Erythrosin 5′‐isothiocyanate labels Cys<sup>549</sup> as part of the low‐affinity ATP binding site of Na<sup>+</sup>/K<sup>+</sup>‐ATPase<sup>1</sup>

Holger Linnertz, Holger Kost, Tomáš Obšil, Arnošt Kotyk, Evžen Amler, Wilhelm Schoner

FEBS Letters · 1998 · 14 citations · 20 references

Abstract

The high-affinity E1ATP site of Na+/K+-ATPase labeled with fluorescein 5'-isothiocyanate and its E2ATP site labeled with erythrosin 5'-isothiocyanate (ErITC), as was shown recently [Linnertz et al. (1998) J. Biol. Chem. 273, 28813-28821], reside on separate and adjacent catalytic alpha subunits. This paper provides evidence that specific labeling of the E2ATP binding site with ErITC resulted in a modification of the Cys549 residue in the tryptic fragment with the sequence Val545-Leu-Gly-Phe-Cys549-His550. Hence, Cys549 is part of or close to the low-affinity E2ATP binding site of Na+/K+-ATPase.

References

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