| Record Information | 
|---|
| Version | 1.0 | 
|---|
| Update Date | 1/22/2018 12:54:54 PM | 
|---|
| Metabolite ID | PAMDB004054 | 
|---|
| Identification | 
|---|
| Name: | PG(12:0/12:0(3-OH)) | 
|---|
| Description: | PG(12:0/12:0(3-OH)) 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(12:0/12:0(3-OH)), in particular, consists of one dodecanoyl chain  to the C-1 atom, and one 3-hydroxydodecanoyl  to the C-2 atom. In Pseudomonas aeruginosa 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: | 1-dodecanoyl-2-3-hydroxydodecanoyl-sn-glycero-3-phospho-(1'-glycerol)1-dodecanoyl-2-3-hydroxydodecanoyl-sn-glycero-3-phosphoglycerol1-dodecanoyl-2-3-hydroxydodecanoyl-sn-glycero-3-phosphoglycerolGPG(12:0/12:0)GPG(24:0)PG(12:0/12:0)PG(24:0)Phosphatidylglycerol(12:0/12:0)Phosphatidylglycerol(24:0)
 | 
|---|
| Chemical Formula: | C30H59O11P | 
|---|
| Average Molecular Weight: | 626.765 | 
|---|
| Monoisotopic Molecular 
		Weight: | 626.379499718 | 
|---|
| InChI Key: | FMVLSWAYCHIRMK-GUQXXGRISA-N | 
|---|
| InChI: | InChI=1S/C30H59O11P/c1-3-5-7-9-11-12-14-16-18-20-29(34)41-28(25-40-42(36,37)39-23-27(33)22-31)24-38-30(35)21-26(32)19-17-15-13-10-8-6-4-2/h26-28,31-33H,3-25H2,1-2H3,(H,36,37)/t26?,27-,28+/m0/s1 | 
|---|
| CAS 
	number: | Not Available | 
|---|
| IUPAC Name: | [(2S)-2,3-dihydroxypropoxy][(2R)-2-(dodecanoyloxy)-3-[(3-hydroxydodecanoyl)oxy]propoxy]phosphinic acid | 
|---|
| Traditional IUPAC Name: | (2S)-2,3-dihydroxypropoxy((2R)-2-(dodecanoyloxy)-3-[(3-hydroxydodecanoyl)oxy]propoxy)phosphinic acid | 
|---|
| SMILES: | [H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CC(O)CCCCCCCCC)OC(=O)CCCCCCCCCCC | 
|---|
| Chemical Taxonomy | 
|---|
| Taxonomy Description | This compound belongs to the class of organic compounds known as phosphatidylglycerols. These are glycerophosphoglycerols in which two fatty acids are bonded to the 1-glycerol moiety through ester linkages. | 
|---|
| Kingdom | Organic compounds | 
|---|
| Super Class | Lipids and lipid-like molecules | 
|---|
| Class | Glycerophospholipids | 
|---|
| Sub Class | Glycerophosphoglycerols | 
|---|
| Direct Parent | Phosphatidylglycerols | 
|---|
| Alternative Parents |  | 
|---|
| Substituents | 1,2-diacylglycerophosphoglycerolBeta-hydroxy acidDialkyl phosphateFatty acid esterFatty acylAlkyl phosphateDicarboxylic acid or derivativesPhosphoric acid esterOrganic phosphoric acid derivativeHydroxy acid1,2-diolCarboxylic acid esterSecondary alcoholCarboxylic acid derivativePrimary alcoholHydrocarbon derivativeOrganic oxygen compoundCarbonyl groupOrganic oxideAlcoholOrganooxygen compoundAliphatic acyclic compound
 | 
|---|
| Molecular Framework | Aliphatic acyclic compounds | 
|---|
| External Descriptors | Not Available | 
|---|
| Physical Properties | 
|---|
| State: | Solid | 
|---|
| Charge: | -1 | 
|---|
| Melting point: | Not Available | 
|---|
| Experimental Properties: |  | 
|---|
| Predicted Properties |  | 
|---|
| Biological Properties | 
|---|
| Cellular Locations: | Membrane | 
|---|
| Reactions: |   | 
|---|
| Pathways: |  | 
|---|
| Spectra | 
|---|
| Spectra: |  | 
|---|
| References | 
|---|
| References: | Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., Tanabe, M. (2012). "KEGG for integration and interpretation of large-scale molecular data sets." Nucleic Acids Res 40:D109-D114. Pubmed: 22080510 Taylor SS, Heath EC. (1969) "The incorporation of beta-hydroxy fatty acids into a phospholipid of Escherichia coli B."  J Biol Chem. 244(24):6605-16. Pubmed: 4902888 Yurtsever D. (2007). Fatty acid methyl ester profiling of Enterococcus and Esherichia coli for microbial source tracking. M.sc. Thesis. Villanova University: U.S.A
 | 
|---|
| Synthesis Reference: | Not Available | 
|---|
| Material Safety Data Sheet (MSDS) | Not Available | 
|---|
| Links | 
|---|
| External Links: | | Resource | Link | 
|---|
 | CHEBI ID | Not Available |  | HMDB ID | Not Available |  | Pubchem Compound ID | Not Available |  | Kegg ID | Not Available |  | ChemSpider ID | Not Available |  | Wikipedia ID | Not Available |  | BioCyc ID | Not Available | 
 | 
|---|