Crystal structure of PAK1 bound to C2. Determined by X-ray diffraction at 2.15 Å resolution. Released 25 Jun 2025.
Explore 9NBX in 3D Show helices and sheets RCSB PDB PDBe
9NBX contains 39 α-helices and 24 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 |
|---|---|---|---|
| α-helix | 252-260 | 9 | |
| β-strand | 263 | 1 | 1 |
| α-helix | 266-268 | 3 | |
| β-strand | 270-275 | 6 | 2 |
| β-strand | 285-289 | 5 | 2 |
| β-strand | 295-298 | 4 | 2 |
| α-helix | 310-320 | 11 | |
| β-strand | 327 | 1 | 3 |
| β-strand | 330-332 | 3 | 2 |
| β-strand | 335 | 1 | 1 |
| β-strand | 343-345 | 3 | 2 |
| β-strand | 351 | 1 | 3 |
| α-helix | 352-358 | 7 | |
| α-helix | 363-382 | 20 | |
| β-strand | 385-386 | 2 | 4 |
| α-helix | 392-394 | 3 | |
| β-strand | 395-397 | 3 | 3 |
| β-strand | 403-405 | 3 | 3 |
| β-strand | 412-413 | 2 | 4 |
| β-strand | 421 | 1 | 5 |
| α-helix | 428-430 | 3 | |
| α-helix | 433-436 | 4 | |
| β-strand | 441 | 1 | 5 |
| α-helix | 445-459 | 15 | |
| α-helix | 469-479 | 11 | |
| α-helix | 482-484 | 3 | |
| α-helix | 487-489 | 3 | |
| α-helix | 492-501 | 10 | |
| α-helix | 510-511 | 2 | |
| α-helix | 512-515 | 4 | |
| α-helix | 519-523 | 5 | |
| α-helix | 524-526 | 3 | |
| α-helix | 527-530 | 4 | |
| α-helix | 531-540 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 257-260 | 4 | |
| α-helix | 262 | 1 | |
| α-helix | 266-269 | 4 | |
| β-strand | 270-275 | 6 | 6 |
| β-strand | 283-289 | 7 | 6 |
| β-strand | 295-302 | 8 | 6 |
| α-helix | 309-321 | 13 | |
| β-strand | 327 | 1 | 7 |
| α-helix | 328-329 | 2 | |
| β-strand | 330-336 | 7 | 6 |
| β-strand | 339-345 | 7 | 6 |
| β-strand | 351 | 1 | 7 |
| α-helix | 352-358 | 7 | |
| α-helix | 363-382 | 20 | |
| α-helix | 392-394 | 3 | |
| β-strand | 395-397 | 3 | 7 |
| β-strand | 403-405 | 3 | 7 |
| α-helix | 423-424 | 2 | |
| α-helix | 433-436 | 4 | |
| α-helix | 444-459 | 16 | |
| α-helix | 469-478 | 10 | |
| α-helix | 487-489 | 3 | |
| α-helix | 492-501 | 10 | |
| α-helix | 510-511 | 2 | |
| α-helix | 512-515 | 4 | |
| α-helix | 519-523 | 5 | |
| α-helix | 524-526 | 3 | |
| α-helix | 527-530 | 4 | |
| α-helix | 531-540 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Glutathione S-transferase class-mu 26 kDa isozyme,Serine/threonine-protein kinase PAK 1 | A, B | protein | 537 | Homo sapiens | P08515 (AlphaFold model), Q13153 (AlphaFold model) |
>9NBX_1 Glutathione S-transferase class-mu 26 kDa isozyme,Serine/threonine-protein kinase PAK 1 (chains A, B) MHHHHHHHHGSPILGYWKIKGLVQPTRLLLEYLEEKYEEHLYERDEGDKWRNKKFELGLE FPNLPYYIDGDVKLTQSMAIIRYIADKHNMLGGCPKERAEISMLEGAVLDIRYGVSRIAY SKDFETLKVDFLSKLPEMLKMFKDRLCHKTYLNGDHVTHPDFMLYDALDVVLYMDPMCLD AFPKLVCFKKRIEAIPQIDKYLKSSKYIAWPLQGWQATFGGGDHPPKSDGENLYFQGSDE EILEKLRSIVSVGDPKKKYTRFEKIGQGASGTVYTAMDVATGQEVAIKQMNLQQQPKKEL IINEILVMRENKNPNIVNYLDSYLVGDELWVVMEYLAGGSLTDVVTETCMDEGQIAAVCR ECLQALEFLHSNQVIHRNIKSDNILLGMDGSVKLTDFGFCAQITPEQSKRSEMVGTPYWM APEVVTRKAYGPKVDIWSLGIMAIEMIEGEPPYLNENPLRALYLIATNGTPELQNPEKLS AIFRDFLNRCLEMDVEKRGSAKELLQHQFLKIAKPLSSLTPLIAAAKEATKNNHGNS
| ID | Name | Formula | Copies |
|---|---|---|---|
| A1BW5 | (6M)-8-(3-aminopropyl)-6-(4-butoxy-2-methylphenyl)-2-(methylamino)pyrido[2,3-d]… | C22 H29 N5 O2 | 2 |
Water and common crystallization additives (DMS) are not listed.
Integrating Hydrogen Exchange with Molecular Dynamics for Improved Ligand Binding Predictions. Walters, B.T., Patapoff, A.W., Kiefer, J.R. et al. J Chem Inf Model (2025) 65:6144-6154. DOI 10.1021/acs.jcim.5c00397 · PubMed
Other PDB entries of the same protein (UniProt P08515 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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