Published April 2, 2024 | Version 1.1

Full-length and split homologs of human proteins in the gut microbiome

  • 1. ROR icon The Ohio State University
  • 2. University of California San Francisco

Contributors

Project leader:

  • 1. ROR icon The Ohio State University
  • 2. University of California San Francisco

Description

These files were generated as part of the manuscript "Human xenobiotic metabolism proteins have full-length and split homologs in the gut microbiome" (submitted).

The .tar file contains .ipc files that are tables of full-length (full_humcover3.ipc) and split homologs (part_humcover3.ipc) of human proteins in the gut microbiome, organized by alignment coverage threshold. For example, the directory `HumanUPR_0.67_src_20000_70` contains results obtained at a 67% alignment coverage threshold for the bacterial protein, and 70% for the human protein. Note that our pipeline collapses full-length alignments to the same UHGP-90 protein family into a single entry per species, with the number of genomes reported in the column nGenomes. Split homologs are not collapsed because genomic context is used to define them, and this context may differ across individual genomes.

These files are in Arrow IPC format, which provides compression and fast I/O for large tables. We recommend reading them using pola.rs or the R Arrow package. In particular, because the full-length homolog table is large, you may wish to work with it without loading it into memory, which can be accomplished using scan_ipc in pola.rs or open_dataset in R Arrow.

We also provide gzipped .csv format datasets of full-length (pgkb_FH_drugs.csv.gz) and split (pgkb_SH_drugs.csv.gz) homologs, at the default 67% alignment coverage threshold for bacterial and 70% for human proteins, organized by their PharmGKB annotations. For each drug annotated in PharmGKB as being metabolized by a human protein with full-length or split homologs, we provide the human protein(s) responsible, its xenobiotic enzyme class, the bacterial protein homolog(s), length and percent identity of the alignment, and either the specific genome (g, split homologs only) or the number of genomes (nGenomes, full homologs only). Xenobiotic enzyme classes are defined as in Figure 4 of the manuscript, with the additional classes "nucl" (nucleobase-containing metabolic proteins not annotated to any other class), "redox" (oxidoreductases not annotated to any other class), and "other" (all remaining proteins).

Files

Files (12.2 GB)

Name Size
md5:51f3a90446c5bc617f6ffea5babbde6e
12.2 GB Download
md5:04515c7c9b052410ea313c084b27258d
2.5 MB Download
md5:eb7d95dde65ac57b064cdeb41a2dce60
61.1 kB Download

Additional details

Funding

National Institutes of Health
Interrogating function, regulation, and interactions in a clade of prevalent human gut microbes R35GM151155
National Institutes of Health
Metabolism of cancer chemotherapeutics by the human gut microbiome R01CA255116
National Institutes of Health
Predicting and preventing drug metabolism by the human gut microbiome R01HL122593

Dates

Submitted
2025-04-02

Software

Repository URL
https://github.com/pbradleylab/split_homology
Programming language
Python , R