Evidence map›Paper›PMID 19148270›Full record

ArticlePLoS computational biology2009

Partial order optimum likelihood (POOL): maximum likelihood prediction of protein active site residues using 3D Structure and sequence properties.

Wenxu Tong, Ying Wei, Leonel F Murga, Mary Jo Ondrechen, Ronald J Williams

Abstract read
In one paragraph

Article in PLoS computational biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

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41citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

41 citing papers in PubMed.

  1. Article
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  5. MAHOMES II: A webserver for predicting if a metal binding site is enzymatic.Protein science : a publication of the Protein Society · 2023
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  7. Electrostatic fingerprints of catalytically active amino acids in enzymes.Protein science : a publication of the Protein Society · 2022
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  8. Synthesis and Characterization of 5-(2-Fluoro-4-[Journal of medicinal chemistry · 2022
    Article
  9. Article
  10. Article
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  12. Article
  13. Machine learning for enzyme engineering, selection and design.Protein engineering, design & selection : PEDS · 2021
    Review
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  15. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Wenxu TongCollege of Computer and Information Science, Northeastern University, Boston, Massachusetts, United States of America.
Ying Wei
Leonel F Murga
Mary Jo Ondrechen
Ronald J Williams

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A new monotonicity-constrained maximum likelihood approach, called Partial Order Optimum Likelihood (POOL), is presented and applied to the problem of functional site prediction in protein 3D structures, an important current challenge in genomics. The input consists of electrostatic and geometric properties derived from the 3D structure of the query protein alone. Sequence-based conservation information, where available, may also be incorporated. Electrostatics features from THEMATICS are combined with multidimensional isotonic regression to form maximum likelihood estimates of probabilities that specific residues belong to an active site. This allows likelihood ranking of all ionizable residues in a given protein based on THEMATICS features. The corresponding ROC curves and statistical significance tests demonstrate that this method outperforms prior THEMATICS-based methods, which in turn have been shown previously to outperform other 3D-structure-based methods for identifying active site residues. Then it is shown that the addition of one simple geometric property, the size rank of the cleft in which a given residue is contained, yields improved performance. Extension of the method to include predictions of non-ionizable residues is achieved through the introduction of environment variables. This extension results in even better performance than THEMATICS alone and constitutes to date the best functional site predictor based on 3D structure only, achieving nearly the same level of performance as methods that use both 3D structure and sequence alignment data. Finally, the method also easily incorporates such sequence alignment data, and when this information is included, the resulting method is shown to outperform the best current methods using any combination of sequence alignments and 3D structures. Included is an analysis demonstrating that when THEMATICS features, cleft size rank, and alignment-based conservation scores are used individually or in combination THEMATICS features represent the single most important component of such classifiers.

Indexed as

Catalytic DomainModels, MolecularAmino Acid SequenceAnimalsConserved SequenceGenomicsHumansLikelihood FunctionsModels, ChemicalProtein FoldingProteinsProtein Structure, SecondaryROC CurveSequence AlignmentSequence Analysis, ProteinStatic ElectricityProteins

Identifiers

PMID19148270
PMCPMC2612599

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.