Literature DB >> 11571301

A three-dimensional model of the human facilitative glucose transporter Glut1.

F A Zuniga1, G Shi, J F Haller, A Rubashkin, D R Flynn, P Iserovich, J Fischbarg.   

Abstract

The human facilitative transporter Glut1 is the major glucose transporter present in all human cells, has a central role in metabolism, and is an archetype of the superfamily of major protein facilitators. Here we describe a three-dimensional structure of Glut1 based on helical packing schemes proposed for lactose permease and Glut1 and predictions of secondary structure, and refined using energy minimization, molecular dynamics simulations, and quality and environmental scores. The Ramachandran scores and the stereochemical quality of the structure obtained were as good as those for the known structures of the KcsA K(+) channel and aquaporin 1. We found two channels in Glut1. One of them traverses the structure completely, and is lined by many residues known to be solvent-accessible. Since it is delimited by the QLS motif and by several well conserved residues, it may serve as the substrate transport pathway. To validate our structure, we determined the distance between these channels and all the residues for which mutations are known. From the locations of sugar transporter signatures, motifs, and residues important to the transport function, we find that this Glut1 structure is consistent with mutagenesis and biochemical studies. It also accounts for functional deficits in seven pathogenic mutants.

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Year:  2001        PMID: 11571301     DOI: 10.1074/jbc.M107350200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  15 in total

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4.  Structural signatures and membrane helix 4 in GLUT1: inferences from human blood-brain glucose transport mutants.

Authors:  Juan M Pascual; Dong Wang; Ru Yang; Lei Shi; Hong Yang; Darryl C De Vivo
Journal:  J Biol Chem       Date:  2008-04-03       Impact factor: 5.157

5.  Predicting the three-dimensional structure of the human facilitative glucose transporter glut1 by a novel evolutionary homology strategy: insights on the molecular mechanism of substrate migration, and binding sites for glucose and inhibitory molecules.

Authors:  Alexis Salas-Burgos; Pavel Iserovich; Felipe Zuniga; Juan Carlos Vera; Jorge Fischbarg
Journal:  Biophys J       Date:  2004-08-23       Impact factor: 4.033

6.  Molecular dynamics simulation studies of GLUT4: substrate-free and substrate-induced dynamics and ATP-mediated glucose transport inhibition.

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7.  Piracetam and TRH analogues antagonise inhibition by barbiturates, diazepam, melatonin and galanin of human erythrocyte D-glucose transport.

Authors:  Richard J Naftalin; Philip Cunningham; Iram Afzal-Ahmed
Journal:  Br J Pharmacol       Date:  2004-05-17       Impact factor: 8.739

8.  Interactions of ATP, oestradiol, genistein and the anti-oestrogens, faslodex (ICI 182780) and tamoxifen, with the human erythrocyte glucose transporter, GLUT1.

Authors:  Iram Afzal; Philip Cunningham; Richard J Naftalin
Journal:  Biochem J       Date:  2002-08-01       Impact factor: 3.857

Review 9.  Vitamin C transporters.

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Journal:  J Physiol Biochem       Date:  2008-12       Impact factor: 4.158

10.  An insulin-like modular basis for the evolution of glucose transporters (GLUT) with implications for diabetes.

Authors:  Robert Root-Bernstein
Journal:  Evol Bioinform Online       Date:  2007-10-15       Impact factor: 1.625

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