Critical Domains within the Sequence of Human Organic Anion Transporting Polypeptides

ISSN: 1875-5453 (Online)
ISSN: 1389-2002 (Print)

Volume 16, 10 Issues, 2015

Download PDF Flyer

Current Drug Metabolism

Aims & ScopeAbstracted/Indexed in

Ranking and Category:
  • 101th of 291 in Biochemistry & Molecular Biology
  • 54th of 254 in Pharmacology & Pharmacy

Submit Abstracts Online Submit Manuscripts Online

Chandra Prakash
Department of Drug Metabolism and Pharmacokinetics Biogen Idec Cambridge

View Full Editorial Board

Subscribe Purchase Articles Order Reprints

Current: 3.487
5 - Year: 4.205

Critical Domains within the Sequence of Human Organic Anion Transporting Polypeptides

Author(s): Mei Hong

Affiliation: College of Life Science, South China Agricultural University, Guangzhou, China.


Organic anion-transporting polypeptides (human OATPs; other species Oatps; gene family SLC21/SLCO) play important roles in drug absorption and distribution. In recent years, much information has been obtained on substrates that are transported by OATPs. Computer-based hydropathy analysis predicts that OATP family members share several structural features including twelve transmembrane domains (TMs), conserved cysteine residues at extracellular loop 5, glycosylation sites, PDZ binding domains as well as putative phosphorylation sites. Studies on transmembrane domains have identified several amino acids that are essential for substrate uptake; while mutation of the conserved cysteine residues and glycosylation sites resulted in mis-processing transporter proteins. The interaction with PDZ proteins and phosphorylation modification of OATPs, on the other hand, mainly regulate the trafficking of these transporters. Although progress has been made on revealing the critical domains of OATPs, information is still limited and more studies on these aspects are needed. A better understanding of the important structural domains of OATPs will shed light on future targeted drug design and a more in-depth analysis of inter-individual variability of drug disposition.

Keywords: Conserved regions, glycosylation sites, organic anion transporting polypeptides, PDZ domains, phosphorylation, transmembrane domains.

Download Free Order Reprints Order Eprints Rights and Permissions


Article Details

Volume: 15
Issue Number: 3
First Page: 265
Last Page: 270
Page Count: 6
DOI: 10.2174/1389200214666131229111118

Related Journals

Webmaster Contact: Copyright © 2015 Bentham Science