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Chlorine in PDB 5syj: Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid

Enzymatic activity of Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid

All present enzymatic activity of Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid:
1.11.1.21;

Protein crystallography data

The structure of Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid, PDB code: 5syj was solved by P.C.Loewen, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 1.88
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 100.640, 114.640, 174.990, 90.00, 90.00, 90.00
R / Rfree (%) 14 / 17

Other elements in 5syj:

The structure of Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid also contains other interesting chemical elements:

Iron (Fe) 2 atoms
Sodium (Na) 2 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid (pdb code 5syj). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 2 binding sites of Chlorine where determined in the Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid, PDB code: 5syj:
Jump to Chlorine binding site number: 1; 2;

Chlorine binding site 1 out of 2 in 5syj

Go back to Chlorine Binding Sites List in 5syj
Chlorine binding site 1 out of 2 in the Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid


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 the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl803

b:35.3
occ:1.00
O A:HOH1368 2.9 20.7 1.0
O A:HOH1451 3.2 24.1 1.0
O A:HOH1406 3.2 24.3 1.0
N A:GLY124 3.2 20.4 1.0
CG2 A:VAL200 3.5 29.4 1.0
N3 A:NIZ809 3.6 45.1 1.0
CG A:GLU198 3.6 42.0 1.0
CB A:GLU198 3.8 40.0 1.0
N2 A:NIZ809 3.9 52.1 1.0
CA A:GLY124 4.0 21.1 1.0
CB A:ARG123 4.2 21.4 1.0
C A:ARG123 4.3 22.2 1.0
CA A:ARG123 4.3 19.9 1.0
CD A:GLU198 4.3 44.5 1.0
OE1 A:GLU128 4.5 28.9 1.0
NA A:NA802 4.5 21.6 1.0
OE1 A:GLU198 4.6 41.3 1.0
CG A:ARG123 4.7 21.6 1.0
OE2 A:GLU128 4.7 33.2 1.0
O A:GLY124 4.7 21.9 1.0
C A:GLY124 4.7 21.2 1.0
CD A:GLU128 4.8 29.8 1.0
CB A:VAL200 4.9 28.4 1.0
O A:HOH1268 5.0 25.6 1.0

Chlorine binding site 2 out of 2 in 5syj

Go back to Chlorine Binding Sites List in 5syj
Chlorine binding site 2 out of 2 in the Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 2 of Crystal Structure of the D141A Variant of B. Pseudomallei Katgin Complex with Isoniazid within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl803

b:30.4
occ:1.00
O B:HOH1345 3.1 20.9 1.0
O B:HOH1457 3.1 19.1 1.0
O B:HOH1418 3.2 24.3 1.0
N B:GLY124 3.2 19.9 1.0
N3 B:NIZ809 3.5 37.9 1.0
CG2 B:VAL200 3.5 26.0 1.0
CG B:GLU198 3.6 34.6 1.0
N2 B:NIZ809 3.7 40.3 1.0
CB B:GLU198 3.8 33.0 1.0
CA B:GLY124 3.9 17.6 1.0
CB B:ARG123 4.2 18.2 1.0
CD B:GLU198 4.3 37.7 1.0
C B:ARG123 4.3 19.3 1.0
CA B:ARG123 4.3 18.9 1.0
OE1 B:GLU128 4.4 27.8 1.0
OE1 B:GLU198 4.5 37.7 1.0
OE2 B:GLU128 4.6 30.2 1.0
NA B:NA802 4.6 20.2 1.0
CD B:GLU128 4.7 25.1 1.0
C B:GLY124 4.7 17.6 1.0
O B:GLY124 4.7 18.2 1.0
CG B:ARG123 4.8 18.9 1.0
C B:NIZ809 4.9 41.1 1.0
O B:HOH1205 4.9 23.1 1.0
CB B:VAL200 4.9 24.5 1.0
CG B:GLN130 4.9 19.5 1.0

Reference:

P.Vidossich, P.C.Loewen, X.Carpena, G.Fiorin, I.Fita, C.Rovira. Binding of the Antitubercular Pro-Drug Isoniazid in the Heme Access Channel of Catalase-Peroxidase (Katg). A Combined Structural and Metadynamics Investigation. J Phys Chem B V. 118 2924 2014.
ISSN: ISSN 1520-5207
PubMed: 24568093
DOI: 10.1021/JP4123425
Page generated: Sat Jul 12 08:41:52 2025

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