| Literature DB >> 31519459 |
Rachel-Ann A Garibsingh1, Avner Schlessinger2.
Abstract
There are over 420 human solute carrier (SLC) transporters from 65 families that are expressed ubiquitously in the body. The SLCs mediate the movement of ions, drugs, and metabolites across membranes and their dysfunction has been associated with a variety of diseases, such as diabetes, cancer, and central nervous system (CNS) disorders. Thus, SLCs are emerging as important targets for therapeutic intervention. Recent technological advances in experimental and computational biology allow better characterization of SLC pharmacology. Here we describe recent approaches to modulate SLC transporter function, with an emphasis on the use of computational approaches and computer-aided drug design (CADD) to study nutrient transporters. Finally, we discuss future perspectives in the rational design of SLC drugs.Entities:
Keywords: computer-aided drug design; membrane transporter; protein structure prediction; solute carrier; structure-based drug discovery
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Year: 2019 PMID: 31519459 PMCID: PMC7082830 DOI: 10.1016/j.tips.2019.08.006
Source DB: PubMed Journal: Trends Pharmacol Sci ISSN: 0165-6147 Impact factor: 14.819