Evidence map›Paper›PMID 35724564›Full record

ArticleBriefings in bioinformatics2022

PCfun: a hybrid computational framework for systematic characterization of protein complex function.

Varun S Sharma, Andrea Fossati, Rodolfo Ciuffa, Marija Buljan, Evan G Williams, Zhen Chen, Wenguang Shao, Patrick G A Pedrioli, Anthony W Purcell, María Rodríguez Martínez and 4 more

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Varun S SharmaDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Switzerland.
Andrea FossatiQuantitative Biosciences Institute (QBI) and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, CA 94158, USA.
Rodolfo CiuffaDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Switzerland.
Marija BuljanEmpa - Swiss Federal Laboratories for Materials Science and Technology, St. Gallen, Switzerland.
Evan G WilliamsLuxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette Luxembourg.
Zhen ChenCollaborative Innovation Center of Henan Grain Crops, Henan Agricultural University, Zhengzhou 450046, China.
Wenguang ShaoDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Switzerland.
Patrick G A PedrioliDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Switzerland.
Anthony W PurcellMonash Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC 3800, Australia.
María Rodríguez MartínezIBM Research Europe, Zurich, Switzerland.
Jiangning SongMonash Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC 3800, Australia.ORCID 0000-0001-8031-9086
Matteo ManicaIBM Research Europe, Zurich, Switzerland.ORCID 0000-0002-8872-0269
Ruedi AebersoldDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Switzerland.
Chen LiDepartment of Biology, Institute of Molecular Systems Biology, ETH Zurich, Switzerland.ORCID 0000-0002-1847-754X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In molecular biology, it is a general assumption that the ensemble of expressed molecules, their activities and interactions determine biological function, cellular states and phenotypes. Stable protein complexes-or macromolecular machines-are, in turn, the key functional entities mediating and modulating most biological processes. Although identifying protein complexes and their subunit composition can now be done inexpensively and at scale, determining their function remains challenging and labor intensive. This study describes Protein Complex Function predictor (PCfun), the first computational framework for the systematic annotation of protein complex functions using Gene Ontology (GO) terms. PCfun is built upon a word embedding using natural language processing techniques based on 1 million open access PubMed Central articles. Specifically, PCfun leverages two approaches for accurately identifying protein complex function, including: (i) an unsupervised approach that obtains the nearest neighbor (NN) GO term word vectors for a protein complex query vector and (ii) a supervised approach using Random Forest (RF) models trained specifically for recovering the GO terms of protein complex queries described in the CORUM protein complex database. PCfun consolidates both approaches by performing a hypergeometric statistical test to enrich the top NN GO terms within the child terms of the GO terms predicted by the RF models. The documentation and implementation of the PCfun package are available at https://github.com/sharmavaruns/PCfun. We anticipate that PCfun will serve as a useful tool and novel paradigm for the large-scale characterization of protein complex function.

Indexed as

Computational BiologyProteinsDatabases, ProteinGene OntologyHumansNatural Language ProcessingProteinsgene ontologymachine learningnatural language processingprotein complex function

Identifiers

PMID35724564
PMCPMC9310514

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.