FH0 · ~{N}-[4-(4-methylpiperazin-1-yl)phenyl]-4-(2-pyridin-3-yl-6,7-dihydro-4~{H}-pyrazolo[5,1-c][1,4]oxazin-3-yl) pyrimidin-2-amine

Binding sites

FH0 in 2 structures; the first of them:

• 7C3G · Crystal structure of human ALK2 kinase domain with R206H mutation in complex with a… · FH0 A501 · binds VAL214, TYR219, VAL222, ALA233, LYS235, LEU263, LEU281, THR283 and 11 more
• 7C3G · Crystal structure of human ALK2 kinase domain with R206H mutation in complex with a… · FH0 A501 · binds VAL214, TYR219, VAL222, ALA233, LYS235, LEU263, LEU281, THR283 and 10 more

Residues it binds most

LEU 4, HIS 4, LYS 4, VAL 4, TYR 4, ALA 4, ASP 4, GLU 4, GLY 4, MET 4 (residue and the binding sites it lines).

Found with

• SO4 · Sulfate ion
• EDO · 1,2-ethanediol