| General Information of MET (ID: META00437) |
| Name |
Pyridoxal 5'-phosphate
|
| Synonyms |
Click to Show/Hide Synonyms of This Metabolite
3-Hydroxy-2-methyl-5-[(phosphonooxy)methyl]-4-pyridinecarboxaldehyde; 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde 5-phosphate; Biosechs; Codecarboxylase; Coenzyme b6; Hairoxal; Hexermin-p; Hi-pyridoxin; Hiadelon; Himitan; PAL-p; PLP', Pyridoxal 5'-(dihydrogen phosphate), 'Pyridoxal 5-monophosphoric acid ester; Phosphate mono-(4-formyl-5-hydroxy-6-methyl-pyridin-3-ylmethyl) ester', Pyridoxal 5'-(dihydrogen phosphoric acid), 'Pyridoxal 5-monophosphate ester; Phosphate, pyridoxal; Phosphopyridoxal; Phosphopyridoxal coenzyme; Phosphoric acid mono-(4-formyl-5-hydroxy-6-methyl-pyridin-3-ylmethyl) ester; Pidopidon; Piodel; Pydoxal; Pyridoxal 5 phosphate; Pyridoxal 5-phosphate; Pyridoxal 5-phosphoric acid; Pyridoxal p; Pyridoxal phosphate', PYRIDOXAL-5'-phosphATE, '3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde 5-phosphoric acid; Pyridoxal phosphoric acid', PYRIDOXAL-5'-phosphoric acid, Pyridoxal 5'-phosphoric acid, 'Apolon b6; Pyridoxal-p; Pyridoxyl phosphate; Pyromijin; Sechvitan; Vitahexin-p; Vitazechs
|
| Source |
Endogenous;Escherichia Coli Metabolite;Yeast Metabolite;Food;Drug;Cosmetic;Microbial
|
| Structure Type |
Pyridine carboxaldehydes (Click to Show/Hide the Complete Structure Type Hierarchy)
Organoheterocyclic compounds
Pyridines and derivatives
Pyridine carboxaldehydes
|
| PubChem CID |
|
| HMDB ID |
|
| Formula |
C8H10NO6P
|
| Structure |
<iframe style="width: 300px; height: 300px;" frameborder="0" src="https://embed.molview.org/v1/?mode=balls&cid=1051"></iframe>
|
 |
|
3D MOL
|
2D MOL
|
|
Click to Show/Hide the Molecular/Functional Data (External Links/Property/Function) of This Metabolite
|
| KEGG ID |
|
| DrugBank ID |
|
| ChEBI ID |
|
| FooDB ID |
|
| ChemSpider ID |
|
| METLIN ID |
|
| Physicochemical Properties |
Molecular Weight |
247.14 |
Topological Polar Surface Area |
117 |
| XlogP |
-1.1 |
Complexity |
292 |
| Heavy Atom Count |
16 |
Rotatable Bond Count |
4 |
| Hydrogen Bond Donor Count |
3 |
Hydrogen Bond Acceptor Count |
7 |
| Function |
This is the active form of vitamin B6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (pyridoxamine). -- Pubchem; Pyridoxal-phosphate (PLP, pyridoxal-5'-phosphate) is a cofactor of many enzymatic reactions. It is the active form of vitamin B6 which comprises three natural organic compounds, pyridoxal, pyridoxamine and pyridoxine. -- Wikipedia.
|
|
Regulatory Network
|
|
|
|
|
|
|
|
|
click to show the details of this protein
Induced Change
