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Iron in PDB 6el4: Direct-Evolutioned Unspecific Peroxygenase From Agrocybe Aegerita, in Complex with Veratryl Alcohol

Enzymatic activity of Direct-Evolutioned Unspecific Peroxygenase From Agrocybe Aegerita, in Complex with Veratryl Alcohol

All present enzymatic activity of Direct-Evolutioned Unspecific Peroxygenase From Agrocybe Aegerita, in Complex with Veratryl Alcohol:
1.11.2.1;

Protein crystallography data

The structure of Direct-Evolutioned Unspecific Peroxygenase From Agrocybe Aegerita, in Complex with Veratryl Alcohol, PDB code: 6el4 was solved by M.Ramirez-Escudero, J.Sanz-Aparicio, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 48.04 / 1.53
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 51.074, 57.982, 60.923, 90.00, 109.85, 90.00
R / Rfree (%) 15.4 / 16.7

Other elements in 6el4:

The structure of Direct-Evolutioned Unspecific Peroxygenase From Agrocybe Aegerita, in Complex with Veratryl Alcohol also contains other interesting chemical elements:

Magnesium (Mg) 1 atom
Chlorine (Cl) 1 atom

Iron Binding Sites:

The binding sites of Iron atom in the Direct-Evolutioned Unspecific Peroxygenase From Agrocybe Aegerita, in Complex with Veratryl Alcohol (pdb code 6el4). 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 Direct-Evolutioned Unspecific Peroxygenase From Agrocybe Aegerita, in Complex with Veratryl Alcohol, PDB code: 6el4:

Iron binding site 1 out of 1 in 6el4

Go back to Iron Binding Sites List in 6el4
Iron binding site 1 out of 1 in the Direct-Evolutioned Unspecific Peroxygenase From Agrocybe Aegerita, in Complex with Veratryl Alcohol


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Direct-Evolutioned Unspecific Peroxygenase From Agrocybe Aegerita, in Complex with Veratryl Alcohol within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe401

b:11.0
occ:1.00
 FE A:HEM401 0.0 11.0 1.0
ND A:HEM401 1.9 11.0 1.0
OAC A:VOH413 1.9 22.7 0.8
NA A:HEM401 2.0 11.2 1.0
NC A:HEM401 2.1 11.3 1.0
NB A:HEM401 2.1 11.3 1.0
SG A:CYS36 2.6 9.8 1.0
C4D A:HEM401 2.9 11.3 1.0
C1D A:HEM401 2.9 11.2 1.0
C1A A:HEM401 2.9 11.4 1.0
C4C A:HEM401 3.0 11.3 1.0
C4A A:HEM401 3.0 11.3 1.0
CAG A:VOH413 3.0 23.9 0.8
C1B A:HEM401 3.1 11.8 1.0
C4B A:HEM401 3.1 11.9 1.0
C1C A:HEM401 3.1 11.7 1.0
CHA A:HEM401 3.3 11.1 1.0
CHD A:HEM401 3.4 11.3 1.0
CHB A:HEM401 3.5 11.8 1.0
CHC A:HEM401 3.5 11.7 1.0
CB A:CYS36 3.7 9.9 1.0
CAJ A:VOH413 4.0 24.6 0.8
C3D A:HEM401 4.1 11.6 1.0
C2D A:HEM401 4.1 11.4 1.0
C2A A:HEM401 4.1 11.6 1.0
CAD A:VOH413 4.2 25.1 0.8
C3A A:HEM401 4.2 11.5 1.0
C3C A:HEM401 4.2 11.9 1.0
C2C A:HEM401 4.3 11.7 1.0
C2B A:HEM401 4.3 12.0 1.0
C3B A:HEM401 4.3 12.0 1.0
CA A:CYS36 4.4 10.0 1.0
CE2 A:PHE199 4.7 12.2 1.0
CD2 A:PHE199 4.7 12.2 1.0
CG A:GLU196 4.8 12.2 0.5

Reference:

M.Ramirez-Escudero, P.Molina-Espeja, P.Gomez De Santos, M.Hofrichter, J.Sanz-Aparicio, M.Alcalde. Structural Insights Into the Substrate Promiscuity of A Laboratory-Evolved Peroxygenase. Acs Chem.Biol. V. 13 3259 2018.
ISSN: ESSN 1554-8937
PubMed: 30376293
DOI: 10.1021/ACSCHEMBIO.8B00500
Page generated: Wed Aug 6 05:42:26 2025

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