5ANQ: Lysine-specific demethylase 4A

inhibitors of JumonjiC domain-containing histone demethylases. Determined by X-ray diffraction at 2.0 Å resolution. Released 23 Mar 2016.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
HOMO SAPIENS
Chains
2
Atoms
6,125
Mol. weight
84.92 kDa
Ligands
5YQ, FE2, ZN
Released
23 Mar 2016

Explore 5ANQ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5ANQ 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-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-helix94-1029
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-helix339-3413
α-helix346-3472
α-helix348-3503
Chain B: 23 helices, 17 β-strands
ElementResiduesLengthSheet
α-helix141
β-strand15-1735
α-helix21-255
α-helix27-3610
α-helix39-424
β-strand44-4745
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-helix156-1605
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-helix303-3064
α-helix318-3247
α-helix326-3338
α-helix339-3413
α-helix346-3472
α-helix348-3525

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Lysine-specific demethylase 4AA, Bprotein359HOMO SAPIENSO75164 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5ANQ_1 LYSINE-SPECIFIC DEMETHYLASE 4A (chains A, B)
MASESETLNPSARIMTFYPTMEEFRNFSRYIAYIESQGAHRAGLAKVVPPKEWKPRASYD
DIDDLVIPAPIQQLVTGQSGLFTQYNIQKKAMTVREFRKIANSDKYCTPRYSEFEELERK
YWKNLTFNPPIYGADVNGTLYEKHVDEWNIGRLRTILDLVEKESGITIEGVNTPYLYFGM
WKTSFAWHTEDMDLYSINYLHFGEPKSWYSVPPEHGKRLERLAKGFFPGSAQSCEAFLRH
KMTLISPLMLKKYGIPFDKVTQEAGEFMITFPYGYHAGFNHGFNCAESTNFATRRWIEYG
KQAVLCSCRKDMVKISMDVFVRKFQPERYKLWKAGKDNTVIDHTLPTPEAAEFLKESEL

Ligands and cofactors

IDNameFormulaCopies
5YQ2-{2-[(pyridin-3-ylmethyl)amino]pyrimidin-4-yl}pyridine-4-carboxylic acidC16 H13 N5 O22
FE2FE (II) ionFe2
ZNZinc ionZn2

Water and common crystallization additives (SO4, CL) are not listed.

Primary citation

Substituted 2-(2-Aminopyrimidin-4-Yl)Pyridine-4-Carboxylates as Potent Inhibitors of Jumonjic Domain-Containing Histone Demethylases. Roatsch, M., Robaa, D., Pippel, M. et al. Future Med Chem (2016) 8:1553. DOI 10.4155/FMC.15.188 · 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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