Atomistry » Iron » PDB 1gwf-1h5f » 1h57
Atomistry »
  Iron »
    PDB 1gwf-1h5f »
      1h57 »

Iron in PDB 1h57: Structure of Horseradish Peroxidase C1A Compound III

Enzymatic activity of Structure of Horseradish Peroxidase C1A Compound III

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

Protein crystallography data

The structure of Structure of Horseradish Peroxidase C1A Compound III, PDB code: 1h57 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) 33.18 / 1.6
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 40.340, 67.227, 117.552, 90.00, 90.00, 90.00
R / Rfree (%) 17.6 / 19.6

Other elements in 1h57:

The structure of Structure of Horseradish Peroxidase C1A Compound III 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 III (pdb code 1h57). 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 III, PDB code: 1h57:

Iron binding site 1 out of 1 in 1h57

Go back to Iron Binding Sites List in 1h57
Iron binding site 1 out of 1 in the Structure of Horseradish Peroxidase C1A Compound III


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 III within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe350

b:8.3
occ:1.00
FE A:HEM350 0.0 8.3 1.0
O1 A:OXY500 1.8 11.0 0.9
NA A:HEM350 2.0 8.7 1.0
ND A:HEM350 2.0 8.1 1.0
NB A:HEM350 2.0 7.5 1.0
NC A:HEM350 2.0 7.5 1.0
NE2 A:HIS170 2.1 7.8 1.0
O2 A:OXY500 2.8 16.7 0.9
C1A A:HEM350 3.0 9.9 1.0
C4A A:HEM350 3.0 9.8 1.0
C1D A:HEM350 3.0 9.6 1.0
C1B A:HEM350 3.0 7.9 1.0
C4D A:HEM350 3.1 9.1 1.0
C4B A:HEM350 3.1 7.3 1.0
C1C A:HEM350 3.1 7.4 1.0
C4C A:HEM350 3.1 8.4 1.0
CD2 A:HIS170 3.1 8.6 1.0
CE1 A:HIS170 3.1 8.7 1.0
CHB A:HEM350 3.4 8.3 1.0
CHA A:HEM350 3.4 9.5 1.0
CHC A:HEM350 3.4 8.2 1.0
CHD A:HEM350 3.4 8.9 1.0
ND1 A:HIS170 4.2 7.4 1.0
CG A:HIS170 4.3 8.2 1.0
C2D A:HEM350 4.3 8.7 1.0
C2B A:HEM350 4.3 7.9 1.0
C3A A:HEM350 4.3 8.0 1.0
C3D A:HEM350 4.3 8.2 1.0
C2A A:HEM350 4.3 9.9 1.0
NE A:ARG38 4.3 12.4 1.0
C3B A:HEM350 4.3 8.0 1.0
C2C A:HEM350 4.3 8.0 1.0
C3C A:HEM350 4.3 8.5 1.0
CE2 A:PHE41 4.4 8.3 1.0
CD2 A:PHE41 4.7 8.4 1.0
CG A:ARG38 4.7 12.3 1.0
CD A:ARG38 4.8 11.3 1.0
CZ A:PHE221 5.0 9.3 1.0
O A:HOH2210 5.0 22.8 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 07:01:50 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy