6G5X: KDM4A with compound YP-02-145

Crystal Structure of KDM4A with compound YP-02-145. Determined by X-ray diffraction at 1.78 Å resolution. Released 10 Apr 2019.

Method
X-ray diffraction
Resolution
1.78 Å
Organism
Homo sapiens
Chains
2
Atoms
6,389
Mol. weight
85.15 kDa
Ligands
MY7, CIT, NI, ZN
Released
10 Apr 2019

Explore 6G5X in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6G5X contains 48 α-helices and 34 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: 25 helices, 17 β-strands

ElementResiduesLengthSheet
α-helix4-74
α-helix13-153
β-strand16-1721
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-helix94-1029
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-helix189-1902
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
α-helix2631
β-strand267-27041
β-strand275-28064
β-strand284-29181
α-helix296-3027
α-helix303-3064
α-helix318-3247
α-helix326-3283
α-helix329-3335
α-helix345-3473
α-helix348-3525
Chain B: 23 helices, 17 β-strands
ElementResiduesLengthSheet
α-helix13-153
β-strand16-1725
α-helix21-244
α-helix27-3610
α-helix39-424
β-strand44-4745
α-helix48-503
β-strand66-6726
β-strand71-7887
β-strand81-8887
β-strand92-9326
α-helix94-1029
α-helix108-1103
α-helix114-12411
β-strand131-13227
β-strand133-13755
α-helix156-1583
α-helix159-1646
β-strand175-17955
β-strand184-18858
α-helix189-1902
α-helix191-1933
β-strand195-20395
β-strand206-21168
α-helix213-2153
α-helix216-22611
α-helix228-2336
α-helix237-2404
β-strand243-24537
α-helix247-2526
β-strand258-26258
α-helix2631
β-strand267-27045
β-strand275-28068
β-strand284-29185
α-helix296-3027
α-helix318-3247
α-helix329-3335
α-helix345-3473
α-helix348-3536

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Lysine-specific demethylase 4AA, Bprotein359Homo sapiensO75164 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>6G5X_1 Lysine-specific demethylase 4A (chains A, B)
MASESETLNPSARIMTFYPTMEEFRNFSRYIAYIESQGAHRAGLAKVVPPKEWKPRASYD
DIDDLVIPAPIQQLVTGQSGLFTQYNIQKKAMTVREFRKIANSDKYCTPRYSEFEELERK
YWKNLTFNPPIYGADVNGTLYEKHVDEWNIGRLRTILDLVEKESGITIEGVNTPYLYFGM
WKTSFAWHTEDMDLYSINYLHFGEPKSWYSVPPEHGKRLERLAKGFFPGSAQSCEAFLRH
KMTLISPLMLKKYGIPFDKVTQEAGEFMITFPYGYHAGFNHGFNCAESTNFATRRWIEYG
KQAVLCSCRKDMVKISMDVFVRKFQPERYKLWKAGKDNTVIDHTLPTPEAAEFLKESEL

Ligands and cofactors

IDNameFormulaCopies
MY72-(3-methyl-5-oxidanylidene-4-phenyl-4~{H}-pyrazol-1-yl)-3~{H}-benzimidazole-5-…C18 H14 N4 O31
CITCitric acidC6 H8 O73
NINickel (II) ionNi4
ZNZinc ionZn2

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

Primary citation

Enhanced Properties of a Benzimidazole Benzylpyrazole Lysine Demethylase Inhibitor: Mechanism-of-Action, Binding Site Analysis, and Activity in Cellular Models of Prostate Cancer. Carter, D.M., Specker, E., Malecki, P.H. et al. J Med Chem (2021) 64:14266-14282. DOI 10.1021/acs.jmedchem.1c00693 · 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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