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Nucleotide nucleotides Pyrimidine

A different, simpler , pathway is involved in the synthesis of pyrimidine nucleotides. A pyrimidine base (orotate), is synthesised first. Then the ribose is added from 5-phosphoribosyl 1-pyrophosphate. The two precursors for the formation of orotate are carbamoylphosphate and aspartate, which form carbamoyl aspartate, catalysed by aspartate carbamoyltransferase. [Pg.456]

Like purine nucleotides, pyrimidine nucleotides can be synthesized either de novo or by the salvage pathways from nucleobases or nucleosides. However, salvage is less efficient because, except in the case of utilization of uracil by bacteria, and to some extent by mammalian cells, pyrimidine nucleobases are not converted to nucleotides directly but only via nucleosides. [Pg.543]

In the following, any discussion of GG, XG, and GX sequences will imply that the neighboring nucleotides are pyrimidines which have no... [Pg.237]

Note N, any nucleotide Py, pyrimidine Pu, purine 1, site of single-strand cleavage (mirror image on complementary strand). [Pg.131]

The oligonucleotides in a pancreatic ribonuclease digest of RNA have the general formula (purine nucleotide) i pyrimidine nucleotide, n = 1, 2,3,... Thus for each value of the chain length, n nucleotides, the charge at neutral pH and the purine pyrimidine ratio are functions of n only and both increase monotonically with n. This... [Pg.280]

Pyrimidines Pyrimidine nucleotides (1) Pyrimidines (ii) Nucleotides derived from pyrimidines Meat... [Pg.146]

However, since the fate of the PRPP can be to form purine nucleotides, pyrimidine nucleotides, or coenzymes, the control must be complex and not limited to only purine nucleotides, pyrimidine nucleotides, or coenzymes. The next enzyme under control by purine nucleotides is PRPP transamidinase, catalyzing the formation of the phosphoribosyl amide (PRPP + glutamine PRNH2 + glutamate + pyrophosphate), the first unique precursor of purines. Since the synthesis ofPRPP is slow, there must be controls to allow its utilization in other processes when purine nucleotide pools are satisfied. The control of this system is interesting and shows the phenomena of synergism. That is, AMP, the product of one branch of the pathway, can inhibit the enzyme activity approximately 10% GMP, the product of the other branch of the pathway, can also cause approximately a 10% inhibition. [Pg.543]

Notes 1. Abbreviations used are NMP, any monophosphate nucleotide, Py, pyrimidine base purine base. [Pg.426]

Polynucleotides are the group of natural polymers in which the monomeric units are formed by a type of biomolecule known as nucleotides. Nucleotides are basically nucleoside phosphates. Nucleoside is the part of a nucleotide that is formed by glycosidic linkage between a monosaccharide and a type of nitrogenous compound called a nucleotide base. The nucleotide base may be of two types a purine base or a pyrimidine base. Depending... [Pg.30]

Hereditary deficiency of erythrocyte pyrimidine 5 nucleotidase results in a chronic haemolytic anaemia. The red cells show basophilic stippling and contain a markedly increased content of nucleotides, 3-6 times greater than normal, and 65 to 80% of nucleotides are pyrimidine in type (Valentine, et al., 1974 Torrance and Whittaker, 1979). Pyrimidine 5 nucleotidase is unique amongst the 5 nucleotidases in its strict substrate specificity for pyrimidine nucleoside 5 monophosphates, its pH profile, and for its cytosolic localisation (Paglia and Valentine, 1975). [Pg.103]

Torrance, J. D., and Whittaker, D., 1979, Distribution of erythrocyte nucleotides in pyrimidine 5 -nucleotidase deficiency, Brit. J. Haematol., 43 423. [Pg.108]

The specificity of ribonuclease has been studied with small synthetic substrates. When diesters of various nucleotides are subjected to RNAase, only those compounds that are derivatives of pyrimidine nucleoside 3 -phosphate are hydrolyzed purine nucleotides and pyrimidine 2 - or 5 -phosphates are resistant to this enzyme. With both model substrates and ribonucleic acid, the action of RNAase has been shown to include the intermediate formation of cyclic nucleotides (III). ... [Pg.256]

FIGURE 3 Generalized hairpin ribozyme. The target RNA (upper sequence) base pairs with the ribozyme (lower sequence) by Watson-Crick base-pairing. Cieavage occurs at the site indicated. The helices formed by the ribozyme and substrate are designated as H1-H4, as indicated. N = any nucleotide, Y=pyrimidine, P = purine. Other bases are A = adenosine, C = cytosine, G = guanosine, and U = uracil. [Pg.88]

This phenomenon has been studied particularly thoroughly by Marmur and co-workers, using phage SP8 for this purpose (Marmur and Greenspan, 1963 Marmur, Greenspan,etal,1963). Each of the two chains of this phage differ so much from the other in its nucleotide composition (pyrimidines are predominant in one chain, but purines in the complementary chain) that, after... [Pg.69]

Purine and pyrimidine bases Nucleosides Nucleotides Nucleic acids... [Pg.1155]

The primary stmcture of DNA is based on repeating nucleotide units, where each nucleotide is made up of the sugar, ie, 2 -deoxyribose, a phosphate, and a heterocycHc base, N. The most common DNA bases are the purines, adenine (A) and guanine (G), and the pyrimidines, thymine (T) and cytosine (C) (Fig. 1). The base, N, is bound at the I -position of the ribose unit through a heterocycHc nitrogen. [Pg.248]

Proteias are metabolized coatiauously by all living organisms, and are ia dyaamic equilibrium ia living cells (6,12). The role of amino acids ia proteia biosyathesis has beea described (2). Most of the amino acids absorbed through the digestioa of proteias are used to replace body proteias. The remaining portioa is metabolized iato various bioactive substances such as hormones and purine and pyrimidine nucleotides, (the precursors of DNA and RNA) or is consumed as an energy source (6,13). [Pg.271]

The pathways for thiamine biosynthesis have been elucidated only partiy. Thiamine pyrophosphate is made universally from the precursors 4-amino-5-hydroxymethyl-2-methylpytimidinepyrophosphate [841-01-0] (47) and 4-methyl-5-(2-hydroxyethyl)thiazolephosphate [3269-79-2] (48), but there appear to be different pathways ia the eadier steps. In bacteria, the early steps of the pyrimidine biosynthesis are same as those of purine nucleotide biosynthesis, 5-Aminoimidazole ribotide [41535-66-4] (AIR) (49) appears to be the sole and last common iatermediate ultimately the elements are suppHed by glycine, formate, and ribose. AIR is rearranged in a complex manner to the pyrimidine by an as-yet undetermined mechanism. In yeasts, the pathway to the pyrimidine is less well understood and maybe different (74—83) (Fig. 9). [Pg.92]


See other pages where Nucleotide nucleotides Pyrimidine is mentioned: [Pg.1050]    [Pg.93]    [Pg.94]    [Pg.375]    [Pg.124]    [Pg.1001]    [Pg.281]    [Pg.323]    [Pg.61]    [Pg.79]    [Pg.496]    [Pg.746]    [Pg.1050]    [Pg.480]    [Pg.443]    [Pg.31]    [Pg.208]    [Pg.260]    [Pg.263]    [Pg.270]    [Pg.174]    [Pg.259]    [Pg.188]    [Pg.283]    [Pg.284]    [Pg.1181]    [Pg.1188]    [Pg.117]   


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Biosynthesis of Pyrimidine Nucleotides

Catabolism of pyrimidine nucleotides

Coordination of Purine and Pyrimidine Nucleotide Biosynthesis

De novo pyrimidine nucleotide metabolism

Formation of Other Pyrimidine Nucleotides

Nucleotides Purine Pyrimidines

Nucleotides pyrimidine deoxy

Purine and pyrimidine nucleotide

Purine and pyrimidine nucleotide biosynthesis

Pyrimidine Nucleoside Bases, Purines, Nucleotides, Nucleosides, and Nucleic Acids

Pyrimidine Nucleotides and Nucleosides

Pyrimidine nucleotide chromatography

Pyrimidine nucleotide hydrolysis

Pyrimidine nucleotides

Pyrimidine nucleotides

Pyrimidine nucleotides Nucleotide , synthesis

Pyrimidine nucleotides analogues

Pyrimidine nucleotides catabolism

Pyrimidine nucleotides derivatives

Pyrimidine nucleotides formation

Pyrimidine nucleotides interconversion

Pyrimidine nucleotides synthesis

Pyrimidine nucleotides synthesis, PRPP precursor

Pyrimidine nucleotides, irradiation

Pyrimidine nucleotides,inhibition

Pyrimidine, aromaticity nucleotides from

Pyrimidines nucleotides, biosynthesis

Pyrimidines/pyrimidine nucleotides

Pyrimidines/pyrimidine nucleotides

Pyrimidines/pyrimidine nucleotides catalysts

Pyrimidines/pyrimidine nucleotides metabolism

Pyrimidines/pyrimidine nucleotides regulation

Pyrimidines/pyrimidine nucleotides synthesis

Pyrimidines/pyrimidine nucleotides ultraviolet light absorbed

Synthesis of Pyrimidine Nucleotides

The Anabolism of Pyrimidine Nucleotides

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