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Cloning and functional expression of ATA1, a subtype of amino acid transporter A, from human placenta

  • Haiping Wang
    ,
  • Wei Huang
    ,
  • Mitsuru Sugawara
    ,
  • Lawrence D Devoe
    ,
  • Frederick H. Leibach
    ,
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

This report describes the primary structure and functional characteristics of human ATA1, a subtype of the amino acid transport system A. The human ATA1 cDNA was isolated from a placental cDNA library. The cDNA codes for a protein of 487 amino acids with 11 putative transmembrane domains. The transporter mRNA (~ 9.0 kb) is expressed most prominently in the placenta and heart, but detectable level of expression is evident in other tissues including the brain. When expressed heterologously in mammalian cells, the cloned transporter mediates Na+-coupled transport of the system A-specific model substrate α-(methylamino)isobutyric acid. The transport process is saturable with a Michaelis-Menten constant of 0.89 ± 0.12 mM. The Na+:amino acid stoichiometry is 1:1 as deduced from the Na+-activation kinetics. The transporter is specific for small short-chain neutral amino acids. The gene for the transporter is located on human chromosome 12. (C) 2000 Academic Press.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1175-1179 (5 pages)

Journal (Volume, Issue Number)

Biochemical and Biophysical Research Communications (Volume 273, Issue 3)

Publication milestones

  • Published - 07/14/2000

Publication status

Published - 07/14/2000

ISSN

0006-291X

Publication IDs

  • Scopus: 0034647586
  • PubMed: 10891391

Publication metrics

Metrics

SciVal
citations
89
SciVal
FWCI
2.91
SciVal
Author count
7
SciVal
Paper percentile
92
SciVal
Top percentile
10
Scopus
citations
Fractional count
2
Fractional count
0.29
Fractional count
5
Fractional count
0.71
Fractional count
2
Fractional count
1

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Mentions
2
Citation count
104
Captures
31

Funding Details

This work was supported by National Institutes of Health Grants DA 10045 and HD 33347. The authors thank Vickie Mitchell for excellent secretarial assistance.
FundersFunding numbers
NIH
HD 33347
NIDA
R01DA010045