Target intelligence / Profile preview

Protein kinase domain containing, cytoplasmic (PKDCC)

Target
PKDCC
Molecular classification
Enzyme, Protein kinase, Tyrosine protein kinase, Secreted kinase (non-membrane spanning protein tyrosine kinase)
01

Overview

Protein kinase domain containing, cytoplasmic (PKDCC), also known as vertebrate lonesome kinase (VLK) and Sugen kinase 493 (SGK493), is a secreted protein tyrosine kinase that phosphorylates extracellular and secretory pathway proteins. It plays a critical role in skeletal system development, including bone elongation through regulation of chondrocyte differentiation, and is also implicated in extracellular matrix and platelet signaling. PKDCC influences the Hedgehog signaling pathway and is linked via genetic studies to congenital disorders affecting bones, limbs, and craniofacial features. Its broad expression across multiple tissues highlights its fundamental role in developmental biology, but no drug directly targeting PKDCC is currently approved[1][2][3][5].

Other names
Vertebrate lonesome kinase (VLK)Sugen kinase 493 (SGK493)SgK493Vlkextracellular tyrosine-protein kinase PKDCCprotein kinase-like protein SgK493sugen kinase 493vertebrate lonesome kinase
02

Mechanism of action

Drugs (if developed) would likely function as enzymatic inhibitors (protein kinase inhibitors), modulating extracellular phosphorylation activity. Indirect mechanisms may involve regulation of signaling cascades like Hedgehog pathway or extracellular matrix-related signaling[3].

03

Biological functions

Peptidyl-tyrosine phosphorylation (of extracellular proteins and endogenous secretory proteins)Skeletal system development (bone growth, chondrocyte differentiation)Regulation of extracellular signalingNegative regulation of Hedgehog signaling (by promoting Smoothened degradation)Platelet activation and degranulation (phosphorylates extracellular matrix proteins influencing platelet functions)Protein transport from Golgi to plasma membrane (indirectly)
04

Disease associations

Congenital bone and limb defects (e.g. rhizomelic limb shortening with dysmorphic features, short stature and advanced bone age, early-onset osteoarthritis)Craniofacial morphological variations and orofacial cleftingPotential role in bone mineral density regulationOther (under investigation, e.g. tissue morphogenesis)
05

Safety considerations

Given its essential role in skeletal development and extracellular protein phosphorylation, inhibition could cause adverse effects in bone growth, tissue morphogenesis, and platelet functions[3].Potential for off-target effects due to role in diverse tissues (bone, muscle, craniofacial regions, platelets)[1][3].
06

Interacting drugs

No direct, approved drugs targeting PKDCC reported in available sources; however, expression may be influenced indirectly by various experimental drug perturbations (as indicated in gene expression signatures)[3].
07

Biomarkers

PKDCC gene variants (e.g., biallelic PKDCC mutations for limb development disorders; regulatory SNPs for craniofacial variation)Expression level in tissue samples for developmental or skeletal disease risk

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