Target intelligence / Profile preview

Protein phosphatase 4 regulatory subunit 3B (PPP4R3B)

Target
PPP4R3B
Molecular classification
Regulatory subunit, Protein phosphatase complex component, Other
01

Overview

Protein phosphatase 4 regulatory subunit 3B (PPP4R3B) is a regulatory subunit of the serine/threonine-protein phosphatase 4 (PP4) complex[5][4], which participates in the regulation of cellular protein dephosphorylation processes. PPP4R3B forms heterotrimeric complexes with PP4C (the catalytic subunit) and other regulatory subunits (such as PP4R2)[3]. It is involved in the regulation of double-strand break repair and DNA damage response—critical for maintaining genomic stability—by influencing the activity and substrate specificity of the PP4 phosphatase complex[4][1][3]. PPP4R3B localizes to the nucleus, centrosome, and chromatin[4][5]. While gene-disease association data link PPP4R3B to several inherited conditions (such as sarcosinemia and intracranial abscess), it is not currently known as a direct drug target nor are there any drugs with established mechanisms acting upon it[4]. PPP4R3B, as part of the PP4 complex, plays a crucial biological function in response to DNA damage, and its dysregulation can have significant effects on cell cycle, DNA repair, and possibly tumorigenesis[3][4].

Other names
SMEK2KIAA1387PSY2FLFL2FLJ31474SMEK homolog 2suppressor of mek1smk1
02

Biological functions

Regulation of double-strand break (DSB) DNA repair[1][4]Protein phosphatase activator activity (regulation of PPP4C, the catalytic PP4 subunit)[5][4]Genomic stability maintenance[3]Involvement in DNA damage response (DDR)[1][3][4]Cell cycle regulation (especially during mitosis)[3]
03

Disease associations

Cancer (by implication through genomic instability and DNA repair defects)[3][4]Neurodevelopmental, potentially involved in neuronal development (based on PP4 roles)[3]Other (sarcosinemia, intracranial abscess are gene-level associations but not established therapeutic targeting)[4]
04

Safety considerations

Potential genomic instability if dysregulated[3]Off-target effects related to broad PP4 complex functions

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