Evidence map›Paper›PMID 23421754›Full record

ArticleInorganic chemistry2013

Macrocyclization of the ATCUN motif controls metal binding and catalysis.

Kosh P Neupane, Amanda R Aldous, Joshua A Kritzer

Abstract read
In one paragraph

Article in Inorganic chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. DNA Scission by Non-Histidine Amino-Terminal Cu(II) and Ni(II) Binding-Like Peptides.Chembiochem : a European journal of chemical biology · 2026
    Article
  2. Inorganic chemistry · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. The effect of an engineered ATCUN motif on the structure and biophysical properties of the SH3 domain of c-Src tyrosine kinase.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2020
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. 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

3 authors.

Kosh P NeupaneDepartment of Chemistry, Tufts University, 62 Talbot Avenue, Medford, Massachusetts 02155, United States.
Amanda R Aldous
Joshua A Kritzer

Funding

Rapid Generation of Isoform-Selective Histone Deacetylase InhibitorsR21AG038776 · NIA · TUFTS UNIVERSITY MEDFORD · PI KRITZER, JOSHUA A · 2011 to 2012
$349k
NIA NIH HHS R21 AG038776NIA NIH HHS R21AG038776
6 · The paper itself

Abstract

We report the design, synthesis, and characterization of macrocyclic analogues of the amino-terminal copper and nickel binding (ATCUN) motif. These macrocycles have altered pH transitions for metal binding, and unlike linear ATCUN motifs, the optimal cyclic peptide 1 binds Cu(II) selectively over Ni(II) at physiological pH. UV-vis and EPR spectroscopy showed that cyclic peptide 1 can coordinate Cu(II) or Ni(II) in a square planar geometry. Metal binding titration and ESI-MS data revealed a 1:1 binding stoichiometry. Macrocyclization allows for coordination of Cu(II) or Ni(II) as in linear ATCUN motifs, but with enhanced DNA cleavage by the Cu(II)-1 complex relative to linear analogues. The Cu(II)-1 complex was also capable of producing diffusible hydroxyl radicals, which is unique among ATCUN motifs and most other common copper(II) chelators.

Indexed as

Binding SitesCatalysisCopperCyclizationHydrogen-Ion ConcentrationMacrocyclic CompoundsModels, MolecularMolecular StructureNickelOrganometallic CompoundsPeptides, CyclicCopperMacrocyclic CompoundsNickelOrganometallic CompoundsPeptides, Cyclic

Identifiers

PMID23421754
PMCPMC3603286

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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.