Target intelligence / Profile preview

Yip1 interacting factor homolog A, membrane trafficking protein (YIF1A)

Target
YIF1A
Molecular classification
Transmembrane protein, Membrane trafficking protein, Predicted transporter, Associated with the Yip1 domain family (YIPF proteins), Sometimes conceptualized as a candidate channel, transporter, or transmembrane receptor
01

Overview

Yip1 interacting factor homolog A (YIF1A) is a multi-span transmembrane protein localized primarily to the Golgi apparatus and ER-Golgi intermediate compartment, encoded by the YIF1A gene on chromosome 11. It is a member of the Yip1 domain family (YIPF proteins), which have essential roles across eukaryotes. YIF1A forms complexes with related proteins and functions primarily in ER to Golgi transport, vesicle budding, and fusion, acting in protein trafficking and maintaining Golgi structure. It interacts with COPII vesicle components (Sec23, Sec24), Rab GTPases, and other trafficking regulators. Studies implicate it in cellular stress adaptation (UPR/ER stress), survival pathways in cancer, and neurodegeneration, with specific disease associations including ALS8, Schuurs-Hoeijmakers syndrome, Alzheimer's disease, bipolar disorder, and certain myopathies. Knockdown results in Golgi fragmentation and trafficking disruption, and it is required for IRE1 and PERK activation in ER stress response pathways. While it is not a present drug target, its central role in cell trafficking and disease makes it a candidate for therapeutic exploration.

Other names
YIF1AYIF1YIF1P54TMFinGER754TMpYip1p-interacting factorYIP1-interacting factor homolog A
02

Mechanism of action

Not established for drugs targeting YIF1A; functions are inferred from its biological roles in trafficking, stress response, and potential interaction networks

03

Biological functions

Endoplasmic reticulum (ER) to Golgi vesicle-mediated transportVesicle budding and fusion regulationMembrane delivery and protein trafficking within the secretory pathwayInteraction with COPII vesicle components and Rab GTPasesRegulation of unfolded protein response (UPR)/ER stressGolgi apparatus structure maintenancePossible dendrite pruning in neuronal development
04

Disease associations

Amyotrophic lateral sclerosis type 8Alzheimer diseaseSchuurs-Hoeijmakers syndromeBreast cancerBipolar disorderInfection (e.g., Brucella)Plasma fibronectin deficiency, metabolic myopathies
05

Safety considerations

No direct safety concerns described in the context of therapeutic targeting; risks would likely involve disruption of vesicle trafficking and ER-Golgi communication, affecting protein secretion and cell viability

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