2YBP: JMJD2A

JMJD2A complexed with R-2-hydroxyglutarate and histone H3K36me3 peptide (30-41). Determined by X-ray diffraction at 2.02 Å resolution. Released 30 Mar 2011.

Method
X-ray diffraction
Resolution
2.02 Å
Organism
HOMO SAPIENS
Chains
4
Atoms
6,556
Mol. weight
92 kDa
Ligands
2HG, ZN, NI
Released
30 Mar 2011

Explore 2YBP in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2YBP contains 47 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: 21 helices, 18 β-strands

ElementResiduesLengthSheet
α-helix13-142
β-strand15-1731
α-helix21-244
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-helix159-1646
β-strand175-17951
β-strand184-18854
α-helix191-1933
β-strand195-20391
β-strand206-21164
α-helix213-2153
α-helix216-22611
α-helix228-2336
α-helix237-2404
β-strand243-24533
α-helix247-2526
β-strand258-26254
β-strand267-27041
β-strand275-28064
β-strand284-29181
α-helix296-3027
β-strand31415
α-helix318-3247
α-helix329-3335
α-helix346-3472
α-helix348-3536
Chain B: 24 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
β-strand66-6727
β-strand71-7888
β-strand81-8888
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-strand175-17956
β-strand184-18859
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
α-helix2631
β-strand267-27046
β-strand275-28069
β-strand284-29186
α-helix296-3027
β-strand314110
α-helix318-3247
α-helix326-3283
α-helix329-3335
α-helix345-3473
α-helix348-3536
Chains C and D: 1 helix, 1 β-strand
ElementResiduesLengthSheet
β-strand3315
α-helix38-403

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Lysine-specific demethylase 4AA, Bprotein381HOMO SAPIENSO75164 (AlphaFold model)
Histone H3.1TC, Dprotein12HOMO SAPIENSQ16695 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>2YBP_1 LYSINE-SPECIFIC DEMETHYLASE 4A (chains A, B)
MHHHHHHSSGVDLGTENLYFQSMASESETLNPSARIMTFYPTMEEFRNFSRYIAYIESQG
AHRAGLAKVVPPKEWKPRASYDDIDDLVIPAPIQQLVTGQSGLFTQYNIQKKAMTVREFR
KIANSDKYCTPRYSEFEELERKYWKNLTFNPPIYGADVNGTLYEKHVDEWNIGRLRTILD
LVEKESGITIEGVNTPYLYFGMWKTSFAWHTEDMDLYSINYLHFGEPKSWYSVPPEHGKR
LERLAKGFFPGSAQSCEAFLRHKMTLISPLMLKKYGIPFDKVTQEAGEFMITFPYGYHAG
FNHGFNCAESTNFATRRWIEYGKQAVLCSCRKDMVKISMDVFVRKFQPERYKLWKAGKDN
TVIDHTLPTPEAAEFLKESEL
Sequence of entity 2 (C, D), FASTA
>2YBP_2 HISTONE H3.1T (chains C, D)
PATGGVKKPHRY

Ligands and cofactors

IDNameFormulaCopies
2HG(2R)-2-hydroxypentanedioic acidC5 H8 O52
ZNZinc ionZn2
NINickel (II) ionNi2

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

Primary citation

The oncometabolite 2-hydroxyglutarate inhibits histone lysine demethylases. Chowdhury, R., Yeoh, K.K., Tian, Y.M. et al. EMBO Rep (2011) 12:463-469. DOI 10.1038/embor.2011.43 · 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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