Evidence map›Paper›PMID 31877804›Full record

ArticleMarine drugs2019

Characterization of Nme5-Like Gene/Protein from the Red Alga

Dragutin Perina, Marina Korolija, Andreja Mikoč, Mirna Halasz, Maja Herak Bosnar, Helena Ćetković

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Functional Diversity and Emerging Roles of Human NME/NDPK Group II Proteins.International journal of molecular sciences · 2026
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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

6 authors at 1 institution in 1 country.

Dragutin PerinaDivision of Molecular Biology, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Marina KorolijaDivision of Molecular Medicine, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Andreja MikočDivision of Molecular Biology, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Mirna HalaszDivision of Molecular Biology, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Maja Herak BosnarDivision of Molecular Medicine, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Helena ĆetkovićDivision of Molecular Biology, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Rudjer Boskovic Institute · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Nme gene/protein family of nucleoside diphosphate kinases (NDPK) was originally named after its member Nm23-H1/Nme1, the first identified metastasis suppressor. Human Nme proteins are divided in two groups. They all possess nucleoside diphosphate kinase domain (NDK). Group I (Nme1-Nme4) display a single type NDK domain, whereas Group II (Nme5-Nme9) display a single or several different NDK domains, associated or not associated with extra-domains. Data strongly suggest that, unlike Group I, none of the members of Group II display measurable NDPK activity, although some of them autophosphorylate. The multimeric form is required for the NDPK activity. Group I proteins are known to multimerize, while there are no data on the multimerization of Group II proteins. The Group II ancestral type protein was shown to be conserved in several species from three eukaryotic supergroups. Here, we analysed the Nme protein from an early branching eukaryotic lineage, the red alga

Indexed as

AnimalsCell ProliferationChondrusHEK293 CellsHumansNM23 Nucleoside Diphosphate KinasesNucleoside-Diphosphate KinaseNM23 Nucleoside Diphosphate KinasesNME5 protein, humanNucleoside-Diphosphate KinaseChondrus crispuseukaryotic evolutionNme5Nme evolutionNme gene/protein familyred alga

Identifiers

PMID31877804
PMCPMC7024210
OpenAlexW2994677192

What OpenQuestion holds

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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.