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{{unreferenced|date=June 2010}} |
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{{chembox |
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{{chembox |
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| Watchedfields = changed |
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| verifiedrevid = 443836799 |
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| verifiedrevid = 443837963 |
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| ImageFile = Glucose 1-phosphate.svg |
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| ImageFile = Glucose 1-phosphate.svg |
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| ImageSize = 150px |
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| ImageSize = 150px |
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| ImageCaption = Anionic form of α-<small>D</small>-glucose 1-phosphate |
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| ImageFile2 = Cori ester.gif |
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| ImageFile2 =Cori_ester.png |
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| ImageSize2 = 150px |
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| ImageSize2 = 150px |
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| IUPACName = Glucose 1-phosphate |
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| ImageCaption2 = Neutral form of α-<small>D</small>-glucose 1-phosphate |
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| IUPACName = <small>D</small>-Glucopyranosyl dihydrogen phosphate |
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| OtherNames = |
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| SystematicName = (2''Ξ'',3''R'',4''S'',5''S'',6''R'')-3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl dihydrogen phosphate |
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| Section1 = {{Chembox Identifiers |
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| OtherNames = Cori ester |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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|Section1={{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 388311 |
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| ChemSpiderID = 388311 |
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| InChI = 1/C6H13O9P/c7-1-2-3(8)4(9)5(10)6(14-2)15-16(11,12)13/h2-10H,1H2,(H2,11,12,13)/t2-,3-,4+,5-,6?/m1/s1 |
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| InChI = 1/C6H13O9P/c7-1-2-3(8)4(9)5(10)6(14-2)15-16(11,12)13/h2-10H,1H2,(H2,11,12,13)/t2-,3-,4+,5-,6?/m1/s1 |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo_Ref = {{cascite|correct|CAS}} |
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| CASNo = 59-56-3 |
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| CASNo = 59-56-3 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| PubChem = 65533 |
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| UNII = CIX3U01VAU |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| PubChem = 65533 |
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| KEGG = C00103 |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEBI = 16077 |
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| ChEBI = 16077 |
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| SMILES = O=P(O)(OC1O((O)(O)1O)CO)O |
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| SMILES = O=P(O)(OC1O((O)(O)1O)CO)O |
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| MeSHName = glucose-1-phosphate |
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| MeSHName = glucose-1-phosphate |
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| Section2 = {{Chembox Properties |
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|Section2={{Chembox Properties |
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| C=6 | H=13 | O=9 | P=1 |
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| Formula = C6H13O9P |
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| MolarMass = 260.136 |
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| Appearance = |
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| Appearance = |
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| Density = |
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| Density = |
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| MeltingPt = |
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| Section3 = {{Chembox Hazards |
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|Section3={{Chembox Hazards |
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| Solubility = |
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| MainHazards = |
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| MainHazards = |
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| FlashPt = |
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| FlashPt = |
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| AutoignitionPt = |
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| Autoignition = |
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'''Glucose 1-phosphate''' (also called '''cori ester''') is a ] molecule with a ] group on the 1'-carbon. |
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'''Glucose 1-phosphate''' (also called '''Cori ester''') is a ] molecule with a ] group on the 1'-carbon. It can exist in either the α- or β-]ic form. |
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==Reactions== |
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==Reactions of α-glucose 1-phosphate== |
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===Catabolic=== |
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===Catabolic=== |
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In ], it is the direct product of the reaction in which ] cleaves off a ] of ] from a greater ] structure. |
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In ], it is the direct product of the reaction in which ] cleaves off a ] of ] from a greater ] structure. A deficiency of muscle glycogen phosphorylase is known as ] (McArdle Disease). |
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To be utilized in cellular catabolism it must first be converted to ] by the ] ] in a free equilibrium.<ref>{{Citation|last=Pelley|first=John W.|title=8 - Gluconeogenesis and Glycogen Metabolism|date=2012-01-01|url=http://www.sciencedirect.com/science/article/pii/B9780323074469000088|work=Elsevier's Integrated Review Biochemistry (Second Edition)|pages=67–73|editor-last=Pelley|editor-first=John W.|place=Philadelphia|publisher=W.B. Saunders|language=en|doi=10.1016/b978-0-323-07446-9.00008-8|isbn=978-0-323-07446-9|access-date=2020-12-16}}</ref><ref>{{Citation|last=Isselbacher|first=Kurt J.|title=Galactose-1-phosphate Uridyl Transferase|date=1965-01-01|url=http://www.sciencedirect.com/science/article/pii/B9780123956309501535|work=Methods of Enzymatic Analysis|pages=863–866|editor-last=Bergmeyer|editor-first=Hans-Ulrich|publisher=Academic Press|language=en|doi=10.1016/b978-0-12-395630-9.50153-5|isbn=978-0-12-395630-9|access-date=2020-12-16}}</ref><ref>{{Citation|last=Bergmeyer|first=Hans-Ulrich|title=d-Glucose-1-phosphate|date=1965-01-01|url=http://www.sciencedirect.com/science/article/pii/B9780123956309500244|work=Methods of Enzymatic Analysis|pages=131–133|editor-last=Bergmeyer|editor-first=Hans-Ulrich|publisher=Academic Press|language=en|doi=10.1016/b978-0-12-395630-9.50024-4|isbn=978-0-12-395630-9|access-date=2020-12-16|last2=Klotzsch|first2=Helmut}}</ref> One reason that cells form glucose 1-phosphate instead of glucose during glycogen breakdown is that the very polar phosphorylated glucose cannot leave the cell membrane and so is marked for intracellular catabolism. ] deficiency is known as ] type 14 (GSD XIV).<ref></ref> |
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To be utilized in cellular catabolism it must first be converted to ] by the ] ]. One reason that cells form glucose 1-phosphate instead of glucose during glycogen breakdown is that the very polar phosphorylated glucose cannot leave the cell membrane and so is marked for intracellular catabolism. |
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===Anabolic=== |
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===Anabolic=== |
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In ], free glucose 1-phosphate can also react with ] to form ], by using the enzyme ]. It can then return to the greater glycogen structure via ]. |
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In ], free glucose 1-phosphate can also react with ] to form ],<ref name=":0">{{Citation|last=Blanco|first=Antonio|title=Chapter 19 - Integration and Regulation of Metabolism|date=2017-01-01|url=http://www.sciencedirect.com/science/article/pii/B9780128035504000197|work=Medical Biochemistry|pages=425–445|editor-last=Blanco|editor-first=Antonio|publisher=Academic Press|language=en|doi=10.1016/b978-0-12-803550-4.00019-7|isbn=978-0-12-803550-4|access-date=2020-12-16|last2=Blanco|first2=Gustavo|editor2-last=Blanco|editor2-first=Gustavo}}</ref> by using the enzyme ]. It can then return to the greater glycogen structure via ].<ref name=":0" /> |
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==β-Glucose 1-phosphate== |
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β-Glucose 1-phosphate is found in some microbes. It is produced by inverting α-glucan phosphorylases including ], ] and ] and is then converted into ] by ]. |
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==See also== |
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==See also== |
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* ] |
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* ] |
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==References== |
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{{reflist}} |
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{{biochem-stub}} |
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{{Glycogenesis and glycogenolysis metabolic intermediates}} |
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{{Glycogenesis and glycogenolysis metabolic intermediates}} |
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{{Fructose and galactose metabolic intermediates}} |
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{{Fructose and galactose metabolic intermediates}} |
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