Evidence map›Paper›PMID 15696373›Full record

ArticleJournal of molecular evolution2005

Molecular evolution of ldpA, a gene mediating the circadian input signal in cyanobacteria.

Volodymyr Dvornyk

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Article in Journal of molecular evolution, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

5 citing papers in PubMed.

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4 · The record

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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

1 author.

Volodymyr DvornykOsteoporosis Research Center and Department of Biomedical Sciences, Creighton University, 601 North 30th Street, Suite 6730, Omaha, NE 68131, USA. dvornyk@creighton.edu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ldpA gene is an element of the cyanobacterial circadian system and mediates input to the clock. Using complete prokaryotic genomes from various public databases, I analyzed the structure and phylogeny of the ldpA genes. This gene belongs to the large superfamily of ferredoxins and has a HycB domain as a core element of its structure. In addition to this domain, ldpA has two conserved terminal domains that are specific to this gene and have no homologs in the databases. All three domains are under different selective constraints. The ldpA tree topology features two very distinct clades that are essentially the same as those in the previously reported trees of the sasA gene and the kaiBC operon, two other elements of the circadian system. The data on the ldpA polymorphism and evolutionary patterns give further support to the existence of two types of the system, kaiABC- and kaiBC-based, respectively. Each type has specific functional and selective constraints, which have likely been attained through highly concordant evolution of the system's components.

Indexed as

Evolution, MolecularAmino Acid SequenceBacterial ProteinsBinding SitesCircadian RhythmCyanobacteriaIron-Sulfur ProteinsModels, GeneticMolecular Sequence DataPolymorphism, GeneticSelection, GeneticSequence AlignmentSequence Homology, Amino AcidSignal TransductionBacterial ProteinsIron-Sulfur Proteins

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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.