HOAT1: Difference between revisions

From Proteopedia
Jump to navigationJump to search
New page: Interactive 3D Complement in Proteopedia<br> <table width="95%" border="0"><tr><td> {| align="left" |- | <imagemap> Image:Cell press logo.png|2...
 
No edit summary
Line 38: Line 38:
Pelis, R.M. (2014). A plasma concentration of α-ketoglutarate influences
Pelis, R.M. (2014). A plasma concentration of α-ketoglutarate influences
the kinetic interaction of ligands with organic anion transporter 1. Mol.
the kinetic interaction of ligands with organic anion transporter 1. Mol.
Pharmacol. 86, 86–95. https://doi.org/10.1124/mol.114.091777.</ref>OAT1 also plays a key role in excreting waste from organic drug metabolism and
Pharmacol. 86, 86–95. https://doi.org/10.1124/mol.114.091777.</ref> <ref>Uwai, Y., Kawasaki, T., and Nabekura, T. (2017). D-Malate decreases renal
content of α-ketoglutarate, a driving force of organic anion transporters
OAT1 and OAT3, resulting in inhibited tubular secretion of phenolsulfonphthalein,
in rats. Biopharm. Drug Dispos. 38, 479–485. https://doi.org/10.
1002/bdd.2089.</ref>OAT1 also plays a key role in excreting waste from organic drug metabolism and
contributes significantly to drug-drug interactions and drug disposition. However, the structural basis of specific
contributes significantly to drug-drug interactions and drug disposition. However, the structural basis of specific
substrate and inhibitor transport by human OAT1 (hOAT1) has remained elusive. Here are four
substrate and inhibitor transport by human OAT1 (hOAT1) has remained elusive. Here are four