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J. Biol. Chem., Vol. 266, Issue 30, 19882-19885, 10, 1991

Mitochondrial phosphate transport. The Saccharomyces cerevisiae (threonine 43 to cysteine) mutant protein explicitly identifies transport with genomic sequence

A Phelps and H Wohlrab
Boston Biomedical Research Institute, Harvard Medical School, Massachusetts 02114.

The yeast mitochondrial phosphate transport protein (PTP) has only 38% sequence similarity to the bovine heart protein, and it has recently been postulated to code for a mitochondrial import receptor. Since the reconstitutively active protein is not completely pure, it is important to demonstrate explicitly that the yeast gene codes for PTP. We have replaced Thr43 with Cys (T43C) and show that its unidirectional and pH gradient-dependent inorganic phosphate transport activity becomes highly sensitive to N-ethylmaleimide. This new PTP/T43C catalyzes less than 10% of the wild type transport activity (1 mM [Pi]e, pHe (6.80); 0 mM [Pi]i, pHi (8.07); 30 s [Pi] uptake) suggesting that Thr43 occupies an important position in the PTP.
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A. Schroers, A. Burkovski, H. Wohlrab, and R. Kramer
The Phosphate Carrier from Yeast Mitochondria. DIMERIZATION IS A PREREQUISITE FOR FUNCTION
J. Biol. Chem., June 5, 1998; 273(23): 14269 - 14276.
[Abstract] [Full Text] [PDF]


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J. Biol. Chem.Home page
A. Schroers, R. Kramer, and H. Wohlrab
The Reversible Antiport-Uniport Conversion of the Phosphate Carrier from Yeast Mitochondria Depends on the Presence of a Single Cysteine
J. Biol. Chem., April 18, 1997; 272(16): 10558 - 10564.
[Abstract] [Full Text] [PDF]




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