Target intelligence / Profile preview

NIMA-related kinase 5 (NEK5)

Target
NEK5
Molecular classification
Enzyme, Serine/threonine-protein kinase, Protein kinase, NIMA (never in mitosis gene a)-related kinase family
01

Overview

NIMA-related kinase 5 (NEK5) is a member of the NIMA (never in mitosis gene a)-related serine/threonine protein kinase family, which plays important roles in cell cycle regulation and mitosis[1][3]. NEK5 is characterized structurally by a unique DEAD-box domain and acts predominantly in regulating centrosome and cell cycle integrity, as well as chromatin remodeling[1][2][3]. It is predicted to participate in cysteine-type endopeptidase regulation and muscle cell differentiation[2]. Increased expression or aberrant function of NEK5 has been associated with multiple solid tumor types, including breast, lung, prostate, and nasopharyngeal cancer, and is linked to poor prognosis[1]. RNA and protein profiling studies have described its upregulation as a potential marker and therapeutic target in cancer, although most evidence comes from genomics and transcriptomics analyses, with limited direct experimental validation[1]. NEK5 is considered a potential therapeutic target for novel kinase inhibitors, but to date, no approved drugs specifically modulate its function, and its physiological and safety profiles remain incompletely characterized[3].

Other names
Serine/threonine-protein kinase Nek5NimA-related protein kinase 5Never in mitosis A-related kinase 5NIMA (never in mitosis gene a)-related kinase 5NEK5
02

Mechanism of action

Inhibition of serine/threonine kinase activity (by small molecule inhibitors, experimental)[3]

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Biological functions

Cell cycle regulationRegulation of centrosome integrityChromatin remodelingMuscle cell differentiationPositive regulation of cysteine-type endopeptidase activityDNA damage responseSignal transduction
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Disease associations

CancerBardet-Biedl syndrome (association suggested)
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Safety considerations

Potential for off-target effects due to homology with other kinases (the kinase family is highly conserved)[3]Unclear physiological consequences of systemic NEK5 inhibition (not fully explored in vivo or in clinical studies)[1]
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Interacting drugs

No clinically validated drugs, but kinase inhibitor screens (e.g., Davis MI et al., 2011) have identified experimental small molecule inhibitors that target NEK5’s kinase domain[3]
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Biomarkers

Increased NEK5 mRNA/protein as a biomarker of poor prognosis in several cancers (such as breast cancer and prostate cancer, by RNA/proteomic profiling)[1]NEK5 RNA as a putative biomarker in prostate cancer tissue sequencing studies[1]

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