6AT0: Heterochromatin protein 1

Chromodomain HP1 with a p-nitro-L-phenylalanine mutation at position 24 bound to histone H3 peptide containing trimethyl lysine. Determined by X-ray diffraction at 1.28 Å resolution. Released 6 Dec 2017.

Method
X-ray diffraction
Resolution
1.28 Å
Organism
Drosophila melanogaster
Chains
2
Atoms
579
Mol. weight
9.35 kDa
Released
6 Dec 2017

Explore 6AT0 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6AT0 contains 3 α-helices and 6 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: 3 helices, 5 β-strands

ElementResiduesLengthSheet
β-strand23-2531
β-strand26-35102
β-strand38-4582
α-helix50-523
β-strand54-5742
α-helix58-603
β-strand61-6221
α-helix64-7310
Chain P: 0 helices, 1 β-strand
ElementResiduesLengthSheet
β-strand6-831

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Heterochromatin protein 1Aprotein69Drosophila melanogasterP05205 (AlphaFold model)
trimethyl lysine histone H3 tail peptidePprotein6Drosophila melanogasterP02299 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>6AT0_1 Heterochromatin protein 1 (chains A)
MKKHHHHHHAEEEEEEFAVEKIIDRRVRKGMVEYYLKWKGYPETENTWEPENNLDCQDLI
QQYEASRKD
Sequence of entity 2 (P), FASTA
>6AT0_2 trimethyl lysine histone H3 tail peptide (chains P)
QTARKS

Primary citation

Investigation of Trimethyllysine Binding by the HP1 Chromodomain via Unnatural Amino Acid Mutagenesis. Baril, S.A., Koenig, A.L., Krone, M.W. et al. J Am Chem Soc (2017) 139:17253-17256. DOI 10.1021/jacs.7b09223 · PubMed

Other PDB entries of the same protein (UniProt P05205 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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