Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1994-3-4
pubmed:abstractText
In the insulin-responsive tissues, muscle and adipose, the GLUT4 glucose transporter isoform accounts for most of the increase in hexose flux in response to hormone. In these cell types, as well as in fibroblasts transfected with cDNAs encoding the transporters, GLUT1 and GLUT4 are sorted to different subcellular locations. In the latter, GLUT1 is found primarily at the cell surface whereas GLUT4 localizes to the interior of the cell in a perinuclear distribution. The construction and analysis of chimeras of these two transporter isoforms have allowed identification of the COOH-terminal 30 amino acids as a critical sorting signal for differential localization of the transporters. In this study, we show that 2 residues present in the GLUT4 COOH terminus, Leu-489 and Leu-490, are critical for the intracellular sequestration of this isoform in NIH3T3 cells.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Glucose Transporter Type 1, http://linkedlifedata.com/resource/pubmed/chemical/Glucose Transporter Type 4, http://linkedlifedata.com/resource/pubmed/chemical/Leucine, http://linkedlifedata.com/resource/pubmed/chemical/Monosaccharide Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Muscle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Protein Sorting Signals, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SLC2A1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/SLC2A4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Slc2a1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Slc2a1 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Slc2a4 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Slc2a4 protein, rat
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
28
pubmed:volume
269
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2353-6
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:8300557-3T3 Cells, pubmed-meshheading:8300557-Amino Acid Sequence, pubmed-meshheading:8300557-Animals, pubmed-meshheading:8300557-Glucose Transporter Type 1, pubmed-meshheading:8300557-Glucose Transporter Type 4, pubmed-meshheading:8300557-Humans, pubmed-meshheading:8300557-Leucine, pubmed-meshheading:8300557-Mice, pubmed-meshheading:8300557-Molecular Sequence Data, pubmed-meshheading:8300557-Monosaccharide Transport Proteins, pubmed-meshheading:8300557-Muscle Proteins, pubmed-meshheading:8300557-Mutagenesis, Site-Directed, pubmed-meshheading:8300557-Point Mutation, pubmed-meshheading:8300557-Protein Conformation, pubmed-meshheading:8300557-Protein Sorting Signals, pubmed-meshheading:8300557-Rats, pubmed-meshheading:8300557-Recombinant Fusion Proteins, pubmed-meshheading:8300557-Sequence Homology, Amino Acid, pubmed-meshheading:8300557-Transfection
pubmed:year
1994
pubmed:articleTitle
A Leu-Leu sequence is essential for COOH-terminal targeting signal of GLUT4 glucose transporter in fibroblasts.
pubmed:affiliation
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't