Target type: biologicalprocess
The transfer of electrons through a series of electron donors and acceptors, generating energy that is ultimately used for synthesis of ATP. [ISBN:0716731363]
ATP synthesis coupled electron transport, also known as oxidative phosphorylation, is a fundamental biological process that generates the majority of ATP, the primary energy currency of cells. It occurs in the mitochondria, specifically in the inner mitochondrial membrane. The process involves a series of electron transfers down an electron transport chain, releasing energy used to pump protons across the membrane, creating a proton gradient. This gradient drives the synthesis of ATP by the enzyme ATP synthase. Here's a detailed breakdown:
1. **Electron Transport Chain:** The chain consists of four protein complexes (I, II, III, and IV) embedded in the inner mitochondrial membrane. Electrons from NADH and FADH2, generated from the breakdown of carbohydrates, fats, and proteins, enter the chain at different points. As electrons move down the chain, they lose energy, which is used to pump protons from the mitochondrial matrix to the intermembrane space.
2. **Proton Gradient:** The pumping of protons creates a proton gradient across the inner mitochondrial membrane. The concentration of protons is higher in the intermembrane space than in the matrix. This gradient represents potential energy, like a dam holding back water.
3. **ATP Synthase:** ATP synthase is a complex enzyme that spans the inner mitochondrial membrane. It has two main components: F0 and F1. F0 forms a channel through which protons flow back into the matrix, driven by the proton gradient. This flow of protons rotates the F1 component, which acts like a motor to drive the synthesis of ATP from ADP and inorganic phosphate.
4. **ATP Synthesis:** The rotation of F1 causes conformational changes in the enzyme, allowing it to bind ADP and phosphate, and then catalyze their reaction to form ATP. This process is highly efficient, producing approximately 3 ATP molecules for every pair of electrons that pass through the chain.
In summary, ATP synthesis coupled electron transport is a complex but elegant process that harnesses the energy from electron transfers to create a proton gradient, which in turn drives the synthesis of ATP. This process is essential for all living organisms, providing the energy required for all cellular activities.'
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Protein | Definition | Taxonomy |
---|---|---|
Cytochrome c oxidase subunit 2 | A cytochrome c oxidase subunit 2 that is encoded in the genome of human. [PRO:CNA, UniProtKB:P00403] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
celecoxib | organofluorine compound; pyrazoles; sulfonamide; toluenes | cyclooxygenase 2 inhibitor; geroprotector; non-narcotic analgesic; non-steroidal anti-inflammatory drug | |
diclofenac | diclofenac : A monocarboxylic acid consisting of phenylacetic acid having a (2,6-dichlorophenyl)amino group at the 2-position. Diclofenac: A non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt. | amino acid; aromatic amine; dichlorobenzene; monocarboxylic acid; secondary amino compound | antipyretic; drug allergen; EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor; environmental contaminant; non-narcotic analgesic; non-steroidal anti-inflammatory drug; xenobiotic |
flufenamic acid | flufenamic acid : An aromatic amino acid consisting of anthranilic acid carrying an N-(trifluoromethyl)phenyl substituent. An analgesic and anti-inflammatory, it is used in rheumatic disorders. Flufenamic Acid: An anthranilic acid derivative with analgesic, anti-inflammatory, and antipyretic properties. It is used in musculoskeletal and joint disorders and administered by mouth and topically. (From Martindale, The Extra Pharmacopoeia, 30th ed, p16) | aromatic amino acid; organofluorine compound | antipyretic; EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor; non-narcotic analgesic; non-steroidal anti-inflammatory drug |
indomethacin | indometacin : A member of the class of indole-3-acetic acids that is indole-3-acetic acid in which the indole ring is substituted at positions 1, 2 and 5 by p-chlorobenzoyl, methyl, and methoxy groups, respectively. A non-steroidal anti-inflammatory drug, it is used in the treatment of musculoskeletal and joint disorders including osteoarthritis, rheumatoid arthritis, gout, bursitis and tendinitis. Indomethacin: A non-steroidal anti-inflammatory agent (NSAID) that inhibits CYCLOOXYGENASE, which is necessary for the formation of PROSTAGLANDINS and other AUTACOIDS. It also inhibits the motility of POLYMORPHONUCLEAR LEUKOCYTES. | aromatic ether; indole-3-acetic acids; monochlorobenzenes; N-acylindole | analgesic; drug metabolite; EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor; environmental contaminant; gout suppressant; non-steroidal anti-inflammatory drug; xenobiotic; xenobiotic metabolite |
rofecoxib | butenolide; sulfone | analgesic; cyclooxygenase 2 inhibitor; non-steroidal anti-inflammatory drug | |
valdecoxib | isoxazoles; sulfonamide | antipyretic; antirheumatic drug; cyclooxygenase 2 inhibitor; non-narcotic analgesic; non-steroidal anti-inflammatory drug | |
tolfenamic acid | tolfenamic acid : An aminobenzoic acid that is anthranilic acid in which one of the hydrogens attached to the nitrogen is replaced by a 3-chloro-2-methylphenyl group. Tolfenamic acid is used specifically for relieving the pain of migraine. It also shows anticancer activity. tolfenamic acid: structure | aminobenzoic acid; organochlorine compound; secondary amino compound | EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor; EC 2.7.1.33 (pantothenate kinase) inhibitor; non-narcotic analgesic; non-steroidal anti-inflammatory drug |