Evidence map›Paper›PMID 20438647›Full record

ArticleBMC bioinformatics2010

SeqRate: sequence-based protein folding type classification and rates prediction.

Guan Ning Lin, Zheng Wang, Dong Xu, Jianlin Cheng

Abstract read
In one paragraph

Article in BMC bioinformatics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. 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

4 authors.

Guan Ning LinInformatics Institute, University of Missouri, Columbia, 65211, USA. guanlin@mail.missouri.edu
Zheng Wang
Dong Xu
Jianlin Cheng

Funding

New Scoring, Assembly and Evaulation Techiniques for Protein Structure PredictionR33GM078601 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI XU, DONG · 2008 to 2010
$659k
NIGMS NIH HHS 1R33GM078601
6 · The paper itself

Abstract

backgroundProtein folding rate is an important property of a protein. Predicting protein folding rate is useful for understanding protein folding process and guiding protein design. Most previous methods of predicting protein folding rate require the tertiary structure of a protein as an input. And most methods do not distinguish the different kinetic nature (two-state folding or multi-state folding) of the proteins. Here we developed a method, SeqRate, to predict both protein folding kinetic type (two-state versus multi-state) and real-value folding rate using sequence length, amino acid composition, contact order, contact number, and secondary structure information predicted from only protein sequence with support vector machines.

resultsWe systematically studied the contributions of individual features to folding rate prediction. On a standard benchmark dataset, the accuracy of folding kinetic type classification is 80%. The Pearson correlation coefficient and the mean absolute difference between predicted and experimental folding rates (sec-1) in the base-10 logarithmic scale are 0.81 and 0.79 for two-state protein folders, and 0.80 and 0.68 for three-state protein folders. SeqRate is the first sequence-based method for protein folding type classification and its accuracy of fold rate prediction is improved over previous sequence-based methods. Its performance can be further enhanced with additional information, such as structure-based geometric contacts, as inputs.

conclusionsBoth the web server and software of predicting folding rate are publicly available at http://casp.rnet.missouri.edu/fold_rate/index.html.

Indexed as

Artificial IntelligenceProtein FoldingAlgorithmsAmino AcidsAmino Acid SequenceComputational BiologyInternetKineticsLinear ModelsProtein ConformationProteinsReproducibility of ResultsSequence Analysis, ProteinSoftwareAmino AcidsProteins

Identifiers

PMID20438647
PMCPMC2863059

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.