Target intelligence / Profile preview

DNA replication licensing factor MCM7 (MCM7)

Target
MCM7
Molecular classification
DNA helicase, DNA replication licensing factor, Cell cycle protein, Enzyme (ATPase activity as part of the helicase complex), Minichromosome maintenance (MCM) protein family
01

Overview

DNA replication licensing factor MCM7 is a highly conserved component of the minichromosome maintenance (MCM) protein family, forming part of the MCM2-7 heterohexameric complex essential for eukaryotic DNA replication initiation and elongation[2][4][6]. MCM7 acts as a DNA helicase, "licensing" DNA replication to ensure the genome is duplicated only once per cell cycle[1][2][6]. The complex assembles at replication origins during G1 phase, and upon S-phase entry, drives replication fork formation by unwinding DNA. MCM7 is tightly regulated, interacting with cell cycle kinases and tumor suppressor proteins, and is essential for cell proliferation, genome stability, and S-phase checkpoint control[2][3][4]. Overexpression is linked to cancer progression and poor prognosis, making MCM7 both a candidate therapeutic target and a biomarker in oncology[3]. No approved drugs currently target MCM7 directly, but its critical role has made it a target of substantial research interest.

Other names
CDC47P1.1-MCM3PPP1R104CDC47 homologP1CDC47P85MCMPNAS146protein phosphatase 1 regulatory subunit 104minichromosome maintenance deficient 7homolog of S. cerevisiae Cdc47
02

Mechanism of action

Not applicable to current drugs; mechanistically, hypothetical drugs could inhibit the helicase activity, disrupt protein-protein interactions within the MCM2-7 complex, or modulate upstream regulators affecting MCM7 expression/function.

03

Biological functions

DNA replication initiationDNA unwinding (helicase activity)Replication fork formation and progressionCell cycle regulation (especially G1/S transition)Genome stability maintenanceS-phase checkpoint activation upon DNA damage
04

Disease associations

Cancer (numerous types; associated with tumorigenesis and prognosis)Other: Potential role in infectious disease susceptibility and host immune response (based on animal models)
05

Safety considerations

Potential toxicity to proliferating normal cells due to the essential role of MCM7 in DNA replication in all dividing cellsRisk of bone marrow suppression, gastrointestinal toxicity, and impaired tissue regeneration if inhibited systemically
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Interacting drugs

None directly approved for clinical use targeting MCM7; no drugs with primary mechanism of action described as direct binding or inhibition/activation of MCM7 in clinical databases as of now.
07

Biomarkers

MCM7 expression level (prognostic biomarker in certain cancers, notably hepatocellular carcinoma; associated with proliferation and patient survival)

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