9RXU: Histone H3.2

RAPTA-C (Ruthenium[II]-cymene-phosphaadamantane) cancer drug binding to the nucleosome core. Determined by X-ray diffraction at 2.3 Å resolution. Released 22 Jul 2026.

Method
X-ray diffraction
Resolution
2.3 Å
Organisms
Xenopus laevis, Homo sapiens
Chains
10
Atoms
12,126
Mol. weight
199.62 kDa
Ligands
A1JKP, MG
Released
22 Jul 2026

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

Secondary structure: helices and β-sheets

9RXU contains 40 α-helices and 20 β-strands across 8 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: 5 helices, 2 β-strands

ElementResiduesLengthSheet
α-helix41-422
α-helix45-5612
α-helix64-7613
β-strand83-8421
α-helix86-11328
β-strand118-11922
α-helix121-13010
Chain B: 4 helices, 3 β-strands
ElementResiduesLengthSheet
α-helix25-284
α-helix31-4010
β-strand45-4622
α-helix50-7526
β-strand80-8121
α-helix83-9210
β-strand96-9833
Chain C: 6 helices, 3 β-strands
ElementResiduesLengthSheet
α-helix17-215
α-helix27-3610
β-strand42-4324
α-helix47-7226
β-strand77-7825
α-helix80-8910
α-helix91-966
β-strand100-10236
α-helix113-1153
Chains D and H: 4 helices, 2 β-strands
ElementResiduesLengthSheet
α-helix35-4511
β-strand50-5125
α-helix53-8028
β-strand85-8624
α-helix88-9811
α-helix101-12020
Chain E: 5 helices, 2 β-strands
ElementResiduesLengthSheet
α-helix41-422
α-helix45-5612
α-helix64-7815
β-strand83-8427
α-helix86-11328
β-strand118-11928
α-helix121-13010
Chain F: 5 helices, 3 β-strands
ElementResiduesLengthSheet
α-helix20-223
α-helix25-284
α-helix31-4010
β-strand45-4628
α-helix50-7526
β-strand80-8127
α-helix83-9210
β-strand96-9836
Chain G: 7 helices, 3 β-strands
ElementResiduesLengthSheet
α-helix17-215
α-helix27-359
β-strand42-4329
α-helix47-7226
β-strand77-78210
α-helix80-889
α-helix91-966
β-strand100-10233
α-helix113-1153
α-helix117-1182

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone H3.2A, Eprotein135Xenopus laevisP84233 (AlphaFold model)
Histone H4B, Fprotein102Xenopus laevisP62799 (AlphaFold model)
Histone H2AC, Gprotein128Xenopus laevisQ6AZJ8 (AlphaFold model)
Histone H2B 1.1D, Hprotein125Xenopus laevisP02281 (AlphaFold model)
DNA (145-mer)IDNA145Homo sapiens
DNA (145-mer)JDNA145Homo sapiens
Sequence of entity 1 (A, E), FASTA
>9RXU_1 Histone H3.2 (chains A, E)
ARTKQTARKSTGGKAPRKQLATKAARKSAPATGGVKKPHRYRPGTVALREIRRYQKSTEL
LIRKLPFQRLVREIAQDFKTDLRFQSSAVMALQEASEAYLVALFEDTNLCAIHAKRVTIM
PKDIQLARRIRGERA
Sequence of entity 2 (B, F), FASTA
>9RXU_2 Histone H4 (chains B, F)
SGRGKGGKGLGKGGAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLKV
FLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
Sequence of entity 3 (C, G), FASTA
>9RXU_3 Histone H2A (chains C, G)
SGRGKQGGKTRAKAKTRSSRAGLQFPVGRVHRLLRKGNYAERVGAGAPVYLAAVLEYLTA
EILELAGNAARDNKKTRIIPRHLQLAVRNDEELNKLLGRVTIAQGGVLPNIQSVLLPKKT
ESSKSKSK
Sequence of entity 4 (D, H), FASTA
>9RXU_4 Histone H2B 1.1 (chains D, H)
PEPAKSAPAPKKGSKKAVTKTQKKDGKKRRKTRKESYAIYVYKVLKQVHPDTGISSKAMS
IMNSFVNDVFERIAGEASRLAHYNKRSTITSREIQTAVRLLLPGELAKHAVSEGTKAVTK
YTSAK
Sequence of entity 5 (I), FASTA
>9RXU_5 DNA (145-MER) (chains I)
ATCAATATCCACCTGCAGATACTACCAAAAGTGTATTTGGAAACTGCTCCATCAAAAGGC
ATGTTCAGCTGAATCAGCTGAACATGCCTTTTGATGGAGCAGTTTCCAAATACACTTTTG
GTAGTATCTGCAGGTGGATATTGAT
Sequence of entity 6 (J), FASTA
>9RXU_6 DNA (145-MER) (chains J)
ATCAATATCCACCTGCAGATACTACCAAAAGTGTATTTGGAAACTGCTCCATCAAAAGGC
ATGTTCAGCTGATTCAGCTGAACATGCCTTTTGATGGAGCAGTTTCCAAATACACTTTTG
GTAGTATCTGCAGGTGGATATTGAT

Ligands and cofactors

IDNameFormulaCopies
A1JKPRuthenium[II]-cymene-phosphaadamantaneC16 H26 N3 P Ru3
MGMagnesium ionMg1

Water and common crystallization additives (SO4) are not listed.

Primary citation

RAPTA-C (Ruthenium[II]-cymene-phosphaadamantane) cancer drug binding to the nucleosome core. Davey, C.A. To be published.

Other PDB entries of the same protein (UniProt P84233 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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