Biology:SLC22A1

From HandWiki
Short description: Protein-coding gene in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Solute carrier family 22 member 1 is a protein that in humans is encoded by the gene SLC22A1.[1][2]

Function

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. Two transcript variants encoding two different isoforms have been found for this gene, but only the longer variant encodes a functional transporter.[2]

It is also required for the uptake of metformin by cells.[3][4]

See also

References

  1. "The two human organic cation transporter genes SLC22A1 and SLC22A2 are located on chromosome 6q26". Cytogenetics and Cell Genetics 79 (3–4): 198–200. Jun 1998. doi:10.1159/000134720. PMID 9605850. 
  2. 2.0 2.1 "Entrez Gene: SLC22A1 solute carrier family 22 (organic cation transporter), member 1". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6580. 
  3. Pryor, R; Cabreiro, F; Haberland, G (16 October 2015). "Repurposing metformin: an old drug with new tricks in its binding pockets". Biochemical Journal 471 (3): 307–322. doi:10.1042/BJ20150497. PMID 26475449. 
  4. Rosilio, C; Ben-Sahra, I; Bost, F; Peyron, JF (1 May 2014). "Metformin: a metabolic disruptor and anti-diabetic drug to target human leukemia.". Cancer Letters 346 (2): 188–96. doi:10.1016/j.canlet.2014.01.006. PMID 24462823. 

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.