General Information of MET (ID: META00275)
Name Potassium
Synonyms   Click to Show/Hide Synonyms of This Metabolite
K(+); K+; Kalium; LRF-1; LRF1 Transcription factor; Liver regeneration factor 1; Nabumeton a; POTASSIUM ion; Potassium (ion); Potassium (k+); Potassium cation; Potassium ion (K1+); Potassium ion (k+); Potassium ion(+); Potassium ion(1+); Potassium monocation; Potassium(+); Potassium(1+); Potassium(1+) ion; Potassium(I) cation
Source Exogenous;Escherichia Coli Metabolite;Food;Toxins/Pollutant;Microbial
Structure Type   Homogeneous alkali metal compounds  (Click to Show/Hide the Complete Structure Type Hierarchy)
Homogeneous metal compounds
Homogeneous alkali metal compounds
PubChem CID
813
HMDB ID
HMDB0000586
Formula
K
Structure
<iframe style="width: 300px; height: 300px;" frameborder="0" src="https://embed.molview.org/v1/?mode=balls&cid=813"></iframe>
3D MOL is unavailable 2D MOL
  Click to Show/Hide the Molecular/Functional Data (External Links/Property/Function) of This Metabolite
KEGG ID
C00238
ChEBI ID
29103
FooDB ID
FDB003521
METLIN ID
3197
Physicochemical Properties Molecular Weight 39.098 Topological Polar Surface Area N.A.
XlogP N.A. Complexity N.A.
Heavy Atom Count 1 Rotatable Bond Count N.A.
Hydrogen Bond Donor Count N.A. Hydrogen Bond Acceptor Count N.A.
Function
Potassium is an essential electrolyte. Potassium balance is crucial for regulating the excitability of nerves and muscles and so critical for regulating contractility of cardiac muscle. Although the most important changes seen in the presence of deranged potassium are cardiac, smooth muscle is also affected with increasing muscle weakness, a feature of both hyperkalaemia and hypokalaemia. Physiologically, it exists as an ion in the body. Potassium (K+) is a positively charged electrolyte, cation, which is present throughout the body in both intracellular and extracellular fluids. The majority of body potassium, >90%, are intracellular. It moves freely from intracellular fluid (ICF) to extracellular fluid (ECF) and vice versa when adenosine triphosphate increases the permeability of the cell membrane. It is mainly replaced inside or outside the cells by another cation, sodium (Na+). The movement of potassium into or out of the cells is linked to certain body hormones and also to certain physiological states. Standard laboratory tests measure ECF potassium. Potassium enters the body rapidly during food ingestion. Insulin is produced when a meal is eaten; this causes the temporary movement of potassium from ECF to ICF. Over the ensuing hours, the kidneys excrete the ingested potassium and homeostasis is returned. In the critically ill patient, suffering from hyperkalaemia, this mechanism can be manipulated beneficially by administering high concentration (50%) intravenous glucose. Insulin can be added to the glucose, but glucose alone will stimulate insulin production and cause movement of potassium from ECF to ICF. The stimulation of alpha receptors causes increased movement of potassium from ICF to ECF. A noradrenaline infusion can elevate serum potassium levels. An adrenaline infusion, or elevated adrenaline levels, can lower serum potassium levels. Metabolic acidosis causes a rise in extracellular potassium levels. In this situation, excess of hydrogen ions (H+) are exchanged for intracellular potassium ions, probably as a result of the cellular response to a falling blood pH. Metabolic alkalosis causes the opposite effect, with potassium moving into the cells.
Regulatory Network
Full List of Protein(s) Regulating This Metabolite
      Isomerases (EC 5)
            Alpha-methylacyl-CoA racemase (AMACR) Click to Show/Hide the Full List of Regulating Pair(s):   1 Pair(s)
               Detailed Information Protein   Info click to show the details of this protein
               Regulating Pair Experim Info click to show the details of experiment for validating this pair [1]
                      Introduced Variation Knockout of Amacr
                      Induced Change Potassium concentration: increase
                      Summary Introduced Variation         Induced Change 
                      Disease Status Healthy individual
                      Details It is reported that knockout of Amacr leads to the increase of potassium levels compared with control group.
References
1 Phytol is lethal for Amacr-deficient mice. Biochim Biophys Acta. 2015 Oct;1851(10):1394-405.

If you find any error in data or bug in web service, please kindly report it to Dr. Zhang and Dr. Mou.