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- 2ZMD: crystal structure of human mps1 catalytic domain t686a mutant in complex with sp600125 inhibitor (10.1074/JBC.M803026200 )
- 4FEU: crystal structure of the aminoglycoside phosphotransferase aph(3')-ia, with substrate kanamycin and small molecule inhibitor anthrapyrazolone sp600125 (10.1042/BJ20130317 )
- 5LVL: human pdk1 kinase domain in complex with compound ps653 bound to the atp-binding site (10.1016/J.CHEMBIOL.2016.06.017 )
- 1UKI: structural basis for the selective inhibition of jnk1 by the scaffolding protein jip1 and sp600125 (10.1038/SJ.EMBOJ.7600212 )
- 1PMV: the structure of jnk3 in complex with a dihydroanthrapyrazole inhibitor (10.1016/S1074-5521(03)00159-5 )