Evidence map›Paper›PMID 20807838›Full record

ArticleBioinformatics (Oxford, England)2010

Novel sequence-based method for identifying transcription factor binding sites in prokaryotic genomes.

Gurmukh Sahota, Gary D Stormo

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Global transcriptional regulator TrmB family members in prokaryotes.Journal of microbiology (Seoul, Korea) · 2016
    Review
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  14. Quantifying the sequence-function relation in gene silencing by bacterial small RNAs.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  15. 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

2 authors.

Gurmukh SahotaDepartment of Genetics, Washington University School of Medicine, Saint Louis, MO 63108, USA.
Gary D Stormo

Funding

NATIONAL RESEARCH SERVICE AWARD-MEDICAL SCIENTISTT32GM007200 · NIGMS · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 1985 to 2024
$59.8M
DNA PATTERN IDENTIFICATION AND ANALYSISR01HG000249 · NHGRI · WASHINGTON UNIVERSITY · PI STORMO, GARY D · 1990 to 2017
$5.6M
TRAINING PROGRAM IN COMPUTATIONAL BIOLOGYT32GM008802 · NIGMS · WASHINGTON UNIVERSITY · PI STORMO, GARY D · 2001 to 2010
$1.7M
NHGRI NIH HHS R01 HG000249NHGRI NIH HHS R01 HG00249NIGMS NIH HHS T32 GM007200NIGMS NIH HHS T32 GM008802NIGMS NIH HHS T32 GM07200
6 · The paper itself

Abstract

motivationComputational techniques for microbial genomic sequence analysis are becoming increasingly important. With next-generation sequencing technology and the human microbiome project underway, current sequencing capacity is significantly greater than the speed at which organisms of interest can be studied experimentally. Most related computational work has been focused on sequence assembly, gene annotation and metabolic network reconstruction. We have developed a method that will primarily use available sequence data in order to determine prokaryotic transcription factor (TF) binding specificities.

resultsSpecificity determining residues (critical residues) were identified from crystal structures of DNA-protein complexes and TFs with the same critical residues were grouped into specificity classes. The putative binding regions for each class were defined as the set of promoters for each TF itself (autoregulatory) and the immediately upstream and downstream operons. MEME was used to find putative motifs within each separate class. Tests on the LacI and TetR TF families, using RegulonDB annotated sites, showed the sensitivity of prediction 86% and 80%, respectively. AVAILABILITY: http://ural.wustl.edu/∼gsahota/HTHmotif/

Indexed as

GenomePromoter Regions, GeneticBinding SitesComputational BiologySequence Analysis, DNATranscription FactorsTranscription Factors

Identifiers

PMID20807838
PMCPMC2981494

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.