Iron in PDB 7oqr: Crystal Structure of Trypanosoma Cruzi Peroxidase

Enzymatic activity of Crystal Structure of Trypanosoma Cruzi Peroxidase

All present enzymatic activity of Crystal Structure of Trypanosoma Cruzi Peroxidase:
1.11.1.11;

Protein crystallography data

The structure of Crystal Structure of Trypanosoma Cruzi Peroxidase, PDB code: 7oqr was solved by S.L.Freeman, H.Kwon, V.Skafar, A.J.Fielding, A.Martinez, L.Piacenza, R.Radi, E.L.Raven, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 29.28 / 1.76
Space group P 31 2 1
Cell size a, b, c (Å), α, β, γ (°) 71.594, 71.594, 254.581, 90, 90, 120
R / Rfree (%) 11.8 / 15.9

Other elements in 7oqr:

The structure of Crystal Structure of Trypanosoma Cruzi Peroxidase also contains other interesting chemical elements:

Sodium (Na) 4 atoms

Iron Binding Sites:

The binding sites of Iron atom in the Crystal Structure of Trypanosoma Cruzi Peroxidase (pdb code 7oqr). 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 Trypanosoma Cruzi Peroxidase, PDB code: 7oqr:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 7oqr

Go back to Iron Binding Sites List in 7oqr
Iron binding site 1 out of 2 in the Crystal Structure of Trypanosoma Cruzi Peroxidase


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 Trypanosoma Cruzi Peroxidase within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe401

b:20.3
occ:1.00
FE A:HEM401 0.0 20.3 1.0
ND A:HEM401 1.9 18.6 1.0
NA A:HEM401 2.0 19.5 1.0
NC A:HEM401 2.0 19.4 1.0
NB A:HEM401 2.1 20.2 1.0
NE2 A:HIS217 2.1 26.9 1.0
O A:HOH656 2.5 22.6 1.0
C4C A:HEM401 2.9 19.4 1.0
C1D A:HEM401 3.0 17.7 1.0
C4D A:HEM401 3.0 18.7 1.0
C1A A:HEM401 3.0 20.2 1.0
C4B A:HEM401 3.0 17.6 1.0
C4A A:HEM401 3.0 21.9 1.0
C1B A:HEM401 3.0 18.3 1.0
C1C A:HEM401 3.1 20.5 1.0
CD2 A:HIS217 3.1 25.0 1.0
CE1 A:HIS217 3.2 31.7 1.0
CHD A:HEM401 3.3 17.5 1.0
CHB A:HEM401 3.4 22.1 1.0
CHC A:HEM401 3.4 16.3 1.0
CHA A:HEM401 3.4 18.2 1.0
NE1 A:TRP92 4.2 20.5 1.0
C3C A:HEM401 4.2 19.9 1.0
C2A A:HEM401 4.2 21.5 1.0
C2C A:HEM401 4.2 20.1 1.0
C3A A:HEM401 4.2 17.3 1.0
O A:HOH621 4.2 27.9 1.0
C3D A:HEM401 4.3 19.6 1.0
C3B A:HEM401 4.3 19.9 1.0
CG A:HIS217 4.3 22.4 1.0
C2D A:HEM401 4.3 16.1 1.0
C2B A:HEM401 4.3 19.0 1.0
ND1 A:HIS217 4.3 26.9 1.0
CD1 A:TRP92 4.7 22.6 1.0
O A:HOH636 4.8 45.5 1.0

Iron binding site 2 out of 2 in 7oqr

Go back to Iron Binding Sites List in 7oqr
Iron binding site 2 out of 2 in the Crystal Structure of Trypanosoma Cruzi Peroxidase


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 Trypanosoma Cruzi Peroxidase within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe401

b:20.2
occ:1.00
FE B:HEM401 0.0 20.2 1.0
ND B:HEM401 1.9 22.4 1.0
NA B:HEM401 2.0 20.4 1.0
O2 B:OXY405 2.0 33.0 1.0
NB B:HEM401 2.0 19.3 1.0
NC B:HEM401 2.1 22.2 1.0
NE2 B:HIS217 2.2 21.8 1.0
C4D B:HEM401 2.9 20.3 1.0
C1A B:HEM401 3.0 20.6 1.0
C4C B:HEM401 3.0 20.4 1.0
C1D B:HEM401 3.0 19.9 1.0
C1B B:HEM401 3.0 21.8 1.0
C4A B:HEM401 3.0 19.6 1.0
C4B B:HEM401 3.0 19.9 1.0
C1C B:HEM401 3.1 22.4 1.0
CE1 B:HIS217 3.2 28.0 1.0
O1 B:OXY405 3.2 32.4 1.0
CD2 B:HIS217 3.2 23.5 1.0
CHA B:HEM401 3.3 21.0 1.0
CHB B:HEM401 3.4 20.0 1.0
CHD B:HEM401 3.4 15.2 1.0
CHC B:HEM401 3.5 21.9 1.0
C3C B:HEM401 4.2 23.1 1.0
C2A B:HEM401 4.2 21.7 1.0
C3D B:HEM401 4.2 17.7 1.0
C3A B:HEM401 4.2 22.2 1.0
C2D B:HEM401 4.2 19.1 1.0
NE1 B:TRP92 4.2 20.8 1.0
C2C B:HEM401 4.2 17.8 1.0
C2B B:HEM401 4.3 17.2 1.0
ND1 B:HIS217 4.3 23.9 1.0
C3B B:HEM401 4.3 21.8 1.0
O B:HOH645 4.3 23.0 1.0
CG B:HIS217 4.3 23.0 1.0
O B:HOH513 4.6 32.2 1.0
CD1 B:TRP92 4.6 22.3 1.0

Reference:

S.L.Freeman, V.Skafar, H.Kwon, A.J.Fielding, P.C.E.Moody, A.Martinez, F.M.Issoglio, L.Inchausti, P.Smircich, A.Zeida, L.Piacenza, R.Radi, E.L.Raven. Crystal Structure of Trypanosoma Cruzi Heme Peroxidase and Characterization of Its Substrate Specificity and Compound I Intermediate. J.Biol.Chem. V. 298 02204 2022.
ISSN: ESSN 1083-351X
PubMed: 35772495
DOI: 10.1016/J.JBC.2022.102204
Page generated: Thu Aug 8 14:45:23 2024

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