Target intelligence / Profile preview

Dynein axonemal assembly factor 15 (PIH1D2)

Target
PIH1D2
Molecular classification
Other (Co-chaperone/cofactor for multiprotein assembly complexes), Axonemal dynein assembly factor, Component of the R2TP complex
01

Overview

Dynein axonemal assembly factor 15 (PIH1D2) is a member of the PIH1 domain–containing protein family, serving as a co-chaperone/co-factor in the preassembly of axonemal dynein arms, which are essential for the movement of motile cilia[2]. PIH1D2 functions primarily in the cytoplasm and is a component of the R2TP complex, interacting with molecular chaperones such as Hsp90 to assist in the assembly and stabilization of large macromolecular complexes[1]. Its PIH1 domain facilitates phosphorylation-dependent protein-protein interactions, particularly with phosphoserine-containing motifs, and it is implicated in the assembly of ribonucleoprotein particles, RNA polymerase complexes, and chromatin remodeling. In vertebrates, PIH1D2 is required for proper assembly of dynein motors within cilia; loss of function can result in impaired ciliary motility and contribute to disorders such as primary ciliary dyskinesia[2]. Unlike many classical drug targets (e.g., receptors, enzymes), there are currently no known drugs or direct mechanisms of small-molecule action targeting PIH1D2, nor is it established as a selective therapeutic biomarker or a recognized target for pharmaceutical intervention.

Other names
PIH1 domain-containing protein 2PIH1D2DNAAF15PIH1 domain containing 2dynein axonemal assembly factor 15
02

Biological functions

Ciliary dynein preassemblyProtein-protein interactions (phosphopeptide binding)Association with Hsp90 chaperone systemInvolved in complex assembly (e.g. ribonucleoproteins, RNA polymerase I preinitiation complex)Regulation of protein localization to chromatinChromatin remodeling
03

Disease associations

Primary ciliary dyskinesia (defective motile cilia function)[2]Other ciliopathies

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