Atomistry » Iron » PDB 1h5g-1hdb » 1hch
Atomistry »
  Iron »
    PDB 1h5g-1hdb »
      1hch »

Iron in PDB 1hch: Structure of Horseradish Peroxidase C1A Compound I

Enzymatic activity of Structure of Horseradish Peroxidase C1A Compound I

All present enzymatic activity of Structure of Horseradish Peroxidase C1A Compound I:
1.11.1.7;

Protein crystallography data

The structure of Structure of Horseradish Peroxidase C1A Compound I, PDB code: 1hch was solved by G.I.Berglund, G.H.Carlsson, J.Hajdu, A.T.Smith, H.Szoke, A.Henriksen, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 29.78 / 1.57
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 40.282, 67.464, 117.106, 90.00, 90.00, 90.00
R / Rfree (%) 17.9 / 20.3

Other elements in 1hch:

The structure of Structure of Horseradish Peroxidase C1A Compound I also contains other interesting chemical elements:

Calcium (Ca) 2 atoms

Iron Binding Sites:

The binding sites of Iron atom in the Structure of Horseradish Peroxidase C1A Compound I (pdb code 1hch). 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 Structure of Horseradish Peroxidase C1A Compound I, PDB code: 1hch:

Iron binding site 1 out of 1 in 1hch

Go back to Iron Binding Sites List in 1hch
Iron binding site 1 out of 1 in the Structure of Horseradish Peroxidase C1A Compound I


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Structure of Horseradish Peroxidase C1A Compound I within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe350

b:5.2
occ:1.00
FE A:HEM350 0.0 5.2 1.0
O A:O500 1.7 6.5 1.0
ND A:HEM350 2.0 4.7 1.0
NC A:HEM350 2.0 4.5 1.0
NA A:HEM350 2.0 4.7 1.0
NB A:HEM350 2.0 3.8 1.0
NE2 A:HIS170 2.1 4.4 1.0
C1D A:HEM350 3.0 5.6 1.0
C1C A:HEM350 3.0 4.5 1.0
C4C A:HEM350 3.1 5.0 1.0
C4D A:HEM350 3.1 6.0 1.0
C4B A:HEM350 3.1 5.0 1.0
C4A A:HEM350 3.1 5.5 1.0
C1A A:HEM350 3.1 6.4 1.0
C1B A:HEM350 3.1 5.0 1.0
CE1 A:HIS170 3.1 6.4 1.0
CD2 A:HIS170 3.1 7.0 1.0
CHC A:HEM350 3.4 4.4 1.0
CHD A:HEM350 3.4 5.1 1.0
CHA A:HEM350 3.4 6.4 1.0
CHB A:HEM350 3.4 5.7 1.0
O A:HOH2427 4.0 9.6 1.0
NE A:ARG38 4.2 6.4 1.0
ND1 A:HIS170 4.2 5.2 1.0
C2D A:HEM350 4.3 7.0 1.0
C3D A:HEM350 4.3 6.2 1.0
CG A:HIS170 4.3 6.4 1.0
C2C A:HEM350 4.3 5.2 1.0
C2B A:HEM350 4.3 5.6 1.0
C2A A:HEM350 4.3 6.3 1.0
C3A A:HEM350 4.3 5.2 1.0
C3C A:HEM350 4.3 5.2 1.0
C3B A:HEM350 4.3 5.8 1.0
CE2 A:PHE41 4.4 6.6 1.0
CG A:ARG38 4.6 6.8 1.0
CD A:ARG38 4.7 5.6 1.0
CD2 A:PHE41 4.7 6.0 1.0
CZ A:PHE221 5.0 5.2 1.0
CZ A:ARG38 5.0 4.9 1.0

Reference:

G.I.Berglund, G.H.Carlsson, A.T.Smith, H.Szoke, A.Henriksen, J.Hajdu. The Catalytic Pathway of Horseradish Peroxidase at High Resolution Nature V. 417 463 2002.
ISSN: ISSN 0028-0836
PubMed: 12024218
DOI: 10.1038/417463A
Page generated: Sat Aug 3 07:24:02 2024

Last articles

Zn in 9JPJ
Zn in 9JP7
Zn in 9JPK
Zn in 9JPL
Zn in 9GN6
Zn in 9GN7
Zn in 9GKU
Zn in 9GKW
Zn in 9GKX
Zn in 9GL0
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy