4LLB: MOZ double PHD finger histone H3K14ac complex

Crystal Structure of MOZ double PHD finger histone H3K14ac complex. Determined by X-ray diffraction at 2.5 Å resolution. Released 16 Oct 2013.

Method
X-ray diffraction
Resolution
2.5 Å
Organism
Homo sapiens
Chains
4
Atoms
2,281
Mol. weight
36.13 kDa
Ligands
ZN
Released
16 Oct 2013

Explore 4LLB in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4LLB contains 12 α-helices and 14 β-strands across 4 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.

Chains A and B: 5 helices, 6 β-strands

ElementResiduesLengthSheet
α-helix195-1973
α-helix203-2064
β-strand20911
β-strand228-22921
β-strand236-23721
α-helix246-2538
β-strand26512
α-helix275-2773
β-strand279-28022
β-strand287-28822
α-helix290-2923
Chains C and D: 1 helix, 1 β-strand
ElementResiduesLengthSheet
β-strand312
α-helix4-118

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone acetyltransferase KAT6AA, Bprotein136Homo sapiensQ92794 (AlphaFold model)
Histone H3.1C, Dprotein21Homo sapiensP68431 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>4LLB_1 Histone acetyltransferase KAT6A (chains A, B)
GSHMLELPHEKDKPVAEPIPICSFCLGTKEQNREKKPEELISCADCGNSGHPSCLKFSPE
LTVRVKALRWQCIECKTCSSCRDQGKNADNMLFCDSCDRGFHMECCDPPLTRMPKGMWIC
QICRPRKKGRKLLQKK
Sequence of entity 2 (C, D), FASTA
>4LLB_2 Histone H3.1 (chains C, D)
ARTKQTARKSTGGKAPRKQLA

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn8

Primary citation

The double PHD finger domain of MOZ/MYST3 induces alpha-helical structure of the histone H3 tail to facilitate acetylation and methylation sampling and modification. Dreveny, I., Deeves, S.E., Fulton, J. et al. Nucleic Acids Res (2014) 42:822-835. DOI 10.1093/nar/gkt931 · PubMed

Other PDB entries of the same protein (UniProt Q92794 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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