Evidence map›Paper›PMID 10899148›Full record

ArticleGenome research2000

From complete genomes to measures of substitution rate variability within and between proteins.

N V Grishin, Y I Wolf, E V Koonin

Abstract readComparative Study
In one paragraph

Article in Genome research, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed.

  1. An algorithmic constraint at the transition to complex life.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  7. Loss of quaternary structure is associated with rapid sequence divergence in the OSBS family.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  8. Article
  9. Article
  10. On the number of genomic pacemakers: a geometric approach.Algorithms for molecular biology : AMB · 2014
    Article
  11. Article
  12. Article
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  14. Article
  15. Universal pacemaker of genome evolution.PLoS computational biology · 2012
    Article
  16. Article
  17. Are there laws of genome evolution?PLoS computational biology · 2011
    Article
  18. Article
  19. Article
  20. Review
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

3 authors.

N V GrishinNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894 USA. grishin@chop.swmed.edu
Y I Wolf
E V Koonin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulation of complete genome sequences of diverse organisms creates new possibilities for evolutionary inferences from whole-genome comparisons. In the present study, we analyze the distributions of substitution rates among proteins encoded in 19 complete genomes (the interprotein rate distribution). To estimate these rates, it is necessary to employ another fundamental distribution, that of the substitution rates among sites in proteins (the intraprotein distribution). Using two independent approaches, we show that intraprotein substitution rate variability appears to be significantly greater than generally accepted. This yields more realistic estimates of evolutionary distances from amino-acid sequences, which is critical for evolutionary-tree construction. We demonstrate that the interprotein rate distributions inferred from the genome-to-genome comparisons are similar to each other and can be approximated by a single distribution with a long exponential shoulder. This suggests that a generalized version of the molecular clock hypothesis may be valid on genome scale. We also use the scaling parameter of the obtained interprotein rate distribution to construct a rooted whole-genome phylogeny. The topology of the resulting tree is largely compatible with those of global rRNA-based trees and trees produced by other approaches to genome-wide comparison.

Indexed as

GenomeAmino Acid SubstitutionComputational BiologyEvolution, MolecularGenetic VariationModels, GeneticModels, StatisticalPhylogenyProteinsSequence AlignmentSequence Analysis, ProteinProteins

Identifiers

PMID10899148
PMCPMC310923

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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.