Target intelligence / Profile preview

Bone Morphogenetic Protein Receptor Type-1 (BMPR1)

Target
BMPR1
Molecular classification
Receptor, Serine/threonine kinase receptor, Transmembrane protein
01

Overview

Bone morphogenetic protein receptor type-1 (BMPR1) refers to a family of transmembrane serine/threonine kinase receptors that mediate the cellular effects of bone morphogenetic proteins (BMPs). There are four type I BMP receptors: BMPR1A, BMPR1B, ACVRL1, and ACVR1. Upon ligand binding, the type II receptor phosphorylates and activates the associated type I receptor. Activated BMPR-I then phosphorylates SMAD effectors, leading to gene expression changes. BMP/BMPRI signaling regulates diverse processes including cell fate determination, apoptosis, adipocyte development, and chondrocyte differentiation. Mutations in BMPR1 genes are linked to diseases such as juvenile polyposis syndrome and fibrodysplasia ossificans progressiva.

Other names
BMPR1ABMPR1BACVRL1ACVR1ALK-2
02

Mechanism of action

Kinase activation via phosphorylation by type II receptor, followed by SMAD phosphorylation and gene expression regulation (canonical pathway); activation of MAPK signaling cascades (non-canonical pathway)

03

Biological functions

Signal transductionCell fate determinationMesoderm specificationApoptosis regulationAdipocyte developmentChondrocyte differentiationOsteoblast extracellular matrix depositionRepression of WNT signaling
04

Disease associations

Juvenile polyposis syndromeFibrodysplasia ossificans progressivaCancer
05

Safety considerations

Aberrant regulation implicated in cancer progressionDysregulation leads to abnormal ossification (fibrodysplasia ossificans progressiva)

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