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Adenosine cycle

Molybdate is also known as an inhibitor of the important enzyme ATP sulfurylase where ATP is adenosine triphosphate, which activates sulfate for participation in biosynthetic pathways (56). The tetrahedral molybdate dianion, MoO , substitutes for the tetrahedral sulfate dianion, SO , and leads to futile cycling of the enzyme and total inhibition of sulfate activation. Molybdate is also a co-effector in the receptor for steroids (qv) in mammalian systems, a biochemical finding that may also have physiological implications (57). [Pg.475]

Figure 29.1 An overview of catabolic pathways for the degradation of food and the production of biochemical energy. The ultimate products of food catabolism are C02 and H2O, with the energy released in the citric acid cycle used to drive the endergonic synthesis of adenosine triphosphate (ATP) from adenosine diphosphate (ADP) plus phosphate ion, HOPO32-. Figure 29.1 An overview of catabolic pathways for the degradation of food and the production of biochemical energy. The ultimate products of food catabolism are C02 and H2O, with the energy released in the citric acid cycle used to drive the endergonic synthesis of adenosine triphosphate (ATP) from adenosine diphosphate (ADP) plus phosphate ion, HOPO32-.
Phosphate also plays a central role in the transmission and control of chemical energy within the cells primarily via the hydrolysis of the terminal phosphate ester bond of the adenosine triphosphate (ATP) molecule (Fig. 14-3b). In addition, phosphate is a necessary constituent of phospholipids, which are important components in cell membranes, and as mentioned before, of apatite, which forms structural body parts such as teeth and bones. It is not surprising, therefore, that the cycling of P is closely linked with biological processes. This connection is, in fact, inseparable as organisms cannot exist without P, and their existence controls, to a large extent, the natural distribution of P. [Pg.363]

The ventricular action potential is depicted in Fig. 6-2.2 Myocyte resting membrane potential is usually -70 to -90 mV, due to the action of the sodium-potassium adenosine triphosphatase (ATPase) pump, which maintains relatively high extracellular sodium concentrations and relatively low extracellular potassium concentrations. During each action potential cycle, the potential of the membrane increases to a threshold potential, usually -60 to -80 mV. When the membrane potential reaches this threshold, the fast sodium channels open, allowing sodium ions to rapidly enter the cell. This rapid influx of positive ions... [Pg.109]

The effect of receptor stimulation is thus to catalyze a reaction cycle. This leads to considerable amplification of the initial signal. For example, in the process of visual excitation, the photoisomerization of one rhodopsin molecule leads to the activation of approximately 500 to 1000 transdudn (Gt) molecules, each of which in turn catalyzes the hydrolysis of many hundreds of cyclic guanosine monophosphate (cGMP) molecules by phosphodiesterase. Amplification in the adenylate cyclase cascade is less but still substantial each ligand-bound P-adrenoceptor activates approximately 10 to 20 Gs molecules, each of which in turn catalyzes the production of hundreds of cyclic adenosine monophosphate (cAMP) molecules by adenylate cyclase. [Pg.216]

Mitochondrial heterogeneity leads to multiple simultaneous TCA cycles in astrocytes and neurons 546 Partial TCA cycles can provide energy in brain 546 Adenosine triphosphate production in brain is highly regulated 546 Phosphocreatine has a role in maintaining adenosine triphosphate levels in brain 546... [Pg.532]

In the past decade, a large number of studies emphasized the heterogeneous scale-free degree distribution of metabolic networks Most substrates participate in only a few reactions, whereas a small number of metabolites ( hubs ) participate in a very large number of reactions [19,45,52]. Not surprisingly, the list of highly connected metabolites is headed by the ubiquitous cofactors, such as adenosine triphosphate (ATP), adenosine diphosphate (ADP), and nicotinamide adenine dinucleotide (NAD) in its various forms, as well as by intermediates of glycolysis and the tricarboxylic acid (TCA) cycle. [Pg.153]

Phosphate ion is a major participant in the biological energy cycle through the reactions of mono-, di-, and triphosphates, including one of the most important of these reactions, producing adenosine diphosphate from adenosine triphosphate (see structures in Section 2.3.1, Table 2.2) ... [Pg.192]

Figure 6.1 Pathways involved in glucose oxidation by plant cells (a) glycolysis, (b) Krebs cycle, (c) mitochondrial cytochrome chain. Under anoxic conditions. Reactions 1, 2 and 3 of glycolysis are catalysed by lactate dehydrogenase, pyruvate decarboxylase and alcohol dehydrogenase, respectively. ATP and ADP, adenosine tri- and diphosphate NAD and NADHa, oxidized and reduced forms of nicotinamide adenine dinucleotide PGA, phosphoglyceraldehyde PEP, phosphoenolpyruvate Acetyl-CoA, acetyl coenzyme A FP, flavoprotein cyt, cytochrome e, electron. (Modified from Fitter and Hay, 2002). Reprinted with permission from Elsevier... Figure 6.1 Pathways involved in glucose oxidation by plant cells (a) glycolysis, (b) Krebs cycle, (c) mitochondrial cytochrome chain. Under anoxic conditions. Reactions 1, 2 and 3 of glycolysis are catalysed by lactate dehydrogenase, pyruvate decarboxylase and alcohol dehydrogenase, respectively. ATP and ADP, adenosine tri- and diphosphate NAD and NADHa, oxidized and reduced forms of nicotinamide adenine dinucleotide PGA, phosphoglyceraldehyde PEP, phosphoenolpyruvate Acetyl-CoA, acetyl coenzyme A FP, flavoprotein cyt, cytochrome e, electron. (Modified from Fitter and Hay, 2002). Reprinted with permission from Elsevier...
The A-rich loop plays a role in retroviral replication and likely pairs with the complementary tRNA s anticodon. Strnctnral analysis of this A-rich loop shows a U-tum motif, an RNA strnctnre first seen in tRNA , but which is a common structural motif in many tRNAs." If, as evidence suggests, the four adenosines in the A-rich loop of the PBS pairing with the four uridines in the anticodon stem loop of tRNA y is a critical event in the HIV life cycle, this could provide a potential target for therapeutic intervention. [Pg.271]

Transfer of the methyl group from 5,-adenosylmethi-onine to an acceptor yields S -adenosylhomocysteine (Fig. 18-18, step (2)), which is subsequently broken down to homocysteine and adenosine (step (3)). Methionine is regenerated by transfer of a methyl group to homocysteine in a reaction catalyzed by methionine synthase (step (4)), and methionine is reconverted to 5-adenosyl-methionine to complete an activated-methyl cycle. [Pg.674]


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Futile cycle, between AMP and adenosine

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