1M1A: Histone H3.3C

Ligand binding alters the structure and dynamics of nucleosomal DNA. Determined by X-ray diffraction at 2.65 Å resolution. Released 18 Feb 2003.

Method
X-ray diffraction
Resolution
2.65 Å
Organisms
Synthetic construct, Xenopus laevis
Chains
10
Atoms
12,378
Mol. weight
200.86 kDa
Ligands
IMT, ABU, BAL, DIB
Released
18 Feb 2003

Explore 1M1A in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

1M1A contains 37 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-helix441-4422
α-helix445-45612
α-helix464-47613
β-strand483-48421
α-helix486-51328
β-strand518-51922
α-helix521-53111
Chain B: 4 helices, 3 β-strands
ElementResiduesLengthSheet
α-helix26-283
α-helix31-4010
β-strand45-4622
α-helix50-7526
β-strand80-8121
α-helix83-9210
β-strand97-9823
Chain C: 5 helices, 3 β-strands
ElementResiduesLengthSheet
α-helix827-83610
β-strand842-84324
α-helix846-87227
β-strand877-87825
α-helix880-88910
α-helix891-8966
β-strand900-90236
α-helix913-9153
Chain D: 4 helices, 2 β-strands
ElementResiduesLengthSheet
α-helix1235-124511
β-strand1250-125125
α-helix1253-128028
β-strand1285-128624
α-helix1288-129811
α-helix1301-131919
Chain E: 4 helices, 2 β-strands
ElementResiduesLengthSheet
α-helix645-65511
α-helix664-67613
β-strand683-68427
α-helix686-71328
β-strand718-71928
α-helix721-73111
Chain F: 5 helices, 3 β-strands
ElementResiduesLengthSheet
α-helix219-2224
α-helix225-2284
α-helix231-24010
β-strand245-24628
α-helix250-27526
β-strand280-28127
α-helix283-29210
β-strand296-29836
Chain G: 6 helices, 3 β-strands
ElementResiduesLengthSheet
α-helix1017-10204
α-helix1027-103610
β-strand1042-104329
α-helix1046-107126
β-strand1077-1078210
α-helix1080-10889
α-helix1091-10966
β-strand1101-110223
α-helix1113-11153
Chain H: 4 helices, 2 β-strands
ElementResiduesLengthSheet
α-helix1435-144511
β-strand1450-1451210
α-helix1453-148028
β-strand1485-148629
α-helix1488-149811
α-helix1501-151919

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Palindromic 146 Base Pair DNA FragmentI, JDNA146Synthetic construct
Histone H3.3CA, Eprotein135Xenopus laevisP02302 (AlphaFold model)
Histone H4B, Fprotein102Xenopus laevisP62799 (AlphaFold model)
Histone H2A type 1C, Gprotein129Xenopus laevisP06897 (AlphaFold model)
Histone H2BD, Hprotein125Xenopus laevisP02281 (AlphaFold model)
Sequence of entity 1 (I, J), FASTA
>1M1A_1 Palindromic 146 Base Pair DNA Fragment (chains I, J)
ATCAATATCCACCTGCAGATTCTACCAAAAGTGTATTTGGAAACTGCTCCATCAAAAGGC
ATGTTCAGCGGAATTCCGCTGAACATGCCTTTTGATGGAGCAGTTTCCAAATACACTTTT
GGTAGAATCTGCAGGTGGATATTGAT
Sequence of entity 2 (A, E), FASTA
>1M1A_2 Histone H3.3C (chains A, E)
ARTKQTARKSTGGKAPRKQLVTKAAKKCAPATGGVKKPHRYRPGTVALREIRRYQKSTEL
LIRKLPFQRLVREIAQDFKTDLRFQSSAVMALQEASEAYLVALFEDTNLCAIHAKRVTIM
PKDIQLARRIRGERA
Sequence of entity 3 (B, F), FASTA
>1M1A_3 Histone H4 (chains B, F)
SGRGKGGKGLGKGGAKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETRGVLKV
FLENVIRDAVTYTEHAKRKTVTAMDVVYALKRQGRTLYGFGG
Sequence of entity 4 (C, G), FASTA
>1M1A_4 Histone H2A type 1 (chains C, G)
SGRGKQGGKTRAKAKTRSSRAGLQFPVGRVHRLLRKGNYAERVGAGAPVYLAAVLEYLTA
EILELAGNAARDNKKTRIIPRHLQLAVRNDEELNKLLGRVTIAQGGVLPNIQSVLLPKKT
ESAKSAKSK
Sequence of entity 5 (D, H), FASTA
>1M1A_5 Histone H2B (chains D, H)
PEPAKSAPAPKKGSKKAVTKTQKKDGKKRRKTRKESYAIYVYKVLKQVHPDTGISSKAMS
IMNSFVNDVFERIAGEASRLAHYNKRSTITSREIQTAVRLLLPGELAKHAVSEGTKAVTK
YTSAK

Ligands and cofactors

IDNameFormulaCopies
IMT4-amino-(1-methylimidazole)-2-carboxylic acidC5 H7 N3 O22
ABUGamma-amino-butanoic acidC4 H9 N O21
BALBeta-alanineC3 H7 N O21
DIB3-amino-(dimethylpropylamine)C5 H14 N21
PYB4-amino-(1-methylpyrrole)-2-carboxylic acidC6 H8 N2 O26
MNManganese (II) ionMn10

Primary citation

Crystal Structures of Nucleosome Core Particles in Complex with Minor Groove DNA-binding Ligands. Suto, R.K., Edayathumangalam, R.S., White, C.L. et al. J Mol Biol (2003) 326:371-380. DOI 10.1016/S0022-2836(02)01407-9 · PubMed

Other PDB entries of the same protein (UniProt P02302 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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