Chlorine in PDB 5ttg: Crystal Structure of Catalytic Domain of Glp with MS012

All present enzymatic activity of Crystal Structure of Catalytic Domain of Glp with MS012:
2.1.1.43;

The structure of Crystal Structure of Catalytic Domain of Glp with MS012, PDB code: 5ttg was solved by A.Dong, H.Zeng, J.Liu, Y.Xiong, N.Babault, J.Jin, W.Tempel, C.Bountra, C.H.Arrowsmith, A.M.Edwards, H.Wu, P.J.Brown, Structural Genomicsconsortium (Sgc), with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	50.01 / 1.66
Space group	P 21 21 21
Cell size a, b, c (Å), α, β, γ (°)	74.429, 95.900, 102.113, 90.00, 90.00, 90.00
R / Rfree (%)	17.1 / 19.2

The structure of Crystal Structure of Catalytic Domain of Glp with MS012 also contains other interesting chemical elements:

Zinc

(Zn)

8 atoms

The binding sites of Chlorine atom in the Crystal Structure of Catalytic Domain of Glp with MS012 (pdb code 5ttg). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total only one binding site of Chlorine was determined in the Crystal Structure of Catalytic Domain of Glp with MS012, PDB code: 5ttg:

Chlorine binding site 1 out of 1 in the Crystal Structure of Catalytic Domain of Glp with MS012


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Crystal Structure of Catalytic Domain of Glp with MS012 within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl1307 b:19.6 occ:1.00 ND2 A:ASN1122 3.2 14.6 1.0 NH2 A:ARG1125 3.3 14.6 1.0 O A:HOH1525 3.5 12.5 1.0 CA A:VAL1119 3.6 13.3 1.0 NE A:ARG1125 3.6 14.0 1.0 O A:ARG1118 3.7 15.4 1.0 O A:HOH1682 3.8 16.3 1.0 CB A:ASN1122 3.8 14.0 1.0 O A:VAL1119 3.9 12.6 1.0 CZ A:ARG1125 3.9 14.1 1.0 CG A:ASN1122 4.0 14.6 1.0 CG1 A:VAL1119 4.2 14.0 1.0 C A:VAL1119 4.2 12.4 1.0 CB A:VAL1119 4.2 13.6 1.0 CG2 A:VAL1119 4.3 13.7 1.0 C A:ARG1118 4.5 14.3 1.0 N A:VAL1119 4.5 13.6 1.0 CD A:ARG1125 4.8 14.2 1.0

Y.Xiong, F.Li, N.Babault, A.Dong, H.Zeng, H.Wu, X.Chen, C.H.Arrowsmith, P.J.Brown, J.Liu, M.Vedadi, J.Jin. Discovery of Potent and Selective Inhibitors For G9A-Like Protein (Glp) Lysine Methyltransferase. J. Med. Chem. V. 60 1876 2017.
ISSN: ISSN 1520-4804
PubMed: 28135087
DOI: 10.1021/ACS.JMEDCHEM.6B01645