Bromine in PDB 6uoz: Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction

The structure of Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction, PDB code: 6uoz was solved by B.Zhao, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	27.53 / 1.53
Space group	P 1
Cell size a, b, c (Å), α, β, γ (°)	46.711, 56.948, 64.924, 108.36, 90.76, 114.17
R / Rfree (%)	14.3 / 16.9

The structure of Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction also contains other interesting chemical elements:

Chlorine

(Cl)

2 atoms

The binding sites of Bromine atom in the Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction (pdb code 6uoz). This binding sites where shown within 5.0 Angstroms radius around Bromine atom.
In total 2 binding sites of Bromine where determined in the Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction, PDB code: 6uoz:
Jump to Bromine binding site number: 1; 2;

Bromine binding site 1 out of 2 in the Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction


Mono view


Stereo pair view

A full contact list of Bromine with other atoms in the Br binding site number 1 of Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction within 5.0Å range: probe atom residue distance (Å) B Occ A:Br401 b:22.4 occ:1.00 BR01 A:QF1401 0.0 22.4 1.0 C02 A:QF1401 1.9 20.2 1.0 C03 A:QF1401 2.8 19.9 1.0 C01 A:QF1401 2.8 21.0 1.0 O A:TRP273 3.3 12.9 1.0 O A:SER267 3.6 17.8 1.0 N A:TRP273 3.7 14.9 1.0 CD2 A:PHE266 3.8 14.0 1.0 CB A:LYS272 3.8 17.3 1.0 C A:LYS272 3.8 17.3 1.0 CA A:LYS272 3.9 16.4 1.0 CB A:PHE266 3.9 13.8 1.0 C A:TRP273 4.0 15.0 1.0 N A:SER267 4.0 11.9 1.0 CD2 A:LEU288 4.1 21.6 1.0 C06 A:QF1401 4.1 28.4 1.0 C04 A:QF1401 4.1 22.5 1.0 CD1 A:LEU288 4.2 18.6 1.0 CA A:PHE266 4.2 11.1 1.0 C A:SER267 4.3 13.7 1.0 CG A:PHE266 4.4 13.4 1.0 CB A:LEU288 4.4 19.3 1.0 CG A:LEU288 4.4 20.5 1.0 CA A:TRP273 4.4 15.1 1.0 C A:PHE266 4.5 14.1 1.0 CG A:LYS272 4.5 22.2 1.0 O A:LYS272 4.6 18.7 1.0 C05 A:QF1401 4.6 26.7 1.0 CD1 A:ILE274 4.7 12.5 1.0 CG1 A:VAL268 4.8 20.3 1.0 CA A:SER267 4.9 14.0 1.0 CE2 A:PHE266 4.9 16.0 1.0 N A:ILE274 5.0 12.2 1.0

Bromine binding site 2 out of 2 in the Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction


Mono view


Stereo pair view

A full contact list of Bromine with other atoms in the Br binding site number 2 of Discovery of Fragment-Inspired Heterocyclic Benzenesulfonmides As Inhibitors of the WDR5-Myc Interaction within 5.0Å range: probe atom residue distance (Å) B Occ B:Br401 b:21.4 occ:1.00 BR01 B:QF1401 0.0 21.4 1.0 C02 B:QF1401 1.9 19.5 1.0 C01 B:QF1401 2.8 24.7 1.0 C03 B:QF1401 2.8 15.9 1.0 O B:TRP273 3.2 14.0 1.0 O B:SER267 3.6 17.4 1.0 N B:TRP273 3.6 11.9 1.0 CB B:PHE266 3.8 11.4 1.0 CD2 B:PHE266 3.8 12.7 1.0 C B:LYS272 3.9 14.1 1.0 N B:SER267 3.9 10.9 1.0 CB B:LYS272 3.9 24.3 1.0 CA B:LYS272 3.9 16.0 1.0 C B:TRP273 3.9 13.3 1.0 CD2 B:LEU288 4.1 15.8 1.0 C06 B:QF1401 4.1 27.4 1.0 C04 B:QF1401 4.1 17.6 1.0 CA B:PHE266 4.1 10.9 1.0 CD1 B:LEU288 4.2 16.0 1.0 C B:SER267 4.3 14.3 1.0 C B:PHE266 4.3 14.8 1.0 CG B:PHE266 4.4 12.1 1.0 CA B:TRP273 4.4 12.5 1.0 CB B:LEU288 4.4 15.2 1.0 CG B:LEU288 4.4 15.1 1.0 O B:LYS272 4.6 13.6 1.0 C05 B:QF1401 4.6 19.7 1.0 CG B:LYS272 4.7 25.4 1.0 CD1 B:ILE274 4.7 15.6 1.0 CA B:SER267 4.8 12.4 1.0 N B:ILE274 4.9 10.9 1.0 CE2 B:PHE266 5.0 13.8 1.0

S.Chacon Simon, F.Wang, L.R.Thomas, J.Phan, B.Zhao, E.T.Olejniczak, J.D.Macdonald, J.G.Shaw, C.Schlund, W.G.Payne, J.Creighton, S.Stauffer, A.G.Waterson, W.P.Tansey, S.W.Fesik. Discovery of Wd Repeat-Containing Protein 5 (WDR5)-Myc Inhibitors Using Fragment-Based Methods and Structure-Based Design. J.Med.Chem. 2020.
ISSN: ISSN 0022-2623
PubMed: 32223236
DOI: 10.1021/ACS.JMEDCHEM.0C00224