Atomistry » Iron » PDB 1q5e-1qom » 1qo4
Atomistry »
  Iron »
    PDB 1q5e-1qom »
      1qo4 »

Iron in PDB 1qo4: Arabidopsis Thaliana Peroxidase A2 at Room Temperature

Enzymatic activity of Arabidopsis Thaliana Peroxidase A2 at Room Temperature

All present enzymatic activity of Arabidopsis Thaliana Peroxidase A2 at Room Temperature:
1.11.1.7;

Protein crystallography data

The structure of Arabidopsis Thaliana Peroxidase A2 at Room Temperature, PDB code: 1qo4 was solved by A.Henriksen, M.Gajhede, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 30.00 / 3.00
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 46.290, 74.848, 80.794, 90.00, 90.00, 90.00
R / Rfree (%) 18.3 / 23.5

Other elements in 1qo4:

The structure of Arabidopsis Thaliana Peroxidase A2 at Room Temperature also contains other interesting chemical elements:

Calcium (Ca) 2 atoms

Iron Binding Sites:

The binding sites of Iron atom in the Arabidopsis Thaliana Peroxidase A2 at Room Temperature (pdb code 1qo4). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total only one binding site of Iron was determined in the Arabidopsis Thaliana Peroxidase A2 at Room Temperature, PDB code: 1qo4:

Iron binding site 1 out of 1 in 1qo4

Go back to Iron Binding Sites List in 1qo4
Iron binding site 1 out of 1 in the Arabidopsis Thaliana Peroxidase A2 at Room Temperature


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Arabidopsis Thaliana Peroxidase A2 at Room Temperature within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe374

b:15.0
occ:1.00
FE A:HEM374 0.0 15.0 1.0
NA A:HEM374 2.0 15.0 1.0
NB A:HEM374 2.0 15.0 1.0
ND A:HEM374 2.0 15.0 1.0
NC A:HEM374 2.0 15.0 1.0
NE2 A:HIS169 2.3 15.0 1.0
C4B A:HEM374 3.0 15.0 1.0
C4A A:HEM374 3.0 15.0 1.0
C4D A:HEM374 3.0 15.0 1.0
C1A A:HEM374 3.0 15.0 1.0
C1C A:HEM374 3.0 15.0 1.0
C1B A:HEM374 3.0 15.0 1.0
C1D A:HEM374 3.1 15.0 1.0
C4C A:HEM374 3.1 15.0 1.0
CD2 A:HIS169 3.2 15.0 1.0
CE1 A:HIS169 3.2 15.0 1.0
CHC A:HEM374 3.4 15.0 1.0
CHA A:HEM374 3.4 15.0 1.0
CHB A:HEM374 3.4 15.0 1.0
CHD A:HEM374 3.5 15.0 1.0
O A:HOH2011 4.0 15.0 1.0
C2C A:HEM374 4.2 15.0 1.0
C3D A:HEM374 4.3 15.0 1.0
C2D A:HEM374 4.3 15.0 1.0
C2A A:HEM374 4.3 15.0 1.0
C2B A:HEM374 4.3 15.0 1.0
C3A A:HEM374 4.3 15.0 1.0
C3B A:HEM374 4.3 15.0 1.0
C3C A:HEM374 4.3 15.0 1.0
CG A:HIS169 4.4 15.0 1.0
ND1 A:HIS169 4.4 15.0 1.0
CE2 A:PHE41 4.5 15.0 1.0
NE A:ARG38 4.5 15.0 1.0
CD2 A:PHE41 4.7 15.0 1.0
CG A:ARG38 4.9 15.0 1.0
CD A:ARG38 4.9 15.0 1.0

Reference:

K.L.Nielsen, C.Indiani, A.Henriksen, A.Feis, M.Becucci, M.Gajhede, G.Smulevich, K.G.Welinder. Differential Activity and Structure of Highly Similar Peroxidases. Spectroscopic, Crystallographic, and Enzymatic Analyses of Lignifying Arabidopsis Thaliana Peroxidase A2 and Horseradish Peroxidase A2 Biochemistry V. 40 11013 2001.
ISSN: ISSN 0006-2960
PubMed: 11551197
DOI: 10.1021/BI010661O
Page generated: Sun Dec 13 14:29:40 2020

Last articles

Zn in 8WB0
Zn in 8WAX
Zn in 8WAU
Zn in 8WAZ
Zn in 8WAY
Zn in 8WAV
Zn in 8WAW
Zn in 8WAT
Zn in 8W7M
Zn in 8WD3
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy