Evidence map›Paper›PMID 20437037›Full record

ArticleJournal of molecular evolution2010

Circadian input kinases and their homologs in cyanobacteria: evolutionary constraints versus architectural diversification.

Ivan Baca, Daniel Sprockett, Volodymyr Dvornyk

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Article in Journal of molecular evolution, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

The trial behind it

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
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  3. Review
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  7. Review
  8. Single mutations in sasA enable a simpler ΔcikA gene network architecture with equivalent circadian properties.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
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  12. Review
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ivan BacaInstitute of Genetics, National Academy of Sciences of Moldova, Chisinau, Moldova. bidmd@yahoo.com
Daniel Sprockett
Volodymyr Dvornyk

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The circadian input kinase A (cikA) gene encodes a protein relaying environmental signal to the central circadian oscillator in cyanobacteria. The CikA protein has a variable architecture and usually consists of four tandemly arrayed domains: GAF, histidine kinase (HisKA), histidine kinase-like ATPase (HATPase_c), and a pseudo-receiver (REC). Among them, HisKA and HATPase_c are the least polymorphic, and REC is not present in heterocystic filamentous cyanobacteria. CikA contains several conserved motifs that are likely important for circadian function. There are at least three types of circadian systems, each of which possesses a different set of circadian genes. The originally described circadian system (kaiABC system) possesses both cikA and kaiA, while the others lack either only cikA (kaiABC (Delta)) or both (kaiBC). The results we obtained allowed us to approximate the time of the cikA origin to be about 2600-2200 MYA and the time of its loss in the species with the kaiABC (Delta) or kaiBC system between 1100 and 600 MYA. Circadian specialization of CikA, as opposed to its non-circadian homologs, is a result of several factors, including the unique conserved domain architecture and high evolutionary constraints of some domains and regions, which were previously identified as critical for the circadian function of the gene.

Indexed as

Evolution, MolecularAmino Acid SequenceAnalysis of VarianceBacterial ProteinsBayes TheoremCyanobacteriaDatabases, GeneticMolecular Sequence DataPhylogenyPoint MutationProtein KinasesSequence AlignmentSequence Homology, Amino AcidBacterial ProteinsCikA protein, bacteriaProtein Kinases

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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.