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Moghe, G.

Publications and source records attributed to Moghe, G..

2 recordsLinked to original sources

FuncFetch: An LLM-assisted workflow enables mining thousands of enzyme-substrate interactions from published manuscripts

MotivationThousands of genomes are publicly available, however, most genes in those genomes have poorly defined functions. This is partly due to a gap between previously published, experimentally-characterized protein activities and activities deposited in databases. This activity deposition is bottlenecked by the time-consuming biocuration process. The emergence of large language models (LLMs) presents an opportunity to speed up text-mining of protein activities for biocuration. ResultsWe developed FuncFetch -- a workflow that integrates NCBI E-Utilities, OpenAIs GPT-4 and Zotero -- to screen thousands of manuscripts and extract enzyme activities. Extensive validation revealed high precision and recall of GPT-4 in determining whether the abstract of a given paper indicates presence of a characterized enzyme activity in that paper. Provided the manuscript, FuncFetch extracted data such as species information, enzyme names, sequence identifiers, substrates and products, which were subjected to extensive quality analyses. Comparison of this workflow against a manually curated dataset of BAHD acyltransferase activities demonstrated a precision/recall of 0.86/0.64 in extracting substrates. We further deployed FuncFetch on nine large plant enzyme families. Screening 27,120 papers, FuncFetch retrieved 32,605 entries from 5547 selected papers. We also identified multiple extraction errors including incorrect associations, non-target enzymes, and hallucinations, which highlight the need for further manual curation. The BAHD activities were verified, resulting in a comprehensive functional fingerprint of this family and revealing that [~]70% of the experimentally characterized enzymes are uncurated in the public domain. FuncFetch represents an advance in biocuration and lays the groundwork for predicting functions of uncharacterized enzymes. Availability and ImplementationCode and minimally-curated activities available at: https://github.com/moghelab/funcfetch and https://tools.moghelab.org/funczymedb

bioinformatics↗

metaPathwayMap: A tool to predict metabolic pathway neighborhoods from structural classes of untargeted metabolomics peaks

SummaryThousands of peaks detected via untargeted tandem liquid chromatography mass spectrometry (LC-MS/MS) of natural extracts typically go unannotated, limiting our understanding of the metabolic pathways perturbed under different conditions. Current tools for predicting metabolic pathways from untargeted metabolomics data either require prior compound identification or are more focused on specific model species. metaPathwayMap makes use of recent advances in computational metabolomics to map peaks detected in untargeted LC-MS/MS experiments to MetaCyc pathway representations using their structural class predictions. This approach enables better insights into metabolomes of model and non-model species. Availability and ImplementationRequired Python scripts can be downloaded from the moghelab/metaPathwayMap GitHub repository and implemented on a Unix machine. This tool is also available for use through the SolCyc website (https://metapathwaymap.solgenomics.net) and via DockerHub (srs57/metapathwaymap). Contactgdm67@cornell.edu Supplementary InformationAdditional information is provided in Supplementary Methods, Supplementary Files 1-3 and on GitHub (https://github.com/moghelab/metaPathwayMap)

bioinformatics↗