Phosphoserine (abbreviated as SEP or J) is an ester of serine and phosphoric acid. Phosphoserine is a component of many proteins as the result of posttranslational modifications. The phosphorylation of the alcohol functional group in serine to produce phosphoserine is catalyzed by various types of kinases. Through the use of technologies that utilize an expanded genetic code, phosphoserine can also be incorporated into proteins during translation.
It is a normal metabolite found in human biofluids.
Phosphoserine has three potential coordination sites (carboxyl, amine and phosphate group) Determination of the mode of coordination between phosphorylated ligands and metal ions occurring in an organism is a first step to explain the function of the phosphoserine in bioinorganic processes. |
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InChI=1S/C8H20NO6P/c1-9(2,3)4-5-14-16(12,13)15-7-8(11)6-10/h8,10-11H,4-7H2,1-3H3/t8-/m1/s1 |
SUHOQUVVVLNYQR-MRVPVSSYSA-N |
C[N+](C)(C)CCOP([O-])(=O)OC[C@H](O)CO |
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Mus musculus
(NCBI:txid10090)
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Source: BioModels - MODEL1507180067
See:
PubMed
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Saccharomyces cerevisiae
(NCBI:txid4932)
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Source: yeast.sf.net
See:
PubMed
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Escherichia coli
(NCBI:txid562)
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See:
PubMed
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Homo sapiens
(NCBI:txid9606)
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See:
DOI
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Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
parasympatholytic
Any cholinergic antagonist that inhibits the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the muscarinic antagonists.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
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parasympatholytic
Any cholinergic antagonist that inhibits the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the muscarinic antagonists.
neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
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View more via ChEBI Ontology
(2R)-2,3-dihydroxypropyl 2-(trimethylazaniumyl)ethyl phosphate
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2- {[(2R)- 2,3- dihydroxypropoxy](hydroxy)phosphoryloxy}- N,N,N- trimethylethanaminium
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alfoscerate de choline
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ChemIDplus
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alfoscerato de colina
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ChemIDplus
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choline alfoscerate
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ChemIDplus
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choline alfoscerate
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KEGG DRUG
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cholini alfosceras
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ChemIDplus
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(2R)-2,3-dihydroxypropyl 2-(trimethylammonio)ethyl phosphate
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IUPAC
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alpha-Glycerophosphorylcholine
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HMDB
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Choline alphoscerate
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ChemIDplus
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Choline glycerophosphate
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ChemIDplus
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Cholini glycerophosphas
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ChemIDplus
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Glicerofosfato de colina
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ChemIDplus
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Glycerol phosphorylcholine
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HMDB
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Glycerol-3-phosphatidylcholine
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HMDB
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glycerol-3-phosphocholine
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ChEBI
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Glycerophosphate de choline
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ChemIDplus
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Glycerophosphocholine
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ChemIDplus
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Glycerophosphocholine
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KEGG COMPOUND
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Glycerophosphocholine
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KEGG COMPOUND
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Glycerophosphorylcholine
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ChemIDplus
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GPCho
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HMDB
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L-alpha-Glycerophosphocholine
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ChemIDplus
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L-alpha-Glycerophosphorylcholine
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ChemIDplus
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L-alpha-Glycerophosphorylcholine
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HMDB
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L-Choline hydroxide 2,3-dihydroxypropyl hydrogen phosphate inner salt
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HMDB
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sn-3-GPC
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MetaCyc
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sn-Glycero-3-phosphocholine
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ChemIDplus
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sn-glycero-3-phosphocholine
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ChEBI
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sn-glycero-3-phosphocholine
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ChEBI
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sn-glycerol 3-phosphocholine
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UniProt
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28319-77-9
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CAS Registry Number
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ChemIDplus
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28319-77-9
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CAS Registry Number
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KEGG DRUG
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3908444
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Reaxys Registry Number
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Reaxys
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6062450
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Beilstein Registry Number
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Beilstein
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21165396
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PubMed citation
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Europe PMC
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21195433
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PubMed citation
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Europe PMC
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22191561
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PubMed citation
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Europe PMC
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22677751
|
PubMed citation
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Europe PMC
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22679745
|
PubMed citation
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Europe PMC
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22959283
|
PubMed citation
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Europe PMC
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23013274
|
PubMed citation
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SUBMITTER
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23244432
|
PubMed citation
|
Europe PMC
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23268258
|
PubMed citation
|
Europe PMC
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23314552
|
PubMed citation
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Europe PMC
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23387341
|
PubMed citation
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Europe PMC
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23528493
|
PubMed citation
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Europe PMC
|
24156263
|
PubMed citation
|
Europe PMC
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24166560
|
PubMed citation
|
Europe PMC
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6420466
|
PubMed citation
|
Europe PMC
|
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