The major amino acid transporter superfamily has a similar core structure as Na plus -galactose and Na plus -leucine transporters

Juke S. Lolkema*, Dirk-Jan Slotboom

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

35 Citations (Scopus)
329 Downloads (Pure)

Abstract

The sodium solute symporters (SSS) and neurotransmitter sodium symporters (NSS) are two families of secondary transporters that are not related in amino acid sequence. Nonetheless, recent crystal structures showed that the Na+/galactose (SSS) and Na+/leucine (NSS) transporters have similar core structures. The structural relatedness highlights the need for classification methods for membrane protein structures based on other criteria than amino acid similarity. Here, we demonstrate that a method based on hydropathy profile alignments convincingly identifies structural similarity between the NSS and SSS families. Most importantly, the method shows that one of the largest transporter families for which a crystal structure is elusive (the amino acid/polyamine/organocation or APC superfamily), also shares the similar core structure observed for the Na+/galactose and Na+/leucine transporters. The APC superfamily contains the major amino acid transporter families that are found throughout life. Insight into their structure will significantly facilitate the studies of this important group of transporters.

Original languageEnglish
Article number905963464
Pages (from-to)567-570
Number of pages4
JournalMolecular Membrane Biology
Volume25
Issue number6-7
DOIs
Publication statusPublished - 2008

Keywords

  • Transporter classification
  • transport protein structure
  • MemGen
  • hydropathy profile alignment
  • structural class
  • HYDROPATHY PROFILE ALIGNMENT
  • MEMBRANE-PROTEINS
  • CRYSTAL-STRUCTURE
  • ESCHERICHIA-COLI
  • MECHANISM
  • HOMOLOG
  • FAMILY

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