Iron in PDB 1mn2: Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N

All present enzymatic activity of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N:
1.11.1.13;

The structure of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N, PDB code: 1mn2 was solved by M.Sundaramoorthy, T.L.Poulos, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	8.00 / 2.00
Space group	C 1 2 1
Cell size a, b, c (Å), α, β, γ (°)	163.240, 45.970, 53.570, 90.00, 97.16, 90.00
R / Rfree (%)	18.7 / n/a

The structure of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N also contains other interesting chemical elements:

Calcium

(Ca)

2 atoms

The binding sites of Iron atom in the Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N (pdb code 1mn2). 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 Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N, PDB code: 1mn2:

Iron binding site 1 out of 1 in the Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N within 5.0Å range: probe atom residue distance (Å) B Occ A:Fe396 b:9.6 occ:1.00 FE A:HEM396 0.0 9.6 1.0 NB A:HEM396 2.0 7.0 1.0 NC A:HEM396 2.0 7.7 1.0 ND A:HEM396 2.0 7.3 1.0 NA A:HEM396 2.0 6.5 1.0 NE2 A:HIS173 2.4 6.4 1.0 O A:HOH556 2.7 25.9 1.0 C1C A:HEM396 3.0 6.2 1.0 C4B A:HEM396 3.0 8.2 1.0 C4D A:HEM396 3.1 7.8 1.0 C1B A:HEM396 3.1 7.2 1.0 C4A A:HEM396 3.1 7.1 1.0 C4C A:HEM396 3.1 7.3 1.0 C1A A:HEM396 3.1 6.0 1.0 C1D A:HEM396 3.1 6.8 1.0 CD2 A:HIS173 3.3 7.2 1.0 CE1 A:HIS173 3.3 6.5 1.0 CHC A:HEM396 3.4 6.7 1.0 CHB A:HEM396 3.4 6.1 1.0 CHA A:HEM396 3.4 5.6 1.0 CHD A:HEM396 3.4 7.6 1.0 C2C A:HEM396 4.3 7.5 1.0 C3D A:HEM396 4.3 8.0 1.0 C3B A:HEM396 4.3 9.1 1.0 C2B A:HEM396 4.3 8.0 1.0 C2D A:HEM396 4.3 6.7 1.0 C3C A:HEM396 4.3 7.2 1.0 C3A A:HEM396 4.3 8.0 1.0 C2A A:HEM396 4.3 6.4 1.0 CG A:HIS173 4.5 7.4 1.0 ND1 A:HIS173 4.5 5.7 1.0 NE A:ARG42 4.5 11.5 1.0 CG A:ARG42 4.9 4.3 1.0 CD2 A:PHE45 5.0 7.7 1.0 CE2 A:PHE45 5.0 7.9 1.0

M.Sundaramoorthy, K.Kishi, M.H.Gold, T.L.Poulos. Crystal Structures of Substrate Binding Site Mutants of Manganese Peroxidase. J.Biol.Chem. V. 272 17574 1997.
ISSN: ISSN 0021-9258
PubMed: 9211904
DOI: 10.1074/JBC.272.28.17574