Nucleotide-binding sites in V-type Na+-ATPase from Enterococcus hirae

J Biochem. 2002 Nov;132(5):789-94. doi: 10.1093/oxfordjournals.jbchem.a003288.

Abstract

Enterococcus hirae V-ATPase, in contrast to most V-type ATPases, is resistant to N-ethylmaleimide (NEM). Alignment of the amino acid sequences of NtpA suggests that the NEM-sensitive Cys of V-type ATPases is replaced by Ala in E. hirae V-ATPase. Consistent with this prediction, the V-ATPase became sensitive upon substitution of the Ala with Cys. The three-dimensional structure of the NtpB subunit of V-ATPase was modeled based on the structure of the corresponding subunit (alpha subunit) of bovine F(1)-ATPase by homology modeling. Overall, the 3D structure of the subunit resembled that of alpha subunit of bovine F(1)-ATPase. The NtpB subunit, which lacks the P-loop consensus sequence for nucleotide binding, was predicted to bind a nucleotide at the modeled nucleotide-binding site. Experimental data supported the prediction that the E. hirae V-ATPase had about six nucleotide-binding sites.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Cattle
  • Enterococcus / metabolism*
  • Ethylmaleimide / pharmacology
  • Molecular Sequence Data
  • Proton-Translocating ATPases / metabolism
  • Sodium / metabolism
  • Sulfhydryl Reagents / pharmacology
  • Vacuolar Proton-Translocating ATPases / metabolism*

Substances

  • Sulfhydryl Reagents
  • Sodium
  • Adenosine Triphosphatases
  • Vacuolar Proton-Translocating ATPases
  • Proton-Translocating ATPases
  • Ethylmaleimide