Target type: biologicalprocess
The chemical reactions and pathways resulting in the formation of pyruvate, 2-oxopropanoate. [GOC:go_curators]
Pyruvate biosynthesis is a fundamental metabolic pathway in living organisms, crucial for generating pyruvate, a central molecule in cellular metabolism. This process serves as the final step in glycolysis, the breakdown of glucose to extract energy, and also contributes to other metabolic pathways like gluconeogenesis (glucose synthesis).
The process typically starts with phosphoenolpyruvate (PEP), a high-energy compound produced during glycolysis. PEP is converted to pyruvate through a series of enzymatic reactions:
1. **Phosphoenolpyruvate carboxykinase (PEPCK):** In some organisms, PEP is first decarboxylated by PEPCK, releasing carbon dioxide and forming oxaloacetate. This step is particularly important in gluconeogenesis, where pyruvate is generated from non-carbohydrate sources.
2. **Pyruvate kinase:** The key enzyme in pyruvate biosynthesis is pyruvate kinase, which catalyzes the transfer of a phosphate group from PEP to ADP, generating ATP and pyruvate. This reaction is irreversible under physiological conditions and plays a central role in energy production.
The resulting pyruvate can then enter various metabolic pathways depending on the organism's needs:
* **Aerobic conditions:** Pyruvate is transported into the mitochondria, where it is further oxidized in the citric acid cycle to generate energy in the form of ATP.
* **Anaerobic conditions:** In the absence of oxygen, pyruvate can be fermented into lactate or ethanol, regenerating NAD+ for glycolysis to continue.
* **Gluconeogenesis:** Pyruvate serves as a precursor for glucose synthesis during periods of fasting or low carbohydrate intake.
The pyruvate biosynthetic process is tightly regulated by various factors, including energy demand, nutrient availability, and hormonal signals. This intricate regulation ensures that the organism can efficiently generate and utilize pyruvate for its metabolic needs.'
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Protein | Definition | Taxonomy |
---|---|---|
Serine racemase | A serine racemase that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q9GZT4] | Homo sapiens (human) |
4-hydroxy-2-oxoglutarate aldolase, mitochondrial | A 4-hydroxy-2-oxoglutarate aldolase, mitochondrial that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q86XE5] | Homo sapiens (human) |
Pyruvate kinase PKLR | A pyruvate kinase PKLR that is encoded in the genome of human. [PRO:DNx, UniProtKB:P30613] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
benzoic acid | aromatic carboxylic acid : Any carboxylic acid in which the carboxy group is directly bonded to an aromatic ring. benzoic acid : A compound comprising a benzene ring core carrying a carboxylic acid substituent. Benzoic Acid: A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid. | benzoic acids | algal metabolite; antimicrobial food preservative; drug allergen; EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor; EC 3.1.1.3 (triacylglycerol lipase) inhibitor; human xenobiotic metabolite; plant metabolite |
glycine | alpha-amino acid; amino acid zwitterion; proteinogenic amino acid; serine family amino acid | EC 2.1.2.1 (glycine hydroxymethyltransferase) inhibitor; fundamental metabolite; hepatoprotective agent; micronutrient; neurotransmitter; NMDA receptor agonist; nutraceutical | |
malonic acid | dicarboxylic acid : Any carboxylic acid containing two carboxy groups. malonic acid : An alpha,omega-dicarboxylic acid in which the two carboxy groups are separated by a single methylene group. | alpha,omega-dicarboxylic acid | human metabolite |
thiophene-3-carboxylic acid | thiophene-3-carboxylic acid: structure in first source | ||
chelidamic acid | |||
dipicolinic acid | dipicolinic acid : A pyridinedicarboxylic acid carrying two carboxy groups at positions 2 and 6. | pyridinedicarboxylic acid | bacterial metabolite |
3-hydroxy-1-benzopyran-2-one | 3-hydroxycoumarin: Photoprotective from sea urchin gametes and embryonic cells; structure in first source hydroxycoumarin : Any coumarin carrying at least one hydroxy substituent. | hydroxycoumarin | |
tricarballylic acid | tricarballylic acid : A tricarboxylic acid that is glutaric acid in which one of the beta-hydrogens is substituted by a carboxy group. tricarballylic acid: RN given refers to parent cpd | tricarboxylic acid | |
shikonin | shikonin: a naphthazarin; has antineoplastic and angiogenesis inhibiting activities | hydroxy-1,4-naphthoquinone | |
crotonic acid | butenoic acid : Any C4, straight-chain fatty acid containing one double bond. crotonic acid : A but-2-enoic acid with a trans- double bond at C-2. It has been isolated from Daucus carota. crotonic acid: a stereospecific unsaturated carboxylic acid found in CROTON OIL | 2-butenoic acid | plant metabolite |
3-coumaric acid | 3-coumaric acid : A monohydroxycinnamic acid in which the hydroxy substituent is located at C-3 of the phenyl ring. 3-coumaric acid: RN given refers to cpd without isomeric designation in Chemline trans-3-coumaric acid : A 3-coumaric acid that is phenol substituted with trans-2-propenoic acid at position C-3. | 3-coumaric acid | |
alizarin red s | alizarin red S : An organic sodium salt having 3,4-dihydroxy-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate as the counterion. It is commonly used to stain embryo skeletons in cleared whole mounts, usually of small mammals. Alizarin Red S: RN given refers to parent cpd; structure | organic sodium salt; organosulfonate salt | histological dye |
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