Structure
| PDB | Resolution (Å) | PDB name |
|---|---|---|
| 1CF4 | CDC42/ACK GTPASE-BINDING DOMAIN COMPLEX | |
| 1U46 | 2.0 | Crystal Structure of the Unphosphorylated Kinase Domain of the Tyrosine Kinase ACK1 |
| 1U4D | 2.1 | Structure of the ACK1 Kinase Domain bound to Debromohymenialdisine |
| 1U54 | 2.8 | Crystal Structures of the Phosphorylated and Unphosphorylated Kinase Domains of the CDC42-associated Tyrosine Kinase ACK1 bound to AMP-PCP |
| 3EQP | 2.3 | Crystal Structure of Ack1 with compound T95 |
| 3EQR | 2.0 | Crystal Structure of Ack1 with compound T74 |
| 4EWH | 2.5 | Co-crystal structure of ACK1 with inhibitor |
| 4HZR | 1.31 | Crystal structure of Ack1 kinase domain |
| 4HZS | 3.23 | Crystal structure of Ack1 kinase domain with C-terminal SH3 domain |
| 4ID7 | 3.0 | ACK1 kinase in complex with the inhibitor cis-3-[8-amino-1-(4-phenoxyphenyl)imidazo[1,5-a]pyrazin-3-yl]cyclobutanol |
| 5ZXB | 2.198 | Crystal structure of ACK1 with compound 10d |
| 6VQM | 2.87 | Crystal Structure Analysis of human ACK1 |
| 7KP6 | 1.79 | Structure of Ack1 kinase in complex with a selective inhibitor |
| 8FE9 | 3.2 | Crystal structure of Ack1 kinase K161Q mutant in complex with the selective inhibitor (R)-9b |
| 8FZ3 | 2.784 | Sterile Alpha Motif of Human Translocation ETS Leukemia, Non-Polymer Crystal Form |
