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PMID: 8550601 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Cloning and membrane topology of a P type ATPase from Helicobacter pylori.

The Journal of biological chemistry ·Vol. 271 ·No. 1 ·1996-01-05 ·Pages 446-57

Melchers K, Weitzenegger T, Buhmann A, Steinhilber W, Sachs G, Schäfer KP

Abstract

Southern blot screening of a genomic Helicobacter pylori library was employed to find a P type ATPase using a mixture of 16 DNA oligonucleotides coding for the DKTGT(I/L)T consensus sequence specific for the phosphorylation site of this family of ATPases. A positive clone, pRH439, was isolated and sequenced. The inserted 3.4-kb H. pylori DNA contained an intact open reading frame encoding a protein of 686 amino acids carrying the consensus sites for phosphorylation and ATP binding. The amino acid sequence exhibits a 25-30% identity with bacterial Cd2+ and Cu2+ ATPases. Genomic Southern blot analysis showed that this ATPase was present in all H. pylori strains examined, whereas it was not detectable in Campylobacter jejuni and other bacteria. The membrane topology of this ATPase was investigated using in vitro transcription/translation of fusion vectors to find signal anchor and/or stop transfer sequences. Eight regions of the H. pylori ATPase acted as signal anchor and/or stop transfer sequences and were ordered pairwise along the polypeptide chain placing the N and C-terminal amino acids in the cytoplasm. These transmembrane segments are contained between positions 73 and 92 (H1), 98 and 125 (H2), 128 and 148 (H3), 149 and 176 (H4), 309 and 327 (H5), 337 and 371 (H6), 637 and 658 (H7), and 659 and 685 (H8). The membrane domain of the ATPase, therefore, consists of at least four pairs of transmembrane segments with the phosphorylation site and ATP binding domain located in the large cytoplasmic loop between H6 and H7. The cytoplasmic domain contains several histidines and cysteines, perhaps indicative of divalent cation binding sites. There are several charged amino acids (3 Lys, 2 Glu, 2 Asp), predicted to be in the membrane domain mainly in H2, H3, and H4 and a Cys-Pro-Cys putative metal ion site in H6. The extracytoplasmic domain also has several charged amino acids (5 Glu, 1 Asp, 1 Lys, 1 Arg). It is likely that this novel protein is a heavy metal cation transporting ATPase and belongs to a family of P type ATPases containing eight transmembrane segments.

MeSH Terms
Adenosine Triphosphatases/genetics,metabolism Amino Acid Sequence Base Sequence Binding Sites Cations, Divalent Cell Membrane/enzymology Cloning, Molecular DNA, Bacterial Genetic Vectors Helicobacter pylori/enzymology,metabolism Molecular Sequence Data Protein Biosynthesis Sequence Homology, Amino Acid Transcription, Genetic
Chemicals
Cations, Divalent DNA, Bacterial Adenosine Triphosphatases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Melchers K
Byk Gulden Pharmaceuticals, Department of Molecular Biology, Konstanz, Germany.
Weitzenegger T
Buhmann A
Steinhilber W
Sachs G
Schäfer K P
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1996-01-05
Pages
446-57
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · DK40615 · United States
NIDDK NIH HHS · DK41301 · United States
NIDDK NIH HHS · DK46917 · United States
Databases
GENBANK
L46864, U59625
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