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Chlorine in PDB 6v59: Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264

Protein crystallography data

The structure of Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264, PDB code: 6v59 was solved by S.E.Cohen, C.L.Drennan, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 48.23 / 1.59
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 49.970, 87.605, 184.170, 90.00, 90.00, 90.00
R / Rfree (%) 15.1 / 17.7

Other elements in 6v59:

The structure of Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264 also contains other interesting chemical elements:

Magnesium (Mg) 1 atom
Iron (Fe) 4 atoms

Chlorine Binding Sites:

The binding sites of Chlorine atom in the Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264 (pdb code 6v59). This binding sites where shown within 5.0 Angstroms radius around Chlorine atom.
In total 4 binding sites of Chlorine where determined in the Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264, PDB code: 6v59:
Jump to Chlorine binding site number: 1; 2; 3; 4;

Chlorine binding site 1 out of 4 in 6v59

Go back to Chlorine Binding Sites List in 6v59
Chlorine binding site 1 out of 4 in the Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264


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 Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl607

b:18.3
occ:1.00
HB1 B:ALA205 2.9 20.8 1.0
HB1 A:ALA205 3.0 23.3 1.0
O A:HOH864 3.0 18.4 1.0
HZ B:PHE221 3.0 22.7 1.0
HZ A:PHE221 3.1 19.5 1.0
O B:HOH801 3.1 20.6 1.0
O A:HOH903 3.1 20.0 1.0
O B:HOH924 3.2 22.3 1.0
HA2 A:GLY219 3.6 23.0 1.0
HA2 B:GLY219 3.6 21.0 1.0
HE2 B:PHE221 3.7 20.8 1.0
CB B:ALA205 3.8 17.3 1.0
CZ B:PHE221 3.9 18.9 1.0
HE1 A:PHE221 3.9 20.5 1.0
CB A:ALA205 3.9 19.4 1.0
CZ A:PHE221 3.9 16.2 1.0
H A:GLY219 4.1 21.4 1.0
HB2 B:ALA205 4.1 20.8 1.0
HB2 A:ALA205 4.1 23.3 1.0
H B:GLY219 4.2 21.0 1.0
CE2 B:PHE221 4.2 17.4 1.0
HB3 B:ALA205 4.2 20.8 1.0
CE1 A:PHE221 4.3 17.1 1.0
HB3 A:ALA205 4.3 23.3 1.0
CA A:GLY219 4.4 19.1 1.0
CA B:GLY219 4.5 17.5 1.0
N A:GLY219 4.6 17.9 1.0
N B:GLY219 4.7 17.5 1.0
HA B:ALA205 4.8 17.8 1.0
HA3 A:GLY219 4.8 23.0 1.0
HA A:ALA205 4.8 20.4 1.0
HA3 B:GLY219 4.8 21.0 1.0
CA B:ALA205 4.8 14.8 1.0
O B:ALA205 4.8 15.9 1.0
O A:ALA205 4.8 17.6 1.0
CA A:ALA205 4.8 17.0 1.0

Chlorine binding site 2 out of 4 in 6v59

Go back to Chlorine Binding Sites List in 6v59
Chlorine binding site 2 out of 4 in the Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264


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 Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Cl608

b:46.4
occ:1.00
H A:SER378 2.7 30.4 1.0
HB1 A:ALA377 2.8 39.5 1.0
H A:ARG379 3.0 33.5 1.0
HG3 A:ARG379 3.2 38.5 1.0
HB2 A:ARG379 3.2 35.4 1.0
N A:SER378 3.5 25.4 1.0
CB A:ALA377 3.7 32.9 1.0
N A:ARG379 3.7 28.0 1.0
OG A:SER378 3.7 39.2 1.0
HA A:ALA377 3.7 32.5 1.0
CG A:ARG379 3.8 32.0 1.0
HD3 A:ARG382 3.8 35.5 1.0
HD2 A:ARG382 3.8 35.5 1.0
HG3 A:ARG382 3.8 35.2 1.0
CB A:ARG379 3.9 29.5 1.0
HB2 A:ALA377 3.9 39.5 1.0
CD A:ARG379 3.9 33.9 1.0
HD3 A:ARG379 4.0 40.7 1.0
CA A:ALA377 4.1 27.1 1.0
CD A:ARG382 4.2 29.6 1.0
HG A:SER378 4.2 47.1 1.0
C A:ALA377 4.3 34.0 1.0
CA A:SER378 4.4 24.3 1.0
HB3 A:ALA377 4.4 39.5 1.0
C A:SER378 4.4 29.4 1.0
CA A:ARG379 4.4 26.9 1.0
CG A:ARG382 4.5 29.3 1.0
CB A:SER378 4.6 34.0 1.0
HG2 A:ARG379 4.7 38.5 1.0
HB3 A:ARG379 4.7 35.4 1.0
HD2 A:ARG379 4.9 40.7 1.0
HB3 A:SER378 4.9 40.8 1.0

Chlorine binding site 3 out of 4 in 6v59

Go back to Chlorine Binding Sites List in 6v59
Chlorine binding site 3 out of 4 in the Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 3 of Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl610

b:50.2
occ:1.00
HE B:ARG379 2.4 58.5 1.0
HB1 B:ALA377 2.8 30.1 1.0
HH11 B:ARG382 2.8 68.4 1.0
HH21 B:ARG379 2.9 69.7 1.0
H B:ARG379 3.1 29.7 1.0
H B:SER378 3.1 35.7 1.0
HH12 B:ARG382 3.2 68.4 1.0
NE B:ARG379 3.3 48.7 1.0
NH1 B:ARG382 3.3 57.0 1.0
HG3 B:ARG382 3.3 38.3 1.0
HB2 B:ARG379 3.3 29.5 1.0
HG3 B:ARG379 3.6 37.5 1.0
NH2 B:ARG379 3.6 58.1 1.0
CB B:ALA377 3.7 25.0 1.0
N B:SER378 3.7 29.8 1.0
HA B:ALA377 3.7 26.7 1.0
N B:ARG379 3.8 24.7 1.0
OG B:SER378 3.8 43.1 1.0
CZ B:ARG379 3.9 54.0 1.0
HB2 B:ALA377 4.0 30.1 1.0
CB B:ARG379 4.1 24.6 1.0
CA B:ALA377 4.1 22.3 1.0
CG B:ARG379 4.1 31.2 1.0
CG B:ARG382 4.2 31.9 1.0
C B:ALA377 4.3 30.1 1.0
CD B:ARG379 4.3 35.5 1.0
HG B:SER378 4.3 51.7 1.0
HD3 B:ARG382 4.3 46.9 1.0
HB3 B:ALA377 4.4 30.1 1.0
HH22 B:ARG379 4.4 69.7 1.0
CZ B:ARG382 4.4 55.3 1.0
HG2 B:ARG382 4.5 38.3 1.0
CA B:SER378 4.5 30.7 1.0
CA B:ARG379 4.6 23.5 1.0
C B:SER378 4.6 31.8 1.0
CD B:ARG382 4.7 39.1 1.0
CB B:SER378 4.8 34.8 1.0
HD3 B:ARG379 4.8 42.6 1.0
HB3 B:ARG379 4.9 29.5 1.0
NE B:ARG382 5.0 43.6 1.0

Chlorine binding site 4 out of 4 in 6v59

Go back to Chlorine Binding Sites List in 6v59
Chlorine binding site 4 out of 4 in the Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264


Mono view


Stereo pair view

A full contact list of Chlorine with other atoms in the Cl binding site number 4 of Crystal Structure of the Diheme Peroxidase Btha Y463M Variant From Burkholderia Thailandensis E264 within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Cl611

b:24.6
occ:1.00
H B:LYS539 2.5 27.9 1.0
HD3 B:LYS539 2.9 26.4 1.0
O B:HOH934 3.1 26.5 1.0
HB2 B:LYS539 3.2 22.9 1.0
HG3 B:LYS539 3.2 22.6 1.0
N B:LYS539 3.3 23.2 1.0
HA2 B:GLY538 3.4 24.7 1.0
HA3 B:GLY538 3.6 24.7 1.0
CD B:LYS539 3.7 22.0 1.0
CG B:LYS539 3.7 18.9 1.0
CB B:LYS539 3.8 19.1 1.0
CA B:GLY538 3.9 20.6 1.0
HD2 B:LYS539 4.1 26.4 1.0
C B:GLY538 4.1 24.4 1.0
CA B:LYS539 4.1 20.3 1.0
HG2 B:LYS539 4.6 22.6 1.0
HB3 B:LYS539 4.7 22.9 1.0
HG22 B:THR455 4.8 21.9 1.0
O B:LYS539 4.8 22.6 1.0
HA B:LYS539 4.9 24.4 1.0
CE B:LYS539 4.9 25.2 1.0
HE3 B:LYS539 5.0 30.2 1.0

Reference:

K.Rizzolo, A.C.Weitz, S.E.Cohen, C.L.Drennan, M.P.Hendrich, S.J.Elliott. A Stable Ferryl Porphyrin at the Active Site of Y463M Btha. J.Am.Chem.Soc. V. 142 11978 2020.
ISSN: ESSN 1520-5126
PubMed: 32564595
DOI: 10.1021/JACS.0C04023
Page generated: Sat Jul 12 20:44:23 2025

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