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      The Major Facilitator Superfamily (MFS) Revisited

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          Abstract

          The Major Facilitator Superfamily (MFS) is the largest known superfamily of secondary carriers found in the biosphere. It is ubiquitously distributed throughout virtually all currently recognized organismal phyla. This superfamily currently (2012) consists of 74 families, each of which is usually concerned with transport of a certain type of substrate. Many of these families, defined phylogenetically, do not include even a single member that is functionally characterized. In this article we probe the evolutionary origins of these transporters, providing evidence that they arose from a single 2 TMS hairpin structure that triplicated to give a 6 TMS unit that duplicated to a 12 TMS protein, the most frequent topological type of these permeases. We globally examine MFS protein topologies, focusing on exceptional proteins that deviate from the norm. Nine distantly related families appear to have members with 14 TMSs where the extra two are usually centrally localized between the two 6 TMS repeat units. They probably have arisen by intragenic duplication of an adjacent hairpin. This alternative topology probably arose multiple times during MFS evolution. Convincing evidence for MFS permeases with fewer than 12 TMSs was not forthcoming, leading to the suggestion that all 12 TMSs are required for optimal function. Some homologues appear to have 13, 14, 15 or 16 TMSs, and the probable locations of the extra TMSs were identified. A few MFS permeases are fused to other functional domains or are fully duplicated to give 24 TMS proteins with dual functions. Finally, the MFS families with no known function were subjected to genomic context analyses leading to functional predictions.

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          Author and article information

          Journal
          101229646
          32231
          FEBS J
          FEBS J.
          The FEBS journal
          1742-464X
          1742-4658
          1 August 2012
          08 May 2012
          June 2012
          01 June 2013
          : 279
          : 11
          : 2022-2035
          Affiliations
          Division of Biological Sciences, University of California at San Diego, La Jolla, CA 92093-0116
          Author notes
          [* ]Corresponding author: Telephone: (858) 534-4084, Fax: (858) 534-7108, msaier@ 123456ucsd.edu
          [§]

          These two authors contributed equally to the work reported herein.

          Article
          PMC3425384 PMC3425384 3425384 nihpa368601
          10.1111/j.1742-4658.2012.08588.x
          3425384
          22458847
          77512413-0e09-47b5-a214-6a0772ecb1a6
          History
          Funding
          Funded by: National Institute of General Medical Sciences : NIGMS
          Award ID: R01 GM077402 || GM
          Categories
          Article

          evolution,Transport proteins,secondary active transport,MFS,multi-drug resistance,uptake/efflux,superfamily

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