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Iron in PDB 5syv: Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant

Enzymatic activity of Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant

All present enzymatic activity of Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant:
1.11.1.21;

Protein crystallography data

The structure of Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant, PDB code: 5syv 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) 48.00 / 1.75
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 100.792, 113.296, 174.520, 90.00, 90.00, 90.00
R / Rfree (%) 15.9 / 19

Other elements in 5syv:

The structure of Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant also contains other interesting chemical elements:

Chlorine (Cl) 2 atoms
Sodium (Na) 2 atoms

Iron Binding Sites:

The binding sites of Iron atom in the Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant (pdb code 5syv). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant, PDB code: 5syv:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 5syv

Go back to Iron Binding Sites List in 5syv
Iron binding site 1 out of 2 in the Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe801

b:12.0
occ:1.00
FE A:HEM801 0.0 12.0 1.0
ND A:HEM801 2.0 9.3 1.0
NA A:HEM801 2.0 11.5 1.0
NC A:HEM801 2.0 10.4 1.0
NB A:HEM801 2.1 10.4 1.0
NE2 A:HIS279 2.2 13.2 1.0
O2 A:TOX111 2.6 15.0 0.6
C1D A:HEM801 2.9 9.2 1.0
C4D A:HEM801 3.0 9.3 1.0
C1A A:HEM801 3.0 10.3 1.0
C1B A:HEM801 3.0 11.1 1.0
C4C A:HEM801 3.0 10.0 1.0
C4A A:HEM801 3.0 11.4 1.0
C1C A:HEM801 3.1 10.0 1.0
CD2 A:HIS279 3.1 12.5 1.0
C4B A:HEM801 3.1 10.3 1.0
CE1 A:HIS279 3.2 12.8 1.0
CHA A:HEM801 3.3 10.2 1.0
CHD A:HEM801 3.4 9.2 1.0
CHB A:HEM801 3.4 10.4 1.0
CHC A:HEM801 3.5 10.2 1.0
O1 A:TOX111 3.6 14.8 0.7
O1 A:OXY804 4.1 43.5 1.0
C3D A:HEM801 4.2 10.1 1.0
C2D A:HEM801 4.2 9.8 1.0
C2A A:HEM801 4.2 11.3 1.0
C2B A:HEM801 4.2 11.4 1.0
CG A:HIS279 4.3 12.2 1.0
C2C A:HEM801 4.3 9.8 1.0
ND1 A:HIS279 4.3 12.6 1.0
C3C A:HEM801 4.3 10.4 1.0
C3A A:HEM801 4.3 11.0 1.0
NE1 A:TOX111 4.3 13.2 1.0
O2 A:TOX111 4.3 13.2 0.1
C3B A:HEM801 4.3 10.4 1.0
CD1 A:TOX111 4.5 12.2 1.0
O A:HOH1012 4.9 34.5 1.0

Iron binding site 2 out of 2 in 5syv

Go back to Iron Binding Sites List in 5syv
Iron binding site 2 out of 2 in the Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Crystal Structure of Burkholderia Pseudomallei Katg N240D Variant within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe801

b:13.5
occ:1.00
FE B:HEM801 0.0 13.5 1.0
ND B:HEM801 1.9 12.1 1.0
NA B:HEM801 2.0 12.8 1.0
NC B:HEM801 2.0 13.1 1.0
NB B:HEM801 2.1 14.1 1.0
NE2 B:HIS279 2.2 14.6 1.0
O2 B:TOX111 2.6 16.8 0.8
C1D B:HEM801 3.0 11.8 1.0
C4D B:HEM801 3.0 11.7 1.0
C1A B:HEM801 3.0 12.5 1.0
C4A B:HEM801 3.0 13.1 1.0
C1C B:HEM801 3.0 12.5 1.0
C4B B:HEM801 3.1 13.1 1.0
C4C B:HEM801 3.1 11.5 1.0
C1B B:HEM801 3.1 13.4 1.0
CD2 B:HIS279 3.2 14.9 1.0
CE1 B:HIS279 3.2 13.4 1.0
CHC B:HEM801 3.4 12.5 1.0
CHA B:HEM801 3.4 12.4 1.0
O1 B:TOX111 3.5 18.7 1.0
CHB B:HEM801 3.5 13.2 1.0
CHD B:HEM801 3.5 11.5 1.0
NE1 B:TOX111 4.2 13.3 1.0
C3D B:HEM801 4.2 11.9 1.0
C3A B:HEM801 4.2 12.5 1.0
C2D B:HEM801 4.2 11.2 1.0
C2A B:HEM801 4.2 11.7 1.0
C2C B:HEM801 4.3 11.4 1.0
C3C B:HEM801 4.3 11.8 1.0
ND1 B:HIS279 4.3 14.0 1.0
C3B B:HEM801 4.3 13.4 1.0
C2B B:HEM801 4.3 13.8 1.0
CG B:HIS279 4.3 14.7 1.0
CD1 B:TOX111 4.4 13.5 1.0
O1 B:OXY804 4.6 25.0 1.0
O B:HOH1188 4.8 28.2 1.0

Reference:

M.Machuqueiro, B.Victor, J.Switala, J.Villanueva, C.Rovira, I.Fita, P.C.Loewen. The Catalase Activity of Catalase-Peroxidases Is Modulated By Changes in the Pka of the Distal Histidine. Biochemistry V. 56 2271 2017.
ISSN: ISSN 1520-4995
PubMed: 28409923
DOI: 10.1021/ACS.BIOCHEM.6B01276
Page generated: Tue Aug 6 08:51:48 2024

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