TrpNet

TrpNet maps and predicts tryptophan metabolism within host-gut microbiome interactions to characterize metabolites, enzymes, and reactions across human and mouse gut bacteria.


Key Features:

  • Extensive database: Contains data on 130 reactions, 108 metabolites, and 91 enzymes across 1246 human gut bacterial species and 88 mouse gut bacterial species.
  • Predictive analytics: Employs a Bayesian logistic regression model to predict potential tryptophan metabolites from gut microbiome taxonomy profiles.
  • Host–microbiome co-metabolic mapping: Represents co-metabolic processes between hosts (humans and mice) and their gut microbiota related to tryptophan biotransformation.
  • Validation and efficacy: Validated using two gut microbiome metabolomics studies and demonstrated superior performance in predicting alterations in indole derivatives compared to other established methods.

Scientific Applications:

  • Pathway elucidation: Characterizes pathways by which tryptophan is metabolized into microbial and host-associated metabolites.
  • Immune modulation studies: Enables investigation of tryptophan-derived metabolites that modulate immune responses.
  • Metabolic and neuronal function research: Supports analysis of metabolites implicated in metabolic functions and neuronal activities locally in the gut and at distant sites.
  • Development, health, and disease research: Facilitates studies of animal development, health, and disease states influenced by host–microbiome tryptophan metabolism.

Methodology:

Uses a Bayesian logistic regression model to predict tryptophan metabolites from gut microbiome taxonomy profiles and validation was performed using two gut microbiome metabolomics studies.

Topics

Details

Cost:
Free of charge
Tool Type:
web application
Operating Systems:
Mac, Linux, Windows
Added:
6/8/2022
Last Updated:
6/8/2022

Operations

Publications

Lu Y, Chong J, Shen S, Chammas J, Chalifour L, Xia J. TrpNet: Understanding Tryptophan Metabolism across Gut Microbiome. Metabolites. 2021;12(1):10. doi:10.3390/metabo12010010. PMID:35050132. PMCID:PMC8777792.