Target type: biologicalprocess
The transfer of electrons from cytochrome c to oxygen that occurs during oxidative phosphorylation, mediated by the multisubunit enzyme known as complex IV. [ISBN:0716731363]
Mitochondrial electron transport from cytochrome c to oxygen is the final stage of cellular respiration, where electrons are transferred from cytochrome c to molecular oxygen, generating a proton gradient that drives ATP synthesis. This process occurs in the inner mitochondrial membrane, specifically within the electron transport chain (ETC).
The ETC consists of four major protein complexes: Complex III (cytochrome bc1 complex), Complex IV (cytochrome c oxidase), and two mobile electron carriers, cytochrome c and ubiquinone (CoQ).
1. Cytochrome c, a small, soluble protein, carries electrons from Complex III to Complex IV. Cytochrome c contains a heme group that can reversibly bind and release electrons.
2. Complex IV, also known as cytochrome c oxidase, is a large protein complex embedded in the inner mitochondrial membrane. It contains two heme groups (a and a3) and two copper ions (CuA and CuB). Complex IV accepts electrons from cytochrome c and uses them to reduce molecular oxygen (O2) to water (H2O).
3. The reduction of oxygen to water is a four-electron process that occurs in a series of steps:
a. The first step involves the binding of oxygen to the heme a3 and CuB centers of Complex IV.
b. Electrons from cytochrome c are transferred to the heme a3 and CuB centers, reducing oxygen to a superoxide anion (O2-).
c. Two more electrons are transferred, reducing the superoxide anion to hydrogen peroxide (H2O2).
d. The final two electrons are transferred, reducing hydrogen peroxide to water.
4. During the electron transfer process, protons (H+) are pumped from the mitochondrial matrix across the inner mitochondrial membrane and into the intermembrane space. This creates a proton gradient, a difference in proton concentration between the two compartments.
5. The proton gradient represents a form of potential energy that can be used to generate ATP. ATP synthase, another protein complex embedded in the inner mitochondrial membrane, utilizes the proton gradient to drive the synthesis of ATP from ADP and inorganic phosphate (Pi).
The electron transport chain is a highly regulated process that is essential for life. It provides the energy needed for all cellular processes, including muscle contraction, nerve impulse transmission, and protein synthesis. Disruptions in electron transport can lead to a variety of diseases, including mitochondrial diseases, neurodegenerative diseases, and cancer.'
"
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) |
Cytochrome c oxidase subunit 1 | A cytochrome c oxidase subunit 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P00395] | Homo sapiens (human) |
Cytochrome c oxidase subunit NDUFA4 | A cytochrome c oxidase subunit NDUFA4 that is encoded in the genome of human. [PRO:DNx, UniProtKB:O00483] | 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 |
aurapten | aurapten: RN refers to (E)-isomer; structure given in first source auraptene : A member of the class of coumarins that is umbelliferone in which the phenolic hydrogen has been replaced by a geranyl group. Ii is isolated from several edible fruits and vegetables and exhibits a variety of therapeutic properties. | coumarins; monoterpenoid | antihypertensive agent; antineoplastic agent; antioxidant; apoptosis inducer; dopaminergic agent; EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor; gamma-secretase modulator; gastrointestinal drug; hepatoprotective agent; matrix metalloproteinase inhibitor; neuroprotective agent; plant metabolite; PPARalpha agonist; vulnerary |
marmin | marmin: structure in first source; RN given for (R-(E))-isomer |