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Browse our CPS1 Proteins (CPS1)

Full name:
Carbamoyl-Phosphate Synthase 1, Mitochondrial Proteins (CPS1)
On are 3 Carbamoyl-Phosphate Synthase 1, Mitochondrial (CPS1) Proteins from 2 different suppliers available. Additionally we are shipping CPS1 Antibodies (112) and CPS1 Kits (4) and many more products for this protein. A total of 121 CPS1 products are currently listed.
4732433M03Rik, cps, CPSASE1, D1Ucla3
list all proteins Gene Name GeneID UniProt
CPS1 1373 P31327
CPS1 227231 Q8C196
Rat CPS1 CPS1 497840 P07756

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CPS1 Proteins (CPS1) by Origin

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More Proteins for CPS1 Interaction Partners

Xenopus laevis Carbamoyl-Phosphate Synthase 1, Mitochondrial (CPS1) interaction partners

Human Carbamoyl-Phosphate Synthase 1, Mitochondrial (CPS1) interaction partners

  1. CPS1 knockdown reduced cell growth, decreased levels of metabolites associated with nucleic acid biosynthesis.

  2. These results may offer an increasing understand that CPS1 might have a function in differentiation.

  3. Molecular structure of CPS1 has been deciphered.

  4. CPS1 and CPS1IT1 may be potential prognostic indicators for patients with intrahepatic cholangiocarcinoma.

  5. CPS1 is involved in the urea cycle in weight maintenance.

  6. More HCC (show FAM126A Proteins) cells could be identified by the antibody cocktail for CPS1 and P-CK compared with a single antibody.

  7. characterized the only currently known recurrent CPS1 mutation, p.Val1013del found in eleven unrelated patients of Turkish descent; mutation p.V1013del inactivates CPS1 but does not render the enzyme grossly unstable or insoluble

  8. Overexpression of CPS1 is associated with rectal cancers.

  9. study examined patient characteristics, including genetic polymorphism, to identify risk factors associated with development of hyperammonemia during valproic acid-based therapy; found CPS1 4217C>A polymorphism may not be associated with development of hyperammonemia in Japanese population

  10. Findings support the disease-causing role of the mutations reported to affect the CPS1 deficiency, revealing a key role of the small CPS1 domain of unknown function (UFSD) for proper enzyme folding.

Mouse (Murine) Carbamoyl-Phosphate Synthase 1, Mitochondrial (CPS1) interaction partners

  1. these data suggest that AhR (show AHR Proteins) activation promotes CPS1 recruitment to DNA enhancer sites in the genome, resulting in a specific enzyme-independent post-translational modification of the linker histone H1 (show H1F0 Proteins) protein (H1K34hcit), pivotal in altering local chromatin structure and transcriptional activation.

  2. The results suggest that elevated isoaspartate and CPS-1, and reduced CA-III (show CA3 Proteins) levels could serve as biomarkers of hepatocellular injury.

  3. CPS1 becomes readily detectable upon hepatocyte apoptotic and necrotic death. Its abundance and short serum half-life suggest that it may be a useful prognostic biomarker in acute liver injury.

  4. Taken together with previous findings regarding CPS1 structure and function, homology modeling of mouse CPS1 suggested that nitration at Y1450 in an alpha-helix of allosteric domain prevents activation of CPS1 by its activator, N-acetyl-l-glutamate (show GRIN1 Proteins).

  5. Because ammonia generated during fasting is toxic, SIRT5 (show SIRT5 Proteins) protein might play a protective role by converting ammonia to non-toxic urea through deacetylation and activation of CPS1.

  6. Y-box binding protein-1 (show YBX1 Proteins) down-regulates expression of carbamoyl phosphate synthetase-I by suppressing CCAAT enhancer-binding protein-alpha (show CEBPA Proteins) function in mice.

  7. SIRT5 (show SIRT5 Proteins) deacetylates CPS1 and upregulates its activity

CPS1 Protein Profile

Protein Summary

The mitochondrial enzyme encoded by this gene catalyzes synthesis of carbamoyl phosphate from ammonia and bicarbonate. This reaction is the first committed step of the urea cycle, which is important in the removal of excess urea from cells. The encoded protein may also represent a core mitochondrial nucleoid protein. Three transcript variants encoding different isoforms have been found for this gene. The shortest isoform may not be localized to the mitochondrion. Mutations in this gene have been associated with carbamoyl phosphate synthetase deficiency, susceptibility to persistent pulmonary hypertension, and susceptibility to venoocclusive disease after bone marrow transplantation.

Alternative names and synonyms associated with CPS1

  • carbamoyl-phosphate synthase 1, mitochondrial (cps1)
  • carbamoyl-phosphate synthase 1, mitochondrial (CPS1)
  • carbamoyl-phosphate synthetase 1 (Cps1)
  • 4732433M03Rik protein
  • cps protein
  • CPSASE1 protein
  • D1Ucla3 protein

Protein level used designations for CPS1

carbamoyl-phosphate synthase [ammonia], mitochondrial , carbamoyl-phosphate synthetase III , carbamoyl-phosphate synthase 1, mitochondrial , carbamoyl-phosphate synthetase 1, mitochondrial , carbamoyl-phosphate synthase [ammonia], mitochondrial-like , carbamoyl-phosphate synthetase I , carbamoyl phosphate synthetase 1 , carbamyl phosphate synthetase 1 , carbamoylphosphate synthetase I , CPSase I , carbamyl phosphate synthetase I , carboamyl-phosphate synthetase 1

100136758 Oncorhynchus mykiss
100402602 Callithrix jacchus
488506 Canis lupus familiaris
510506 Bos taurus
738670 Pan troglodytes
100050116 Equus caballus
733340 Xenopus laevis
428994 Gallus gallus
1373 Homo sapiens
227231 Mus musculus
497840 Rattus norvegicus
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