Evidence map›Paper›PMID 24123256›Full record

ArticleProteins2014

Prediction and validation of the unexplored RNA-binding protein atlas of the human proteome.

Huiying Zhao, Yuedong Yang, Sarath Chandra Janga, C Cheng Kao, Yaoqi Zhou

Open access · bronzeAbstract read
In one paragraph

Article in Proteins, 2014. 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
1.8field-weighted citation impact, top 15% of its field
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, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Sequence-Based Prediction of RNA-Binding Residues in Proteins.Methods in molecular biology (Clifton, N.J.) · 2017
    Article
  10. HOMCOS: an updated server to search and model complex 3D structures.Journal of structural and functional genomics · 2016
    Article
  11. Review
  12. Advances in the characterization of RNA-binding proteins.Wiley interdisciplinary reviews. RNA · 2016
    Review
  13. Article
  14. Template-based prediction of protein function.Current opinion in structural biology · 2015
    Review
  15. Article
  16. 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

5 authors at 2 institutions in 2 countries.

Huiying ZhaoSchool of Informatics and Computing, Indiana University Purdue University, Indianapolis, Indiana, 46202; Center for Computational Biology and Bioinformatics, Indiana University School of Medicine, Indianapolis, Indiana, 46202.
Yuedong Yang
Sarath Chandra Janga
C Cheng Kao
Yaoqi Zhou
Indiana University School of MedicineIndiana University Bloomington · US

Funding

Molecular biology of viral capsidsR01AI090280 · NIAID · TRUSTEES OF INDIANA UNIVERSITY · PI KAO, CHENG C · 2010 to 2013
$1.3M
Statistical Energy Functions: a Fragment-based ApproachR01GM085003 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI ZHOU, YAOQI · 2008 to 2011
$1.1M
NIAID NIH HHS 1R01AI090280NIAID NIH HHS R01 AI090280NIGMS NIH HHS R01 GM085003
6 · The paper itself

Abstract

Detecting protein-RNA interactions is challenging both experimentally and computationally because RNAs are large in number, diverse in cellular location and function, and flexible in structure. As a result, many RNA-binding proteins (RBPs) remain to be identified. Here, a template-based, function-prediction technique SPOT-Seq for RBPs is applied to human proteome and its result is validated by a recent proteomic experimental discovery of 860 mRNA-binding proteins (mRBPs). The coverage (or sensitivity) is 42.6% for 1217 known RBPs annotated in the Gene Ontology and 43.6% for 860 newly discovered human mRBPs. Consistent sensitivity indicates the robust performance of SPOT-Seq for predicting RBPs. More importantly, SPOT-Seq detects 2418 novel RBPs in human proteome, 291 of which were validated by the newly discovered mRBP set. Among 291 validated novel RBPs, 61 are not homologous to any known RBPs. Successful validation of predicted novel RBPs permits us to further analysis of their phenotypic roles in disease pathways. The dataset of 2418 predicted novel RBPs along with confidence levels and complex structures is available at http://sparks-lab.org (in publications) for experimental confirmations and hypothesis generation.

Indexed as

Binding SitesCell Line, TumorDatabases, ProteinDNA-Binding ProteinsHeLa CellsHumansProtein BindingProteomeProteomicsRNA-Binding ProteinsDNA-Binding ProteinsProteomeRNA-Binding ProteinsDNA binding proteinshuman proteomeKEGGRNA binding proteins

Identifiers

PMID24123256
PMCPMC3949140
OpenAlexW2110423360

What OpenQuestion holds

Textmetadata
LicenceTDM
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.