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- W2110132014 abstract "Helicobacter pylori, strain 26695, has a circular genome of 1,667,867 base pairs and 1,590 predicted coding sequences. Sequence analysis indicates that H. pylori has well-developed systems for motility, for scavenging iron, and for DNA restriction and modification. Many putative adhesins, lipoproteins and other outer membrane proteins were identified, underscoring the potential complexity of host-pathogen interaction. Based on the large number of sequence-related genes encoding outer membrane proteins and the presence of homopolymeric tracts and dinucleotide repeats in coding sequences, H. pylori, like several other mucosal pathogens, probably uses recombination and slipped-strand mispairing within repeats as mechanisms for antigenic variation and adaptive evolution. Consistent with its restricted niche, H. pylori has a few regulatory networks, and a limited metabolic repertoire and biosynthetic capacity. Its survival in acid conditions depends, in part, on its ability to establish a positive inside-membrane potential in low pH." @default.
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- W2110132014 date "1997-08-07" @default.
- W2110132014 modified "2023-10-01" @default.
- W2110132014 title "The complete genome sequence of the gastric pathogen Helicobacter pylori" @default.
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- W2110132014 doi "https://doi.org/10.1038/41483" @default.
- W2110132014 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9252185" @default.
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