4V2W: JMJD2A

JMJD2A complexed with ni(ii), nog and histone H3K27me3 peptide (16-35). Determined by X-ray diffraction at 1.81 Å resolution. Released 26 Nov 2014.

Method
X-ray diffraction
Resolution
1.81 Å
Organism
HOMO SAPIENS
Chains
3
Atoms
6,476
Mol. weight
91.41 kDa
Ligands
NI, ZN, OGA
Released
26 Nov 2014

Explore 4V2W in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4V2W contains 42 α-helices and 36 β-strands across 3 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: 20 helices, 18 β-strands

ElementResiduesLengthSheet
α-helix13-142
β-strand15-1731
α-helix21-244
α-helix27-3610
α-helix39-424
β-strand44-4741
β-strand66-6722
β-strand71-7883
β-strand81-8883
β-strand92-9322
α-helix94-1018
α-helix108-1103
α-helix114-12411
β-strand131-13223
β-strand133-13751
α-helix156-1605
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
β-strand267-27041
β-strand275-28065
β-strand284-29181
α-helix296-3027
α-helix318-3247
α-helix326-3338
α-helix346-3472
α-helix348-3536
Chain B: 22 helices, 17 β-strands
ElementResiduesLengthSheet
β-strand15-1736
α-helix21-244
α-helix27-3610
α-helix39-424
β-strand44-4746
α-helix62-643
β-strand66-6727
β-strand71-7888
β-strand81-8888
β-strand92-9327
α-helix94-1029
α-helix108-1103
α-helix114-12411
α-helix129-1302
β-strand131-13228
β-strand133-13756
α-helix158-1647
β-strand175-17956
β-strand184-18859
α-helix189-1902
α-helix191-1933
β-strand195-20396
β-strand206-21169
α-helix213-2153
α-helix216-22611
α-helix228-2336
α-helix237-2404
β-strand243-24538
α-helix247-2526
β-strand258-26259
β-strand267-27046
β-strand275-28069
β-strand284-29186
α-helix296-3027
α-helix318-3247
α-helix326-3283
α-helix329-3335
α-helix345-3473
α-helix348-3525
Chain C: 0 helices, 1 β-strand
ElementResiduesLengthSheet
β-strand2614

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Lysine-specific demethylase 4AA, Bprotein381HOMO SAPIENSO75164 (AlphaFold model)
Histone H3.1TCprotein20HOMO SAPIENSQ16695 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>4V2W_1 LYSINE-SPECIFIC DEMETHYLASE 4A (chains A, B)
MHHHHHHSSGVDLGTENLYFQSMASESETLNPSARIMTFYPTMEEFRNFSRYIAYIESQG
AHRAGLAKVVPPKEWKPRASYDDIDDLVIPAPIQQLVTGQSGLFTQYNIQKKAMTVREFR
KIANSDKYCTPRYSEFEELERKYWKNLTFNPPIYGADVNGTLYEKHVDEWNIGRLRTILD
LVEKESGITIEGVNTPYLYFGMWKTSFAWHTEDMDLYSINYLHFGEPKSWYSVPPEHGKR
LERLAKGFFPGSAQSCEAFLRHKMTLISPLMLKKYGIPFDKVTQEAGEFMITFPYGYHAG
FNHGFNCAESTNFATRRWIEYGKQAVLCSCRKDMVKISMDVFVRKFQPERYKLWKAGKDN
TVIDHTLPTPEAAEFLKESEL
Sequence of entity 2 (C), FASTA
>4V2W_2 HISTONE H3.1T (chains C)
PRKQLATKAARKSAPATGGV

Ligands and cofactors

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

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

Primary citation

Studies on the Catalytic Domains of Multiple Jmjc Oxygenases Using Peptide Substrates. Williams, S.T., Walport, L.J., Hopkinson, R.J. et al. Epigenetics (2014) 9:1596. DOI 10.4161/15592294.2014.983381 · PubMed

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

Browse structure collections

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