9NBX: PAK1

Crystal structure of PAK1 bound to C2. Determined by X-ray diffraction at 2.15 Å resolution. Released 25 Jun 2025.

Method
X-ray diffraction
Resolution
2.15 Å
Organism
Homo sapiens
Chains
2
Atoms
4,342
Mol. weight
123.54 kDa
Ligands
A1BW5
Released
25 Jun 2025

Explore 9NBX in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 19 helices, 15 β-strands

ElementResiduesLengthSheet
α-helix252-2609
β-strand26311
α-helix266-2683
β-strand270-27562
β-strand285-28952
β-strand295-29842
α-helix310-32011
β-strand32713
β-strand330-33232
β-strand33511
β-strand343-34532
β-strand35113
α-helix352-3587
α-helix363-38220
β-strand385-38624
α-helix392-3943
β-strand395-39733
β-strand403-40533
β-strand412-41324
β-strand42115
α-helix428-4303
α-helix433-4364
β-strand44115
α-helix445-45915
α-helix469-47911
α-helix482-4843
α-helix487-4893
α-helix492-50110
α-helix510-5112
α-helix512-5154
α-helix519-5235
α-helix524-5263
α-helix527-5304
α-helix531-54010
Chain B: 20 helices, 9 β-strands
ElementResiduesLengthSheet
α-helix257-2604
α-helix2621
α-helix266-2694
β-strand270-27566
β-strand283-28976
β-strand295-30286
α-helix309-32113
β-strand32717
α-helix328-3292
β-strand330-33676
β-strand339-34576
β-strand35117
α-helix352-3587
α-helix363-38220
α-helix392-3943
β-strand395-39737
β-strand403-40537
α-helix423-4242
α-helix433-4364
α-helix444-45916
α-helix469-47810
α-helix487-4893
α-helix492-50110
α-helix510-5112
α-helix512-5154
α-helix519-5235
α-helix524-5263
α-helix527-5304
α-helix531-54010

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Glutathione S-transferase class-mu 26 kDa isozyme,Serine/threonine-protein kinase PAK 1A, Bprotein537Homo sapiensP08515 (AlphaFold model), Q13153 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>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

Ligands and cofactors

IDNameFormulaCopies
A1BW5(6M)-8-(3-aminopropyl)-6-(4-butoxy-2-methylphenyl)-2-(methylamino)pyrido[2,3-d]…C22 H29 N5 O22

Water and common crystallization additives (DMS) are not listed.

Primary citation

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:

Browse structure collections

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