Structure of Ack1 kinase in complex with a selective inhibitor. Determined by X-ray diffraction at 1.79 Å resolution. Released 9 Feb 2022.
Explore 7KP6 in 3D Show helices and sheets RCSB PDB PDBe
7KP6 contains 41 α-helices and 28 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 119-120 | 2 | 1 |
| α-helix | 123-125 | 3 | |
| β-strand | 126-134 | 9 | 1 |
| β-strand | 139-146 | 8 | 1 |
| β-strand | 152-159 | 8 | 1 |
| α-helix | 169-181 | 13 | |
| β-strand | 189 | 1 | 2 |
| α-helix | 190-191 | 2 | |
| β-strand | 192-196 | 5 | 1 |
| α-helix | 201 | 1 | |
| β-strand | 202-206 | 5 | 1 |
| β-strand | 212 | 1 | 2 |
| α-helix | 213-217 | 5 | |
| α-helix | 221-223 | 3 | |
| α-helix | 226-245 | 20 | |
| β-strand | 248-249 | 2 | 3 |
| α-helix | 255-257 | 3 | |
| β-strand | 258-262 | 5 | 2 |
| β-strand | 265-268 | 4 | 2 |
| β-strand | 275-276 | 2 | 3 |
| α-helix | 277-278 | 2 | |
| β-strand | 284-285 | 2 | 4 |
| α-helix | 286-287 | 2 | |
| α-helix | 294-296 | 3 | |
| α-helix | 299-304 | 6 | |
| β-strand | 306-307 | 2 | 4 |
| α-helix | 309-324 | 16 | |
| α-helix | 328-329 | 2 | |
| α-helix | 336-340 | 5 | |
| α-helix | 341-345 | 5 | |
| α-helix | 350-353 | 4 | |
| α-helix | 358-367 | 10 | |
| α-helix | 372-374 | 3 | |
| α-helix | 376-377 | 2 | |
| α-helix | 378-387 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 119-120 | 2 | 1 |
| α-helix | 123-125 | 3 | |
| β-strand | 126-134 | 9 | 1 |
| β-strand | 139-146 | 8 | 1 |
| β-strand | 152-159 | 8 | 1 |
| α-helix | 168-181 | 14 | |
| β-strand | 189 | 1 | 5 |
| α-helix | 190-191 | 2 | |
| β-strand | 192-196 | 5 | 1 |
| α-helix | 201 | 1 | |
| β-strand | 202-206 | 5 | 1 |
| β-strand | 211-212 | 2 | 5 |
| α-helix | 213-220 | 8 | |
| α-helix | 221-223 | 3 | |
| α-helix | 226-245 | 20 | |
| β-strand | 248-249 | 2 | 6 |
| α-helix | 255-257 | 3 | |
| β-strand | 258-262 | 5 | 5 |
| β-strand | 265-268 | 4 | 5 |
| β-strand | 275-276 | 2 | 6 |
| α-helix | 277-278 | 2 | |
| β-strand | 284-285 | 2 | 7 |
| α-helix | 294-296 | 3 | |
| α-helix | 299-304 | 6 | |
| β-strand | 306-307 | 2 | 7 |
| α-helix | 309-324 | 16 | |
| α-helix | 328-329 | 2 | |
| α-helix | 336-340 | 5 | |
| α-helix | 341-345 | 5 | |
| α-helix | 350-353 | 4 | |
| α-helix | 358-367 | 10 | |
| α-helix | 372-374 | 3 | |
| α-helix | 376-377 | 2 | |
| α-helix | 378-386 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Activated CDC42 kinase 1 | A, B | protein | 287 | Homo sapiens | Q07912 (AlphaFold model) |
>7KP6_1 Activated CDC42 kinase 1 (chains A, B) GAMGSGEGPLQSLTCLIGEKDLRLLEKLGDGSFGVVRRGEWDAPSGKTVSVAVKCLKPDV LSQPEAMDDFIREVNAMHSLDHRNLIRLYGVVLTPPMKMVTELAPLGSLLDRLRKHQGHF LLGTLSRYAVQVAEGMGYLESKRFIHRDLAARNLLLATRDLVKIGDFGLMRALPQNDDHY VMQEHRKVPFAWCAPESLKTRTFSHASDTWMFGVTLWEMFTYGQEPWIGLNGSQILHKID KEGERLPRPEDCPQDIYNVMVQCWAHKPEDRPTFVALRDFLLEAQPT
| ID | Name | Formula | Copies |
|---|---|---|---|
| WTP | 5-chloro-N~2~-[4-(4-methylpiperazin-1-yl)phenyl]-N~4~-{[(2R)-oxolan-2-yl]methyl… | C20 H27 Cl N6 O | 2 |
Water and common crystallization additives (CL) are not listed.
Inhibiting ACK1-mediated phosphorylation of C-terminal Src kinase counteracts prostate cancer immune checkpoint blockade resistance. Sridaran, D., Chouhan, S., Mahajan, K. et al. Nat Commun (2022) 13:6929-6929. DOI 10.1038/s41467-022-34724-5 · PubMed
Other PDB entries of the same protein (UniProt Q07912 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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