k Activin A receptor type I protein, molecular model Molecular model of the cytoplasmic domain of the activin A receptor type I ACVR1 protein beige, pale yellow and red bound to its natural inhibitor FK506binding protein 12 FKB12, orange ribbon and the synthetic inhibitor RK71807 spheres. ACVR1 plays a role in the bone morphogenic protein BMP pathway. A mutant form of the protein is responsible for the rare genetic disease fibrodysplasia ossificans progressiva FOP. FOP is a disease where fibrous tissues, including muscle, tendons and ligaments, are gradually replaced by bone ossified. The mutation in ACVR1 decreases its affinity for FKB12, leading to increased activity of the protein and therefore increased production of bone., Photo by RAMON ANDRADE 3DCIENCIASCIENCE PHOTO LIBRARY Stock Photo - Afloimages
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Activin A receptor type I protein, molecular model Molecular model of the cytoplasmic domain of the activin A receptor type I  ACVR1  protein  beige, pale yellow and red  bound to its natural inhibitor FK506 binding protein 12  FKB12, orange ribbon  and the synthetic inhibitor RK 71807  spheres . ACVR1 plays a role in the bone morphogenic protein  BMP  pathway. A mutant form of the protein is responsible for the rare genetic disease fibrodysplasia ossificans progressiva  FOP . FOP is a disease where fibrous tissues, including muscle, tendons and ligaments, are gradually replaced by bone  ossified . The mutation in ACVR1 decreases its affinity for FKB12, leading to increased activity of the protein and therefore increased production of bone., Photo by RAMON ANDRADE 3DCIENCIA SCIENCE PHOTO LIBRARY
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Activin A receptor type I protein, molecular model

Molecular model of the cytoplasmic domain of the activin A receptor type I (ACVR1) protein (beige, pale yellow and red) bound to its natural inhibitor FK506-binding protein 12 (FKB12, orange ribbon) and the synthetic inhibitor RK-71807 (spheres). ACVR1 plays a role in the bone morphogenic protein (BMP) pathway. A mutant form of the protein is responsible for the rare genetic disease fibrodysplasia ossificans progressiva (FOP). FOP is a disease where fibrous tissues, including muscle, tendons and ligaments, are gradually replaced by bone (ossified). The mutation in ACVR1 decreases its affinity for FKB12, leading to increased activity of the protein and therefore increased production of bone., Photo by RAMON ANDRADE 3DCIENCIA/SCIENCE PHOTO LIBRARY

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