1,3-Bisphosphoglyceric acid
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| IUPAC name
Phosphono 2-hydroxy-3-phosphonooxypropanoate
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| Systematic IUPAC name
(2-Hydroxy-3-phosphonooxy-propanoyloxy)phosphonic acid | |
| Other names
1,3-Diphosphoglycerate; Glycerate-1,3-bisphosphate; Glycerate-1,3-biphosphate; 1,3-Biphosphoglycerate; 3-Phosphoglyceroyl phosphate; Glyceric acid-1,3-diphosphate
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3D model (JSmol)
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| Abbreviations | 1,3BPG; 1,3-BPG; PGAP |
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CompTox Dashboard (EPA)
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| Properties | |
Chemical formula
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C3H8O10P2 |
| Molar mass | 266.035 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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1,3-Bisphosphoglyceric acid (1,3-Bisphosphoglycerate or 1,3BPG) is a three-carbon organic molecule present in most, if not all, living organisms.[1][2][3] It primarily exists as a metabolic intermediate in both glycolysis during respiration and the Calvin cycle during photosynthesis. 1,3BPG is a transitional stage between glycerate 3-phosphate and glyceraldehyde 3-phosphate during the fixation/reduction of CO2. 1,3BPG is also a precursor to 2,3-bisphosphoglycerate which is formed in the Luebering–Rapoport shunt of glycolysis in red blood cells.[4]
- ^ Alberts, Bruce; Heald, Rebecca; Johnson, Alexander; Morgan, David; Raff, Martin; Roberts, Keith; Walter, Peter (2022). Molecular Biology of the Cell (7th ed.). New York: W. W. Norton & Company.
- ^ Germann, William J.; Stanfield, Cindy L. (2002). Principles of Human Physiology. San Francisco: Benjamin Cummings. ISBN 0-8053-6056-5.
- ^ Berg, Jeremy Mark; Tymoczko, John L.; Stryer, Lubert (2002). Biochemistry (5th ed.). New York: W. H. Freeman and Company. ISBN 0-7167-4684-0.
- ^ Cite error: The named reference
Rapoport1950was invoked but never defined (see the help page).