183y. PMID  8916922.
  5. ^ Holden HM, Thoden JB, Raushel FM (December 1998). "Carbamoyl phosphate synthetase: a tunnel runs through it". Current Opinion in Structural Biology. 8 (6): 679–85. doi: 10.1016/s0959-440x(98)80086-9. PMID  9914247.
  6. ^ Raushel FM, Thoden JB, Reinhart GD, Holden HM (October 1998). "Carbamoyl phosphate synthetase: a crooked path from substrates to products". Current Opinion in Chemical Biology. 2 (5): 624–32. doi: 10.1016/s1367-5931(98)80094-x. PMID  9818189.
  7. ^ Raushel FM, Thoden JB, Holden HM (June 1999). "The amidotransferase family of enzymes: molecular machines for the production and delivery of ammonia". Biochemistry. 38 (25): 7891–9. doi: 10.1021/bi990871p. PMID  10387030.
  8. ^ Thoden JB, Huang X, Raushel FM, Holden HM (October 2002). "Carbamoyl-phosphate synthetase. Creation of an escape route for ammonia". The Journal of Biological Chemistry. 277 (42): 39722–7. doi: 10.1074/jbc.M206915200. PMID  12130656.
  9. ^ Inkling. "Unsupported Browser". Inkling. Retrieved 25 April 2018.
  10. ^ Engelking LR. Pyrimidine biosynthesis. Textbook of Veterinary Physiological Chemistry. 2015;:83–7. https://doi.org/10.1016/B978-0-12-391909-0.50014-1 Retrieved 1 April 2023

External links


From Wikipedia, the free encyclopedia
Carbamoyl-phosphate synthetase (glutamine-hydrolysing)
Identifiers
EC no. 6.3.5.5
CAS no. 37233-48-0
Databases
IntEnz IntEnz view
BRENDA BRENDA entry
ExPASy NiceZyme view
KEGG KEGG entry
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Search
PMC articles
PubMed articles
NCBI proteins
carbamoyl-phosphate synthetase 1, aspartate transcarbamylase, and dihydroorotase
Identifiers
SymbolCAD
NCBI gene 790
HGNC 1424
OMIM 114010
RefSeq NM_004341
UniProt P27708
Other data
Locus Chr. 2 p21
Search for
Structures Swiss-model
Domains InterPro

Carbamoyl phosphate synthetase (glutamine-hydrolysing) ( EC 6.3.5.5) is an enzyme that catalyzes the reactions that produce carbamoyl phosphate in the cytosol (as opposed to type I, which functions in the mitochondria). Its systemic name is hydrogen-carbonate:L-glutamine amido-ligase (ADP-forming, carbamate-phosphorylating). [1] [2] [3] [4] [5] [6] [7] [8]

In pyrimidine biosynthesis, it serves as the rate-limiting enzyme and catalyzes the following reaction:

2 ATP + L- glutamine + HCO3 + H2O 2 ADP + phosphate + L- glutamate + carbamoyl phosphate (overall reaction)
(1a) L-glutamine + H2O L-glutamate + NH3
(1b) 2 ATP + HCO3 + NH3 2 ADP + phosphate + carbamoyl phosphate

It is activated by ATP and PRPP [9] and it is inhibited by UTP (Uridine triphosphate) [10] Neither CPSI nor CPSII require biotin as a coenzyme, as seen with most carboxylation reactions.

It is one of the three enzyme functions coded by the CAD gene. It is classified under EC 6.3.5.5.

See also

References

  1. ^ Anderson PM, Meister A (December 1965). "Evidence for an activated form of carbon dioxide in the reaction catalyzed by Escherichia coli carbamyl phosphate synthetase". Biochemistry. 4 (12): 2803–9. doi: 10.1021/bi00888a034. PMID  5326356.
  2. ^ Kalman SM, Duffield PH, Brzozowski T (April 1966). "Purification and properties of a bacterial carbamyl phosphate synthetase". The Journal of Biological Chemistry. 241 (8): 1871–7. doi: 10.1016/S0021-9258(18)96716-5. PMID  5329589.
  3. ^ Yip MC, Knox WE (May 1970). "Glutamine-dependent carbamyl phosphate synthetase. Properties and distribution in normal and neoplastic rat tissues". The Journal of Biological Chemistry. 245 (9): 2199–204. doi: 10.1016/S0021-9258(18)63139-4. PMID  5442268.
  4. ^ Stapleton MA, Javid-Majd F, Harmon MF, Hanks BA, Grahmann JL, Mullins LS, Raushel FM (November 1996). "Role of conserved residues within the carboxy phosphate domain of carbamoyl phosphate synthetase". Biochemistry. 35 (45): 14352–61. doi: 10.1021/bi961183y. PMID  8916922.
  5. ^ Holden HM, Thoden JB, Raushel FM (December 1998). "Carbamoyl phosphate synthetase: a tunnel runs through it". Current Opinion in Structural Biology. 8 (6): 679–85. doi: 10.1016/s0959-440x(98)80086-9. PMID  9914247.
  6. ^ Raushel FM, Thoden JB, Reinhart GD, Holden HM (October 1998). "Carbamoyl phosphate synthetase: a crooked path from substrates to products". Current Opinion in Chemical Biology. 2 (5): 624–32. doi: 10.1016/s1367-5931(98)80094-x. PMID  9818189.
  7. ^ Raushel FM, Thoden JB, Holden HM (June 1999). "The amidotransferase family of enzymes: molecular machines for the production and delivery of ammonia". Biochemistry. 38 (25): 7891–9. doi: 10.1021/bi990871p. PMID  10387030.
  8. ^ Thoden JB, Huang X, Raushel FM, Holden HM (October 2002). "Carbamoyl-phosphate synthetase. Creation of an escape route for ammonia". The Journal of Biological Chemistry. 277 (42): 39722–7. doi: 10.1074/jbc.M206915200. PMID  12130656.
  9. ^ Inkling. "Unsupported Browser". Inkling. Retrieved 25 April 2018.
  10. ^ Engelking LR. Pyrimidine biosynthesis. Textbook of Veterinary Physiological Chemistry. 2015;:83–7. https://doi.org/10.1016/B978-0-12-391909-0.50014-1 Retrieved 1 April 2023

External links



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