Showing metabocard for PG(10:0(3-OH)/12:0) (MMDBc0031427)
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| Version | 1.0 | ||||||||||||
| Status | Detected and Quantified | ||||||||||||
| Creation Date | 2021-11-18 00:48:36 UTC | ||||||||||||
| Update Date | 2022-08-31 18:10:35 UTC | ||||||||||||
| Metabolite ID | MMDBc0031427 | ||||||||||||
| Metabolite Identification | |||||||||||||
| Common Name | PG(10:0(3-OH)/12:0) | ||||||||||||
| Description | PG(10:0(3-OH)/12:0) is a phosphatidylglycerol. Phosphatidylglycerols consist of a glycerol 3-phosphate backbone esterified to either saturated or unsaturated fatty acids on carbons 1 and 2. As is the case with diacylglycerols, phosphatidylglycerols can have many different combinations of fatty acids of varying lengths and saturation attached to the C-1 and C-2 positions. PG(10:0(3-OH)/12:0), in particular, consists of one 3-hydroxydecanoyl chain to the C-1 atom, and one dodecanoyl to the C-2 atom. In E. coli glycerophospholipid metabolism, phosphatidylglycerol is formed from phosphatidic acid (1,2-diacyl-sn-glycerol 3-phosphate) by a sequence of enzymatic reactions that proceeds via two intermediates, cytidine diphosphate diacylglycerol (CDP-diacylglycerol) and phosphatidylglycerophosphate (PGP, a phosphorylated phosphatidylglycerol). Phosphatidylglycerols, along with CDP-diacylglycerol, also serve as precursor molecules for the synthesis of cardiolipin, a phospholipid found in membranes. | ||||||||||||
| Structure |  | ||||||||||||
| Synonyms | Not Available | ||||||||||||
| Molecular Formula | C28H55O11P | ||||||||||||
| Average Mass | 598.711 | ||||||||||||
| Monoisotopic Mass | 598.348199589 | ||||||||||||
| IUPAC Name | Not Available | ||||||||||||
| Traditional Name | Not Available | ||||||||||||
| CAS Registry Number | Not Available | ||||||||||||
| SMILES | Not Available | ||||||||||||
| InChI Identifier | InChI=1S/C28H55O11P/c1-3-5-7-9-10-11-12-14-16-18-27(32)36-22-26(23-38-40(34,35)37-21-25(31)20-29)39-28(33)19-24(30)17-15-13-8-6-4-2/h24-26,29-31H,3-23H2,1-2H3,(H,34,35)/t24?,25-,26+/m0/s1 | ||||||||||||
| InChI Key | WNBRGPQLLNLAIC-XBCLTQTASA-N | ||||||||||||
| Chemical Taxonomy | |||||||||||||
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| Physical Properties | |||||||||||||
| State | Solid | ||||||||||||
| Predicted Properties | Not Available | ||||||||||||
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| Retention Times | Not Available | ||||||||||||
| Retention Indices | Not Available | ||||||||||||
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| Retention Times | Not Available | ||||||||||||
| Retention Indices | Not Available | ||||||||||||
| Biological Properties | |||||||||||||
| Cellular Locations | Not Available | ||||||||||||
| Biospecimen Locations | Not Available | ||||||||||||
| Tissue Locations | Not Available | ||||||||||||
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| Pathways | Not Available | ||||||||||||
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Reactions This table shows at most 20 reactions. For the full list of associated reactions: See All Associated Reactions
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| External Links | |||||||||||||
| External Links | Not Available | ||||||||||||
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