Evidence map›Paper›PMID 7651832›Full record

ReviewNucleic acids research1995

Evolution of the SNF2 family of proteins: subfamilies with distinct sequences and functions.

J A Eisen, K S Sweder, P C Hanawalt

Open access · bronzeAbstract readReview
In one paragraph

Review in Nucleic acids research, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 301 papers.

0numbers the graph read from it
0cells of the map it votes in
301citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

301 citing papers in PubMed, 711 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. CHD1L in cancer and beyond: structure, oncogenic functions, and therapeutic potential.Journal of experimental & clinical cancer research : CR · 2025
    Review
  5. Article
  6. Review
  7. How does CHD4 slide nucleosomes?Biochemical Society transactions · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Biophysics of Chromatin Remodeling.Annual review of biophysics · 2021
    Review
  19. Review
  20. Review

241 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

J A EisenDepartment of Biological Sciences, Stanford University, CA 94305-5020, USA.
K S Sweder
P C Hanawalt
Stanford University · US

Funding

Postgraduate Training Program in Epithelial BiologyT32AR007422 · NIAMS · STANFORD UNIVERSITY · PI PAUL KHAVARI · 1986 to 2026
$5.0M
CELULAR PROCESSING OF DAMAGED DNA--ROLE IN ONCOGENESISR35CA044349 · NCI · STANFORD UNIVERSITY · PI HANAWALT, PHILIP C · 1987 to 2000
$959k
NCI NIH HHS CA44349NIAMS NIH HHS T32AR07422
6 · The paper itself

Abstract

The SNF2 family of proteins includes representatives from a variety of species with roles in cellular processes such as transcriptional regulation (e.g. MOT1, SNF2 and BRM), maintenance of chromosome stability during mitosis (e.g. lodestar) and various aspects of processing of DNA damage, including nucleotide excision repair (e.g. RAD16 and ERCC6), recombinational pathways (e.g. RAD54) and post-replication daughter strand gap repair (e.g. RAD5). This family also includes many proteins with no known function. To better characterize this family of proteins we have used molecular phylogenetic techniques to infer evolutionary relationships among the family members. We have divided the SNF2 family into multiple subfamilies, each of which represents what we propose to be a functionally and evolutionarily distinct group. We have then used the subfamily structure to predict the functions of some of the uncharacterized proteins in the SNF2 family. We discuss possible implications of this evolutionary analysis on the general properties and evolution of the SNF2 family.

Indexed as

Biological EvolutionNuclear ProteinsAmino Acid SequenceAnimalsConserved SequenceDNA-Binding ProteinsDNA HelicasesHumansMolecular Sequence DataPhylogenySequence AlignmentSequence Homology, Amino AcidSoftwareTranscription FactorsDNA-Binding ProteinsDNA HelicasesNuclear ProteinsSMARCA1 protein, humanSMARCA2 protein, humanSMARCA4 protein, humanTranscription Factors

Identifiers

PMID7651832
PMCPMC307096
OpenAlexW1990586926

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.