mitochondrial phosphorylation - definição. O que é mitochondrial phosphorylation. Significado, conceito
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O que (quem) é mitochondrial phosphorylation - definição

PHOSPHORYLATION OF ADP TO ATP THAT ACCOMPANIES THE OXIDATION OF A METABOLITE THROUGH THE OPERATION OF THE RESPIRATORY CHAIN
Oxidative phosphorylation coupling factors; Oxidative phosphorylization; Oxidative phosporylation; Ox phos; Oxphos; Oxydative phosphorylation; ATP generation; Oxidative phosphorilation; Ox-phos; Mitochondrial oxidative phosphorylation; Mitochondrial β-oxidation; OXPHOS
  • Mechanism of [[ATP synthase]]. ATP is shown in red, ADP and phosphate in pink and the rotating γ subunit in black.
  • date=December 2022}}
  • Succinate-Q oxidoreductase]].
  • Q-cytochrome c oxidoreductase]]. After each step, Q (in the upper part of the figure) leaves the enzyme.
  • Complex IV: [[cytochrome c oxidase]].
  • cell]] is the site of oxidative phosphorylation. The NADH and succinate generated in the [[citric acid cycle]] are oxidized, releasing the energy of O<sub>2</sub> to power the [[ATP synthase]].
  • Reduction of [[coenzyme Q]] from its [[ubiquinone]] form (Q) to the reduced ubiquinol form (QH<sub>2</sub>).

Oxidative phosphorylation         
Oxidative phosphorylation (UK , US ) or electron transport-linked phosphorylation or terminal oxidation is the metabolic pathway in which cells use enzymes to oxidize nutrients, thereby releasing chemical energy in order to produce adenosine triphosphate (ATP). In eukaryotes, this takes place inside mitochondria.
Mitochondrial disease         
  • Example of a pedigree for a genetic trait inherited by mitochondrial DNA in animals and humans. Offspring of the males with the trait don't inherit the trait. Offspring of the females with the trait always inherit the trait (independently from their own gender).
SPONTANEOUSLY OCCURING OR INHERITED DISORDER THAT INVOLVES MITOCHONDRIAL DYSFUNCTION
Mitochondrial Diseases; Mitochondrial disorder; Mitochondrial diseases; Mitochondrial encephalomyopathies; Mitochondrial cytopathies; Disorders of mitochondrial metabolism; Dysautonomic mitochondrial myopathy; Mitochondriopathy; Mitochondrial disorders; Mitochondrial cytopathy; Ragged red fibres; Mitochondrial replacement; Mitochondrial DNA Mutations; Mitochondrial DNA mutations; Mitochondrial DNA mutation; Mitochondrial dysfunction; Mitochondria disease
Mitochondrial disease is a group of disorders caused by mitochondrial dysfunction. Mitochondria are the organelles that generate energy for the cell and are found in every cell of the human body except red blood cells.
Tyrosine phosphorylation         
  • right
THE PHOSPHORYLATION OF PEPTIDYL-TYROSINE TO FORM PEPTIDYL-O4'-PHOSPHO-L-TYROSINE.
Tyrosine-phosphorylation
Tyrosine phosphorylation is the addition of a phosphate (PO43−) group to the amino acid tyrosine on a protein. It is one of the main types of protein phosphorylation.

Wikipédia

Oxidative phosphorylation

Oxidative phosphorylation (UK , US ) or electron transport-linked phosphorylation or terminal oxidation is the metabolic pathway in which cells use enzymes to oxidize nutrients, thereby releasing chemical energy in order to produce adenosine triphosphate (ATP). In eukaryotes, this takes place inside mitochondria. Almost all aerobic organisms carry out oxidative phosphorylation. This pathway is so pervasive because it releases more energy than alternative fermentation processes such as anaerobic glycolysis.

The energy stored in the chemical bonds of glucose is released by the cell in the citric acid cycle producing carbon dioxide, and the energetic electron donors NADH and FADH. Oxidative phosphorylation uses these molecules and O2 to produce ATP, which is used throughout the cell whenever energy is needed. During oxidative phosphorylation, electrons are transferred from the electron donors to a series of electron acceptors in a series of redox reactions ending in oxygen, whose reaction releases half of the total energy.

In eukaryotes, these redox reactions are catalyzed by a series of protein complexes within the inner membrane of the cell's mitochondria, whereas, in prokaryotes, these proteins are located in the cell's outer membrane. These linked sets of proteins are called the electron transport chain. In eukaryotes, five main protein complexes are involved, whereas in prokaryotes many different enzymes are present, using a variety of electron donors and acceptors.

The energy transferred by electrons flowing through this electron transport chain is used to transport protons across the inner mitochondrial membrane, in a process called electron transport. This generates potential energy in the form of a pH gradient and an electrical potential across this membrane. This store of energy is tapped when protons flow back across the membrane and down the potential energy gradient, through a large enzyme called ATP synthase in a process called chemiosmosis. The ATP synthase uses the energy to transform adenosine diphosphate (ADP) into adenosine triphosphate, in a phosphorylation reaction. The reaction is driven by the proton flow, which forces the rotation of a part of the enzyme. The ATP synthase is a rotary mechanical motor.

Although oxidative phosphorylation is a vital part of metabolism, it produces reactive oxygen species such as superoxide and hydrogen peroxide, which lead to propagation of free radicals, damaging cells and contributing to disease and, possibly, aging and senescence. The enzymes carrying out this metabolic pathway are also the target of many drugs and poisons that inhibit their activities.