Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Phosphoenolpyruvate (2-phosphoenolpyruvate, PEP) is the carboxylic acid derived from the enol of pyruvate and phosphate. It exists as an anion. PEP is an important intermediate in biochemistry. It has the highest-energy phosphate bond found (−61.9 kJ/mol) in organisms, and is involved in glycolysis and gluconeogenesis. In plants, it is also involved in the biosynthesis of various aromatic compounds, and in carbon fixation; in bacteria, it is also used as the source of energy for the phosphotransferase system.[1][2]
^Berg, Jeremy M.; Tymoczko, Stryer (2002). Biochemistry (5th ed.). New York: W.H. Freeman and Company. ISBN 0-7167-3051-0.
^Nelson, D. L.; Cox, M. M. "Lehninger, Principles of Biochemistry" 3rd Ed. Worth Publishing: New York, 2000. ISBN 1-57259-153-6.
and 8 Related for: Phosphoenolpyruvic acid information
Phosphoenolpyruvate (2-phosphoenolpyruvate, PEP) is the carboxylic acid derived from the enol of pyruvate and phosphate. It exists as an anion. PEP is...
restricted to the mitochondrion, and the enzymes that convert Phosphoenolpyruvicacid (PEP) to glucose-6-phosphate are found in the cytosol. The location...
converted into phosphoenolpyruvicacid (as C. jejuni lacks this synthetase), the pyruvate can enter the TCA cycle to form oxaloacetic acid intermediates...
carboxykinase) is responsible for converting oxaloacetate into phosphoenolpyruvicacid, or PEP, when guanosine triphosphate, GTP, is present. This step...
complication after endoscopic retrograde cholangiopancreatography Phosphoenolpyruvicacid, a biochemical compound Pep reaction, proton–electron–proton reaction...
accumulation of too much acid. Finally, PFK1 is allosterically inhibited by PEP, citrate, and ATP. Phosphoenolpyruvicacid is a product further downstream...
materials Phosphoenolpyruvicacid (PEP) and Erythrose 4-phosphate to form shikimic acid, which then further reacts to form specific aromatic amino acids. L-phenylalanine...
evolution are dedicated to amino acid biosynthesis. 21.3% of its protein-coding genes are dedicated to creating amino acids, while another 33% is dedicated...
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