4.8 Article

PHI-base: a new interface and further additions for the multi-species pathogen-host interactions database

Journal

NUCLEIC ACIDS RESEARCH
Volume 45, Issue D1, Pages D604-D610

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkw1089

Keywords

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Funding

  1. UK Biotechnology and Biological Sciences Research Council (BBSRC) [BB/I/001077/1, BB/K020056/1]
  2. BBSRC as a National Capability [BB/J/004383/1]
  3. Research Councils UK Open Access Fund
  4. Biotechnology and Biological Sciences Research Council [BBS/E/C/00005192, BBS/E/C/000I0250, BB/I000488/1, BB/K020056/1, BBS/E/C/00005203] Funding Source: researchfish
  5. BBSRC [BBS/E/C/00005203, BB/K020056/1, BBS/E/C/000I0250, BB/I000488/1, BBS/E/C/00005192] Funding Source: UKRI

Ask authors/readers for more resources

The pathogen-host interactions database (PHI-base) is available at www.phi-base.org. PHI-base contains expertly curated molecular and biological information on genes proven to affect the outcome of pathogen-host interactions reported in peer reviewed research articles. In addition, literature that indicates specific gene alterations that did not affect the disease interaction phenotype are curated to provide complete datasets for comparative purposes. Viruses are not included. Here we describe a revised PHI-base Version 4 data platform with improved search, filtering and extended data display functions. A PHIB-BLAST search function is provided and a link to PHI-Canto, a tool for authors to directly curate their own published data into PHI-base. The new release of PHI-base Version 4.2 (October 2016) has an increased data content containing information from 2219 manually curated references. The data provide information on 4460 genes from 264 pathogens tested on 176 hosts in 8046 interactions. Prokaryotic and eukaryotic pathogens are represented in almost equal numbers. Host species belong similar to 70% to plants and 30% to other species of medical and/or environmental importance. Additional data types included into PHI-base 4 are the direct targets of pathogen effector proteins in experimental and natural host organisms. The curation problems encountered and the future directions of the PHI-base project are briefly discussed.

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