Chlorine in PDB 5fu8: Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor

All present enzymatic activity of Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor:
2.7.7.24;

The structure of Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor, PDB code: 5fu8 was solved by M.S.Alphey, F.Tran, N.J.Westwood, J.H.Naismith, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	134.64 / 2.20
Space group	C 1 2 1
Cell size a, b, c (Å), α, β, γ (°)	64.180, 154.480, 134.750, 90.00, 92.34, 90.00
R / Rfree (%)	20 / 24.9

The structure of Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor also contains other interesting chemical elements:

Bromine

(Br)

4 atoms

The binding sites of Chlorine atom in the Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor (pdb code 5fu8). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 4 binding sites of Chlorine where determined in the Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor, PDB code: 5fu8:
Jump to Chlorine binding site number: 1; 2; 3; 4;

Chlorine binding site 1 out of 4 in the Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 1 of Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor within 5.0Å range: probe atom residue distance (Å) B Occ A:Cl3001 b:30.9 occ:1.00 ND1 A:HIS116 2.9 17.2 1.0 O A:HOH2076 3.0 35.3 1.0 O A:HOH2074 3.5 17.7 1.0 CG A:HIS116 3.8 16.0 1.0 CA A:HIS116 3.8 15.4 1.0 CE1 A:HIS116 3.8 17.1 1.0 CB A:HIS116 3.9 16.0 1.0 O A:HOH2182 4.0 14.6 1.0 N A:ASP117 4.3 17.8 1.0 C A:HIS116 4.6 16.4 1.0 N A:HIS116 4.8 14.2 1.0 CD2 A:HIS116 4.9 16.3 1.0 NE2 A:HIS116 4.9 17.2 1.0 O A:GLY115 5.0 12.4 1.0

Chlorine binding site 2 out of 4 in the Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor within 5.0Å range: probe atom residue distance (Å) B Occ B:Cl3001 b:32.5 occ:1.00 ND1 B:HIS116 3.0 17.4 1.0 O B:HOH2060 3.3 19.2 1.0 CA B:HIS116 3.7 18.5 1.0 CG B:HIS116 3.9 17.8 1.0 CE1 B:HIS116 3.9 17.2 1.0 O B:HOH2153 3.9 14.8 1.0 CB B:HIS116 4.0 17.9 1.0 N B:ASP117 4.2 22.2 1.0 C B:HIS116 4.6 19.6 1.0 N B:HIS116 4.7 17.5 1.0 O B:GLY115 4.9 16.2 1.0 NE2 B:HIS116 5.0 17.3 1.0

Chlorine binding site 3 out of 4 in the Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor within 5.0Å range: probe atom residue distance (Å) B Occ C:Cl3001 b:37.8 occ:1.00 ND1 C:HIS116 2.9 18.8 1.0 O C:HOH2066 2.9 16.8 1.0 O C:HOH2158 3.5 20.2 1.0 O C:HOH2062 3.6 9.7 1.0 CA C:HIS116 3.8 15.9 1.0 CE1 C:HIS116 3.8 19.6 1.0 CG C:HIS116 3.8 18.2 1.0 CB C:HIS116 4.0 16.9 1.0 N C:ASP117 4.2 17.4 1.0 C C:HIS116 4.5 16.9 1.0 N C:HIS116 4.8 14.1 1.0 NE2 C:HIS116 4.9 19.3 1.0 O C:GLY115 4.9 12.8 1.0 CD2 C:HIS116 5.0 18.6 1.0

Chlorine binding site 4 out of 4 in the Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 4 of Pseudomonas Aeruginosa Rmla in Complex with Allosteric Inhibitor within 5.0Å range: probe atom residue distance (Å) B Occ D:Cl3001 b:41.4 occ:1.00 ND1 D:HIS116 2.8 21.2 1.0 O D:HOH2060 3.2 25.5 1.0 O D:HOH2057 3.5 25.2 1.0 CA D:HIS116 3.6 20.5 1.0 CG D:HIS116 3.7 21.1 1.0 CE1 D:HIS116 3.7 21.5 1.0 O D:HOH2149 3.9 12.0 1.0 CB D:HIS116 3.9 20.6 1.0 O D:HOH2148 4.0 19.9 1.0 N D:ASP117 4.1 23.8 1.0 C D:HIS116 4.4 22.0 1.0 N D:HIS116 4.6 19.2 1.0 O D:HOH2061 4.8 36.1 1.0 O D:GLY115 4.8 16.6 1.0 NE2 D:HIS116 4.9 22.0 1.0 CD2 D:HIS116 4.9 21.3 1.0

F.Tran, M.S.Alphey, N.J.Westwood, J.H.Naismith. Allosteric Competitive Inhibitors of the Glucose-1-Phosphate Thymidylyltransferase (Rmla) From Pseudomonas Aeruginosa. To Be Published.