Search results
Results from the WOW.Com Content Network
The overall process of oxidizing glucose to carbon dioxide, the combination of pathways 1 and 2, known as cellular respiration, produces about 30 equivalents of ATP from each molecule of glucose. [20] ATP production by a non-photosynthetic aerobic eukaryote occurs mainly in the mitochondria, which comprise nearly 25% of the volume of a typical ...
According to some newer sources, the ATP yield during aerobic respiration is not 36–38, but only about 30–32 ATP molecules / 1 molecule of glucose [17], because: ATP : NADH+H + and ATP : FADH 2 ratios during the oxidative phosphorylation appear to be not 3 and 2, but 2.5 and 1.5 respectively.
The above reactions are balanced if P i represents the H 2 PO 4 − ion, ADP and GDP the ADP 2− and GDP 2− ions, respectively, and ATP and GTP the ATP 3− and GTP 3− ions, respectively. The total number of ATP molecules obtained after complete oxidation of one glucose in glycolysis, citric acid cycle, and oxidative phosphorylation is ...
This gradient is used by the F O F 1 ATP synthase complex to make ATP via oxidative phosphorylation. ATP synthase is sometimes described as Complex V of the electron transport chain. [10] The F O component of ATP synthase acts as an ion channel that provides for a proton flux back into the mitochondrial matrix. It is composed of a, b and c ...
ATP synthase is an enzyme that catalyzes the formation of the energy storage molecule adenosine triphosphate (ATP) using adenosine diphosphate (ADP) and inorganic phosphate (P i). ATP synthase is a molecular machine. The overall reaction catalyzed by ATP synthase is: ADP + P i + 2H + out ⇌ ATP + H 2 O + 2H + in
Glycolysis produces only 2 ATP molecules, but somewhere between 30 and 36 ATPs are produced by the oxidative phosphorylation of the 10 NADH and 2 succinate molecules made by converting one molecule of glucose to carbon dioxide and water, [6] while each cycle of beta oxidation of a fatty acid yields about 14 ATPs. These ATP yields are ...
This Mg 2+ ion also coordinates with the terminal aspartate residue in the Walker B motif through the attacking H 2 O. [33] [34] [39] A general base, which may be the glutamate residue adjacent to the Walker B motif, [31] [40] [46] glutamine in the Q-loop, [30] [36] [40] or a histidine in the switch region that forms a hydrogen bond with the γ ...
The alpha/A and beta/B subunits can each be divided into three regions, or domains, centred on the ATP-binding pocket, and based on structure and function. The central domain contains the nucleotide-binding residues that make direct contact with the ADP/ATP molecule. [8]