ReviewInternational journal of molecular sciences2026
Functional Diversity and Emerging Roles of Human NME/NDPK Group II Proteins.
Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
NME/NDP kinases are enzymes primarily responsible for maintaining nucleotide balance in the cell. They arose early in evolution, during which they acquired additional biochemical and biological functions such as protein histidine kinase activity, DNA transcription and repair, and the binding and transfer of phospholipids. The human NME/NDPK family comprises 10 proteins divided into two groups. The well-documented Group I (NME1-4) is characterized by high sequence homology and a single active NDPK domain. In contrast, the remaining NME genes/proteins belong to the poorly understood and more heterogeneous Group II. They possess one or more NDPK domains and are divergent in their amino acid sequences. Except for NME6, they have been considered enzymatically inactive. In recent years, NME Group II proteins have attracted more interest from researchers, and new emerging evidence may change the established perspective.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.