Structure of the bone morphogenetic protein receptor ALK2 and implications for fibrodysplasia ossificans progressiva

Background: Mutations in the ALK2 kinase cause extraskeletal bone formation. Results: We solved the structure of ALK2 in complex with the inhibitor FKBP12. Conclusion: Disease mutations break critical interactions that stabilize the inactive ALK2-FKBP12 complex leading to kinase activation. Signific...

Full description

Bibliographic Details
Main Authors: Chaikuad, A, Alfano, I, Kerr, G, Sanvitale, C, Boergermann, J, Triffitt, J, Von Delft, F, Knapp, S, Knaus, P, Bullock, A
Format: Journal article
Published: 2012