CAD protein


CAD protein is a trifunctional multi-domain enzyme involved in the first three steps of pyrimidine biosynthesis. De-novo synthesis starts with cytosolic carbamoylphosphate synthetase II which uses glutamine, carbon dioxide and ATP. This enzyme is inhibited by uridine triphosphate.
In 2015, the first observed pathological mutations of CAD were found in a four-year-old boy.
CAD protein has been observed in the mid-piece of mammalian spermatozoa, among the mitochondria.

Structure

CAD protein has a molecular weight of 243 KDa. It is a polypeptide made up of four different domains which make for a multi enzyme unit: Glutaminase, carbamoyl phosphate synthetase, Dihydroorotase and aspartate transcarbamoylase. The protein assembles into ~1.5MDa hexamers. More specifically, the DHO domain assembles into dimers, and ATC domains do so into trimers. The hexamers are then formed by DHO dimerization of two ATC trimers, and this connection does not impact the kinetic properties. In addition, it is thought that three GLN-CPS II dimers border the DHO-ATC complex. This is suggested by the fact that CPS II is not stable unless a part of the complex. DHO and ATC and are thought to be the main part of the formation of the protein. The active site is covered by a carboxylated lysine, serving as a bridge for two zinc ions. Another zinc ion helps stabilize a histidinate ion. The zinc and lysine are involved in the activity of the enzyme.

Function

This protein starts and controls the creation of pyrimidines in animals by acting as an enzyme. CAD is known to perform multiple reactions. For example, GLN and CPS II create carbamoyl phosphate from bicarbonate, glutamine, and two ATP molecules. The ATC then takes the newly made carbamoyl phosphate and forms carbamoyl aspartate by reacting with aspartate. DHO then takes carbamoyl aspartate and converts it to dihydroorotate. This molecule is a precursor of a pyrimidine ring, and this process shows the CAD protein's function in pyrimidine synthesis through carbamoyl-phosphate synthase and dihydroorotase activity.
In order to function, CAD requires certain co-factors. Zinc is needed for dihydroorotase activity, and thus three Zn+2 molecules bind to each subunit. Magnesium and manganese are also necessary, and either element is bound with four per subunit. The Michaelis-Menten constant, Km, shows the affinity of two molecules for one another. The Km of CAD for dihydroorotate is 28μM, and for N-carbamoyl-L-aspartate, it is 241μM.

Regulation

CAD protein is regulated by various molecules in order to increase or stop enzymatic activity. Uridine-5′-triphosphate is an end product that allosterically inhibits the CPS II step through negative feedback. Additionally, UMP acts as an allosteric inhibitor to the CPS II reaction. On the other hand, this step is activated by 5-phosphoribosyl-α-pyrophosphate, which is also a reactant for purine and pyrimidine synthesis. CAD activation can also occur by the addition of a phosphate group, done with S6 kinase, at the connection between DHO and ATC domains. CAD is also regulated in the mTOR pathway by mLST8, a protein that is part of the mTOR complex. More specifically, mTORC1 is a serine/threonine kinase that phosphorylates CAD, decreasing its activity.

Medical Implications

Congenital disorder of glycosylation, Type Iz is a rare disease caused by mutations in the CAD gene. This disease causes epileptic encephalopathy, normocytic anemia, anisopoikilocytosis, and a delay in childhood development. The disease is hereditary and autosomal recessive, and can be fatal in the early years of life.
There is also potential use for CAD protein as a target for treating certain tumors, as its role in pyrimidine synthesis can be manipulated to destroy cancer cells that are always growing and in need of new nucleotides. CAD can also be enhanced in order to increase certain types of cancer cells to chemotherapy. This has been shown to be specifically helpful in the treatment of Triple Negative Breast Cancer in vitro and in vivo.