Literature DB >> 19031293

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

Juke S Lolkema1, Dirk-Jan Slotboom.   

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.

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Year:  2008        PMID: 19031293     DOI: 10.1080/09687680802541177

Source DB:  PubMed          Journal:  Mol Membr Biol        ISSN: 0968-7688            Impact factor:   2.857


  18 in total

1.  Substrate binding tunes conformational flexibility and kinetic stability of an amino acid antiporter.

Authors:  Christian A Bippes; Antra Zeltina; Fabio Casagrande; Merce Ratera; Manuel Palacin; Daniel J Muller; Dimitrios Fotiadis
Journal:  J Biol Chem       Date:  2009-05-06       Impact factor: 5.157

2.  AlignMe--a membrane protein sequence alignment web server.

Authors:  Marcus Stamm; René Staritzbichler; Kamil Khafizov; Lucy R Forrest
Journal:  Nucleic Acids Res       Date:  2014-04-21       Impact factor: 16.971

Review 3.  The rocking bundle: a mechanism for ion-coupled solute flux by symmetrical transporters.

Authors:  Lucy R Forrest; Gary Rudnick
Journal:  Physiology (Bethesda)       Date:  2009-12

4.  Membrane topological structure of neutral system N/A amino acid transporter 4 (SNAT4) protein.

Authors:  Qian Shi; Rugmani Padmanabhan; Carla J Villegas; Sumin Gu; Jean X Jiang
Journal:  J Biol Chem       Date:  2011-09-14       Impact factor: 5.157

5.  Cloning, expression, and functional characterization of secondary amino acid transporters of Lactococcus lactis.

Authors:  Hein Trip; Niels L Mulder; Juke S Lolkema
Journal:  J Bacteriol       Date:  2012-11-09       Impact factor: 3.490

Review 6.  Structural perspectives on secondary active transporters.

Authors:  Olga Boudker; Grégory Verdon
Journal:  Trends Pharmacol Sci       Date:  2010-07-23       Impact factor: 14.819

7.  Structure and mechanism of a Na+-independent amino acid transporter.

Authors:  Paul L Shaffer; April Goehring; Aruna Shankaranarayanan; Eric Gouaux
Journal:  Science       Date:  2009-07-16       Impact factor: 47.728

Review 8.  Structure and function of Na(+)-symporters with inverted repeats.

Authors:  Jeff Abramson; Ernest M Wright
Journal:  Curr Opin Struct Biol       Date:  2009-07-22       Impact factor: 6.809

9.  Molecular basis of transport and regulation in the Na(+)/betaine symporter BetP.

Authors:  Susanne Ressl; Anke C Terwisscha van Scheltinga; Clemens Vonrhein; Vera Ott; Christine Ziegler
Journal:  Nature       Date:  2009-03-05       Impact factor: 49.962

10.  Structure of a prokaryotic virtual proton pump at 3.2 A resolution.

Authors:  Yiling Fang; Hariharan Jayaram; Tania Shane; Ludmila Kolmakova-Partensky; Fang Wu; Carole Williams; Yong Xiong; Christopher Miller
Journal:  Nature       Date:  2009-07-05       Impact factor: 49.962

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