Chlorine in PDB 5ly1: JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer)

The structure of JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer), PDB code: 5ly1 was solved by O.N.F.King, R.Chowdhury, A.Kawamura, C.J.Schofield, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	49.34 / 2.50
Space group	P 1 21 1
Cell size a, b, c (Å), α, β, γ (°)	57.265, 101.482, 140.330, 90.00, 99.56, 90.00
R / Rfree (%)	17.8 / 20.5

The structure of JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer) also contains other interesting chemical elements:

Nickel	(Ni)	4 atoms
Zinc	(Zn)	4 atoms

The binding sites of Chlorine atom in the JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer) (pdb code 5ly1). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 3 binding sites of Chlorine where determined in the JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer), PDB code: 5ly1:
Jump to Chlorine binding site number: 1; 2; 3;

Chlorine binding site 1 out of 3 in the JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer)


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer) within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl503 b:74.3 occ:1.00 N A:GLY229 3.3 62.1 1.0 C A:PHE227 3.5 61.4 1.0 CA A:PHE227 3.5 60.1 1.0 CE B:LYS105 3.6 75.4 1.0 N A:PRO228 3.7 60.1 1.0 CD A:PRO228 3.8 59.2 1.0 CA A:GLY229 3.8 62.1 1.0 N A:SER230 3.9 58.5 1.0 NZ B:LYS105 4.0 73.7 1.0 O A:PHE227 4.0 62.7 1.0 CB A:PHE227 4.1 59.0 1.0 CD B:LYS105 4.2 76.2 1.0 CG A:PRO228 4.3 60.4 1.0 C A:PRO228 4.3 60.2 1.0 C A:GLY229 4.4 60.4 1.0 OG A:SER230 4.5 59.1 1.0 CD1 A:PHE227 4.5 57.1 1.0 CA A:PRO228 4.5 60.2 1.0 O A:PHE226 4.6 55.8 1.0 N A:PHE227 4.8 58.2 1.0 CG A:PHE227 4.8 57.7 1.0 CB A:SER230 5.0 57.8 1.0

Chlorine binding site 2 out of 3 in the JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer)


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer) within 5.0Å range: probe atom residue distance (Å) B Occ C:Cl404 b:66.2 occ:1.00 N C:GLY229 3.1 51.2 1.0 N C:SER230 3.4 45.8 1.0 NZ D:LYS105 3.5 76.7 1.0 CA C:PHE227 3.5 43.1 1.0 C C:PHE227 3.5 45.7 1.0 CA C:GLY229 3.5 50.9 1.0 OG C:SER230 3.6 44.5 1.0 CB C:PHE227 3.8 39.7 1.0 O C:PHE227 3.9 43.1 1.0 N C:PRO228 3.9 48.9 1.0 C C:GLY229 3.9 49.9 1.0 CD D:LYS105 4.0 76.4 1.0 CE D:LYS105 4.1 76.1 1.0 C C:PRO228 4.2 50.9 1.0 CD C:PRO228 4.3 50.6 1.0 CB C:SER230 4.4 44.3 1.0 CD1 C:PHE227 4.4 36.1 1.0 CA C:SER230 4.5 44.3 1.0 CG C:PHE227 4.6 37.4 1.0 CA C:PRO228 4.6 50.7 1.0 CG C:PRO228 4.8 51.5 1.0 N C:PHE227 4.8 46.2 1.0 O C:PHE226 4.9 51.2 1.0

Chlorine binding site 3 out of 3 in the JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer)


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of JMJD2A/ KDM4A Complexed with Ni(II) and Macrocyclic Peptide Inhibitor CP2 (13-Mer) within 5.0Å range: probe atom residue distance (Å) B Occ D:Cl503 b:80.2 occ:1.00 N D:GLY229 2.8 50.6 1.0 CA D:GLY229 3.3 54.1 1.0 C D:PHE227 3.4 41.3 1.0 N D:SER230 3.5 55.2 1.0 N D:PRO228 3.5 42.1 1.0 CA D:PHE227 3.6 40.3 1.0 CD D:PRO228 3.8 41.1 1.0 C D:GLY229 3.9 56.8 1.0 C D:PRO228 3.9 46.3 1.0 O D:PHE227 3.9 41.6 1.0 OG D:SER230 4.1 53.9 1.0 CB D:PHE227 4.2 39.1 1.0 CG D:PRO228 4.3 41.5 1.0 CA D:PRO228 4.3 43.4 1.0 CD1 D:PHE227 4.7 38.3 1.0 CA D:SER230 4.7 54.4 1.0 CB D:SER230 4.7 54.2 1.0 CE C:LYS105 4.8 78.4 1.0 N D:PHE227 4.9 41.6 1.0 O D:PHE226 4.9 49.1 1.0 CG D:PHE227 4.9 38.4 1.0 CB D:PRO228 4.9 42.3 1.0 O D:PRO228 5.0 45.4 1.0

A.Kawamura, M.Munzel, T.Kojima, C.Yapp, B.Bhushan, Y.Goto, A.Tumber, T.Katoh, O.N.King, T.Passioura, L.J.Walport, S.B.Hatch, S.Madden, S.Muller, P.E.Brennan, R.Chowdhury, R.J.Hopkinson, H.Suga, C.J.Schofield. Highly Selective Inhibition of Histone Demethylases By De Novo Macrocyclic Peptides. Nat Commun V. 8 14773 2017.
ISSN: ESSN 2041-1723
PubMed: 28382930
DOI: 10.1038/NCOMMS14773