PE-NMe(18:1(9Z)/18:1(9Z)) (BioDeep_00000031648)
human metabolite Endogenous
代谢物信息卡片
化学式: C42H80NO8P (757.562125)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CCCCCCCCC=CCCCCCCCC(=O)OCC(COP(=O)(O)OCCNC)OC(=O)CCCCCCCC=CCCCCCCCC
InChI: InChI=1S/C42H80NO8P/c1-4-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-41(44)48-38-40(39-50-52(46,47)49-37-36-43-3)51-42(45)35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-5-2/h18-21,40,43H,4-17,22-39H2,1-3H3,(H,46,47)/t40-/m1/s1
描述信息
PE-NMe(18:1(9Z)/18:1(9Z)) is a monomethylphosphatidylethanolamine. It is a glycerophospholipid, and is formed by sequential methylation of phosphatidylethanolamine as part of a mechanism for biosynthesis of phosphatidylcholine. Monomethylphosphatidylethanolamines are usually found at trace levels in animal or plant tissues. They can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. PE-NMe(18:1(9Z)/18:1(9Z)), in particular, consists of two 9Z-octadecenoyl chain at positions C-1 and C2. Fatty acids containing 16, 18 and 20 carbons are the most common. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling.
PE-NMe(18:1(9Z)/18:1(9Z)) is a monomethylphosphatidylethanolamine. It is a glycerophospholipid, and is formed by sequential methylation of phosphatidylethanolamine as part of a mechanism for biosynthesis of phosphatidylcholine. Monomethylphosphatidylethanolamines are usually found at trace levels in animal or plant tissues. They can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling. (Lipid Library, Lipid MAPS) [HMDB]
同义名列表
11 个代谢物同义名
[(2R)-2,3-bis[(9Z)-octadec-9-enoyloxy]propoxy][2-(methylamino)ethoxy]phosphinic acid; (2R)-2,3-bis[(9Z)-octadec-9-enoyloxy]propoxy(2-(methylamino)ethoxy)phosphinic acid; 1,2-Di-(9Z-octadecenoyl)-sn-glycero-3-phospho-N-methylethanolamine zwitterion; 1,2-di-(9Z-octadecenoyl)-sn-glycero-3-phospho-N-methylethanolamine; 1,2-Dioleoyl-sn-glycero-3-phosphoethanolamine-N-monomethyl; N-Methyl-1,2-dioleoyl-sn-glycero-3-phosphoethanolamine; 1,2-Dioleoyl-sn-glycero-3-phosphoethanolamine-N-methyl; N-Methyl-1,2-dioleoylphosphatidylethanolamine; PE-NMe(18:1(9Z)/18:1(9Z)); MMPE(18:1(9Z)/18:1(9Z)); 1,2-DOPE-me
数据库引用编号
6 个数据库交叉引用编号
- ChEBI: CHEBI:85962
- PubChem: 9547032
- HMDB: HMDB0010565
- foodb: FDB027715
- chemspider: 7825982
- CAS: 96687-23-9
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
8 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(8)
- Lysolipid Incorporation into ER PC(18:1(9Z)/18:1(9Z)):
Glycerophosphocholine + Water ⟶ Choline + Glycerol 3-phosphate + Hydrogen Ion
- Lysolipid incorporation into Mitochondria PC(18:1(9Z)/18:1(9Z)):
Adenosine triphosphate + LysoPC(18:1(9Z)) + Water ⟶ Adenosine diphosphate + LysoPC(18:1(9Z)) + Phosphate
- Phosphatidylcholine biosynthesis PC(18:1(9Z)/18:1(9Z)):
PE(18:1(9Z)/18:1(9Z)) + S-Adenosylmethionine ⟶ Hydrogen Ion + PE-NMe(18:1(9Z)/18:1(9Z)) + S-Adenosylhomocysteine
- Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:1(9Z)):
Adenosine triphosphate + Choline ⟶ Adenosine diphosphate + Phosphorylcholine
- Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:1(9Z)):
Hydrogen Ion + L-Serine ⟶ Carbon dioxide + Ethanolamine
- Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:1(9Z)):
Adenosine triphosphate + Choline ⟶ Adenosine diphosphate + Phosphorylcholine
- Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:1(9Z)):
Adenosine triphosphate + Choline ⟶ Adenosine diphosphate + Phosphorylcholine
- Phosphatidylcholine Biosynthesis PC(18:1(9Z)/18:1(9Z)):
Adenosine triphosphate + Choline ⟶ Adenosine diphosphate + Phosphorylcholine
PharmGKB(0)
1 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Angela C Brown, Kathleen Boesze-Battaglia, Nataliya V Balashova, Nestor Mas Gómez, Kaye Speicher, Hsin-Yao Tang, Margaret E Duszyk, Edward T Lally. Membrane localization of the Repeats-in-Toxin (RTX) Leukotoxin (LtxA) produced by Aggregatibacter actinomycetemcomitans.
PloS one.
2018; 13(10):e0205871. doi:
10.1371/journal.pone.0205871
. [PMID: 30335797] - M J Darkes, S M Davies, J P Bradshaw. X-ray diffraction study of feline leukemia virus fusion peptide and lipid polymorphism.
FEBS letters.
1999 Nov; 461(3):178-82. doi:
10.1016/s0014-5793(99)01454-4
. [PMID: 10567693] - Z Zhou, B G Sayer, D W Hughes, R E Stark, R M Epand. Studies of phospholipid hydration by high-resolution magic-angle spinning nuclear magnetic resonance.
Biophysical journal.
1999 Jan; 76(1 Pt 1):387-99. doi:
10.1016/s0006-3495(99)77205-x
. [PMID: 9876150] - S M Davies, R F Epand, J P Bradshaw, R M Epand. Modulation of lipid polymorphism by the feline leukemia virus fusion peptide: implications for the fusion mechanism.
Biochemistry.
1998 Apr; 37(16):5720-9. doi:
10.1021/bi980227v
. [PMID: 9548958] - Z J Chen, L C Van Gorkom, R M Epand, R E Stark. Nuclear magnetic resonance studies of lipid hydration in monomethyldioleoylphosphatidylethanolamine dispersions.
Biophysical journal.
1996 Mar; 70(3):1412-8. doi:
10.1016/s0006-3495(96)79700-x
. [PMID: 8785297] - A R Dentino, P W Westerman, P L Yeagle. A study of carbobenzoxy-D-phenylalanine-L-phenylalanine-glycine, an inhibitor of membrane fusion, in phospholipid bilayers with multinuclear magnetic resonance.
Biochimica et biophysica acta.
1995 May; 1235(2):213-20. doi:
10.1016/0005-2736(95)80007-3
. [PMID: 7756328] - R M Epand, R F Epand. Calorimetric detection of curvature strain in phospholipid bilayers.
Biophysical journal.
1994 May; 66(5):1450-6. doi:
10.1016/s0006-3495(94)80935-x
. [PMID: 8061194] - P L Yeagle, F T Smith, J E Young, T D Flanagan. Inhibition of membrane fusion by lysophosphatidylcholine.
Biochemistry.
1994 Feb; 33(7):1820-7. doi:
10.1021/bi00173a027
. [PMID: 8110784] - T Stegmann. Membrane fusion-inhibiting peptides do not inhibit influenza virus fusion or the Ca(2+)-induced fusion of negatively charged vesicles.
The Journal of biological chemistry.
1993 Dec; 268(36):26886-92. doi:
NULL
. [PMID: 8262922] - R M Epand, R F Epand, C D Richardson, P L Yeagle. Structural requirements for the inhibition of membrane fusion by carbobenzoxy-D-Phe-Phe-Gly.
Biochimica et biophysica acta.
1993 Oct; 1152(1):128-34. doi:
10.1016/0005-2736(93)90239-v
. [PMID: 8399290] - R F Epand, C B Xue, S H Wang, F Naider, J M Becker, R M Epand. Role of prenylation in the interaction of the a-factor mating pheromone with phospholipid bilayers.
Biochemistry.
1993 Aug; 32(32):8368-73. doi:
10.1021/bi00083a041
. [PMID: 8347633] - K Boesze-Battaglia, S J Fliesler, J Li, J E Young, P L Yeagle. Retinal and retinol promote membrane fusion.
Biochimica et biophysica acta.
1992 Nov; 1111(2):256-62. doi:
10.1016/0005-2736(92)90318-g
. [PMID: 1420260] - L C van Gorkom, S Q Nie, R M Epand. Hydrophobic lipid additives affect membrane stability and phase behavior of N-monomethyldioleoylphosphatidylethanolamine.
Biochemistry.
1992 Jan; 31(3):671-7. doi:
10.1021/bi00118a006
. [PMID: 1731922]