6H8P: JMJD2A/ KDM4A

JMJD2A/ KDM4A COMPLEXED WITH NI(II), NOG AND Histone H1.4(18-32)K26me3 peptide (15-mer). Determined by X-ray diffraction at 1.98 Å resolution. Released 15 Aug 2018.

Method
X-ray diffraction
Resolution
1.98 Å
Organism
Homo sapiens
Chains
4
Atoms
6,238
Mol. weight
92.81 kDa
Ligands
OGA, ZN, NI
Released
15 Aug 2018

Explore 6H8P in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6H8P contains 53 α-helices and 38 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.

Chain A: 26 helices, 18 β-strands

ElementResiduesLengthSheet
α-helix10-123
α-helix141
β-strand15-1731
α-helix21-255
α-helix27-3610
α-helix39-424
β-strand44-4741
α-helix48-503
β-strand66-6722
β-strand71-7883
β-strand81-8883
β-strand92-9322
α-helix94-1029
α-helix108-1103
α-helix114-12411
β-strand131-13223
β-strand133-13751
α-helix156-1583
α-helix159-1624
β-strand16914
β-strand175-17951
β-strand184-18855
α-helix189-1902
α-helix191-1933
β-strand195-20391
β-strand206-21165
α-helix213-2153
α-helix216-22611
α-helix228-2336
α-helix237-2404
β-strand243-24533
α-helix247-2526
β-strand258-26255
α-helix2631
β-strand267-27041
β-strand275-28065
β-strand284-29181
α-helix296-3027
α-helix303-3064
α-helix318-3247
α-helix326-3338
α-helix339-3413
α-helix346-3472
α-helix348-3536
Chain B: 27 helices, 18 β-strands
ElementResiduesLengthSheet
α-helix4-74
α-helix13-142
β-strand15-1736
α-helix21-244
α-helix27-3610
α-helix39-424
β-strand44-4746
α-helix48-503
α-helix62-643
β-strand66-6727
β-strand71-7888
β-strand81-8888
α-helix89-913
β-strand92-9327
α-helix94-1029
α-helix108-1103
α-helix114-12411
β-strand131-13228
β-strand133-13756
α-helix156-1583
α-helix159-1646
β-strand16919
β-strand175-17956
β-strand184-188510
α-helix189-1902
α-helix191-1933
β-strand195-20396
β-strand206-211610
α-helix213-2153
α-helix216-22611
α-helix228-2336
α-helix237-2404
β-strand243-24538
α-helix247-2526
β-strand258-262510
β-strand267-27046
β-strand275-280610
β-strand284-29186
α-helix296-3027
α-helix303-3064
α-helix318-3247
α-helix326-3338
α-helix345-3473
α-helix348-3503
α-helix351-3544
Chains C and D: 0 helices, 1 β-strand
ElementResiduesLengthSheet
β-strand2514

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Lysine-specific demethylase 4AA, Bprotein381Homo sapiensO75164 (AlphaFold model)
Histone H1.4C, Dprotein15Homo sapiensP10412 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>6H8P_1 Lysine-specific demethylase 4A (chains A, B)
MHHHHHHSSGVDLGTENLYFQSMASESETLNPSARIMTFYPTMEEFRNFSRYIAYIESQG
AHRAGLAKVVPPKEWKPRASYDDIDDLVIPAPIQQLVTGQSGLFTQYNIQKKAMTVREFR
KIANSDKYCTPRYSEFEELERKYWKNLTFNPPIYGADVNGTLYEKHVDEWNIGRLRTILD
LVEKESGITIEGVNTPYLYFGMWKTSFAWHTEDMDLYSINYLHFGEPKSWYSVPPEHGKR
LERLAKGFFPGSAQSCEAFLRHKMTLISPLMLKKYGIPFDKVTQEAGEFMITFPYGYHAG
FNHGFNCAESTNFATRRWIEYGKQAVLCSCRKDMVKISMDVFVRKFQPERYKLWKAGKDN
TVIDHTLPTPEAAEFLKESEL
Sequence of entity 2 (C, D), FASTA
>6H8P_2 Histone H1.4 (chains C, D)
TPVKKKARKSAGAAK

Ligands and cofactors

IDNameFormulaCopies
OGAN-oxalylglycineC4 H5 N O52
ZNZinc ionZn2
NINickel (II) ionNi2

Water and common crystallization additives (GOL, CL) are not listed.

Primary citation

Mechanistic and structural studies of KDM-catalysed demethylation of histone 1 isotype 4 at lysine 26. Walport, L.J., Hopkinson, R.J., Chowdhury, R. et al. FEBS Lett (2018) 592:3264-3273. DOI 10.1002/1873-3468.13231 · PubMed

Other PDB entries of the same protein (UniProt O75164 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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