https://www.ncbi.nlm.nih.gov/Structure/pdb/5S7O
5S7O: XChem group deposition -- Crystal Structure of human ACVR1 in complex with FM007391c
Activin receptor type-11,2-ETHANEDIOL4-methyl-3-[4-(1-methylpiperidin-4-yl)phenyl]-5-(3,4,5-trimethoxyphenyl)pyridineL(+)-TARTARIC ACIDSULFATE ION
https://pubmed.ncbi.nlm.nih.gov/16642017/
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia...
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder of skeletal malformations and progressive extraskeletal ossification. We...