Target intelligence / Profile preview

Keratin, type II cytoskeletal 1 (KRT1)

Target
KRT1
Molecular classification
Intermediate filament protein, Type II keratin, Cytoskeletal protein
01

Overview

Keratin, type II cytoskeletal 1 (KRT1), is a **major type II intermediate filament protein** expressed predominantly in the suprabasal layers of the epidermis, where it forms heterodimers with keratin 10 or keratin 9 to create the intermediate filament cytoskeleton essential for skin integrity and barrier function[1][2][3][5]. KRT1 provides mechanical strength and resilience to keratinocytes, protecting skin against physical stress. Pathogenic variants in KRT1 disrupt the intermediate filament network, causing skin fragility and leading to disorders such as **epidermolytic hyperkeratosis**, characterized by blistering and thickened skin[1][2][3]. Beyond structural roles, KRT1 also contributes to the regulation of keratinocyte differentiation and inflammatory responses in the epidermis[5]. There are currently no drugs that directly target KRT1, and modulation could pose risks to skin integrity.

Other names
Keratin 1KRT1KRTACK-1K1KRT1A67 kDa cytokeratinCytokeratin-1Hair alpha proteinType-II keratin Kb1AEI2CK1EHKEHK1EPPKNEPPKcytokeratin 1epidermolytic hyperkeratosis 1
02

Mechanism of action

Not applicable (no known direct therapeutic targeting)

03

Biological functions

Structural framework for keratinocytesSkin barrier formationResilience to physical stressRegulation of keratinocyte differentiationModulation of inflammatory signaling pathways
04

Disease associations

Inherited skin disorders (e.g., epidermolytic hyperkeratosis, epidermolytic ichthyosis)Barrier defects in skinSkin fragility syndromesPotential roles in other inflammatory skin diseases
05

Safety considerations

Structural impairment leads to skin fragility—therapeutic intervention would risk barrier function and may result in impaired wound healing, increased susceptibility to infection, and severe dermatitis if antagonized
06

Biomarkers

Mutations in KRT1 are biomarkers for epidermolytic hyperkeratosis and related hereditary ichthyoses

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