Evidence map›Paper›PMID 21784873›Full record

ArticleGenome research2011

Genome-scale phylogenetic function annotation of large and diverse protein families.

Barbara E Engelhardt, Michael I Jordan, John R Srouji, Steven E Brenner

Abstract read
In one paragraph

Article in Genome research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed, 62 citations in OpenAlex.

  1. Tuning the stator subunit of the flagellar motor with coiled-coil engineering.Protein science : a publication of the Protein Society · 2023
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  12. Computational and Experimental Studies of ADP-Ribosylation.Methods in molecular biology (Clifton, N.J.) · 2017
    Article
  13. PROSNET: INTEGRATING HOMOLOGY WITH MOLECULAR NETWORKS FOR PROTEIN FUNCTION PREDICTION.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2017
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  19. A Bayesian sampler for optimization of protein domain hierarchies.Journal of computational biology : a journal of computational molecular cell biology · 2014
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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

4 authors at 1 institution in 1 country.

Barbara E EngelhardtElectrical Engineering and Computer Science Department, University of California, Berkeley, California 94720, USA. bee@compbio.berkeley.edu
Michael I Jordan
John R Srouji
Steven E Brenner
University of California, Berkeley · US

Funding

Protein function prediction by statistical phylogenomicsR01GM071749 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BRENNER, STEVEN E · 2007 to 2010
$1.4M
COMPUTATIONAL STRUCTURAL AND FUNCTIONAL GENOMICSK22HG000056 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI BRENNER, STEVEN E · 2000 to 2003
$1.1M
NHGRI NIH HHS K22 HG000056NHGRI NIH HHS K22 HG00056NIGMS NIH HHS R01 GM071749
6 · The paper itself

Abstract

The Statistical Inference of Function Through Evolutionary Relationships (SIFTER) framework uses a statistical graphical model that applies phylogenetic principles to automate precise protein function prediction. Here we present a revised approach (SIFTER version 2.0) that enables annotations on a genomic scale. SIFTER 2.0 produces equivalently precise predictions compared to the earlier version on a carefully studied family and on a collection of 100 protein families. We have added an approximation method to SIFTER 2.0 and show a 500-fold improvement in speed with minimal impact on prediction results in the functionally diverse sulfotransferase protein family. On the Nudix protein family, previously inaccessible to the SIFTER framework because of the 66 possible molecular functions, SIFTER achieved 47.4% accuracy on experimental data (where BLAST achieved 34.0%). Finally, we used SIFTER to annotate all of the Schizosaccharomyces pombe proteins with experimental functional characterizations, based on annotations from proteins in 46 fungal genomes. SIFTER precisely predicted molecular function for 45.5% of the characterized proteins in this genome, as compared with four current function prediction methods that precisely predicted function for 62.6%, 30.6%, 6.0%, and 5.7% of these proteins. We use both precision-recall curves and ROC analyses to compare these genome-scale predictions across the different methods and to assess performance on different types of applications. SIFTER 2.0 is capable of predicting protein molecular function for large and functionally diverse protein families using an approximate statistical model, enabling phylogenetics-based protein function prediction for genome-wide analyses. The code for SIFTER and protein family data are available at http://sifter.berkeley.edu.

Indexed as

GenomeMolecular Sequence AnnotationPhylogenyAlgorithmsArylsulfotransferaseComputational BiologyDatabases, ProteinGenome, FungalModels, StatisticalNudix HydrolasesProteinsPyrophosphatasesSchizosaccharomyces pombe ProteinsArylsulfotransferaseNudix HydrolasesProteinsPyrophosphatasesSchizosaccharomyces pombe Proteins

Identifiers

PMID21784873
PMCPMC3205580
OpenAlexW2098127859

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.