Evidence map›Paper›PMID 15498934›Full record

ArticleProtein science : a publication of the Protein Society2004

Predicting enzyme family class in a hybridization space.

Kuo-Chen Chou, Yu-Dong Cai

Abstract read
In one paragraph

Article in Protein science : a publication of the Protein Society, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  13. Molecular biocoding of insulin.Advances and applications in bioinformatics and chemistry : AABC · 2010
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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

2 authors.

Kuo-Chen ChouGordon Life Science Institute, San Diego, CA 92130, USA. kchou@san.rr.com
Yu-Dong Cai

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Given the sequence of a protein, how can we predict whether it is an enzyme or a non-enzyme? If it is, what enzyme family class it belongs to? Because these questions are closely relevant to the biological function of a protein and its acting object, their importance is self-evident. Particularly with the explosion of protein sequences entering into data banks and the relatively much slower progress in using biochemical experiments to determine their functions, it is highly desired to develop an automated method that can be used to give fast answers to these questions. By hybridizing the gene ontology and pseudo-amino-acid composition, we have introduced a new method that is called GO-PseAA predictor and operate it in a hybridization space. To avoid redundancy and bias, demonstrations were performed on a data set in which none of the proteins in an individual class has > or =40% sequence identity to any other. The overall success rate thus obtained by the jackknife cross-validation test in identifying enzyme and non-enzyme was 93%, and that in identifying the enzyme family was 94% for the following six main Enzyme Commission (EC) classes: (1) oxidoreductase, (2) transferase, (3) hydrolase, (4) lyase, (5) isomerase, and (6) ligase. The corresponding rates by the independent data set test were 98% and 97%, respectively.

Indexed as

Amino Acid SequenceModels, TheoreticalEnzymesModels, MolecularProteomicsEnzymes

Identifiers

PMID15498934
PMCPMC2286574

What OpenQuestion holds

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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.